Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56001 |
|---|---|
| ensemblid | ENSG00000269405.7 |
| hgncid | 8072 |
| symbol | NXF2 |
| name | nuclear RNA export factor 2 |
| refseq_nuc | NM_022053.4 |
| refseq_prot | NP_071336.1 |
| ensembl_nuc | ENST00000625106.4 |
| ensembl_prot | ENSP00000485586.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 102247167 |
| end | 102326722 |
| strand | + |
| ver | v1.2 |
| region | chrX:102247167-102326722 |
| region5000 | chrX:102242167-102331722 |
| regionname0 | NXF2_chrX_102247167_102326722 |
| regionname5000 | NXF2_chrX_102242167_102331722 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 626 | 38 | 12 | 8 | 11 | 3 | 4 | 4 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 456 | 35 | 12 | 6 | 11 | 3 | 3 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| t0002 | 0/0 | 454 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| t0003 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| t0004 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1881 | 33 | 10 | 7 | 11 | 2 | 3 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| a0001c0002 | 0/0 | 1881 | 5 | 2 | 1 | 0 | 1 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2336 | 31 | 10 | 6 | 11 | 2 | 2 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| a0001c0001t0002 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| a0001c0001t0004 | 0/0 | 2336 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| a0001c0002t0001 | 0/0 | 2336 | 4 | 2 | 0 | 0 | 1 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| a0001c0002t0003 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | copy fasta | chrX | 102242167 | 102331722 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0036 | AMR | CLM | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NXF2_chrX_102242167_102331722 | NXF2 | chrX | 102242167 | 102331722 |
| 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 |
|---|
| 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:102326490
|
G | A | 1 | a0001c0002 | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.1857G>A | p.Ala619Ala | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 23/23 | 2104/2336 | 1857/1881 | 619/626 | chrX | 102326490 |
| 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:102307027
|
AT | A | 1 | a0001c0001t0002 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/23 | 49 | INFO_REALIGN_3_PRIME | chrX | 102307027 | ||||
| chrX:102307030
|
TC | T | 1 | a0001c0002t0003 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/23 | 47 | INFO_REALIGN_3_PRIME | chrX | 102307030 | ||||
| chrX:102307064
|
CA | C | 1 | a0001c0001t0002 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/23 | 12 | INFO_REALIGN_3_PRIME | chrX | 102307064 | ||||
| chrX:102307071
|
A | C | 1 | a0001c0001t0002 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/23 | 8 | chrX | 102307071 | |||||
| chrX:102326608
|
T | G | 1 | a0001c0001t0004 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 23/23 | 94 | chrX | 102326608 |
| 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:102247290
|
CT | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG00738.hp1 HG01433.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176+78delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247290 | |||||
| chrX:102247290
|
CTT | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 18 | HG00621.hp2 HG00642.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176+77_-176+78del others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247290 | |||||
| chrX:102247290
|
CTTT | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(5): Show | 8 | HG00280.hp2 HG02129.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-176+76_-176+78del others(3): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247290 | |||||
| chrX:102247290
|
CTTTT | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-176+75_-176+78del others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247290 | |||||
| chrX:102247353
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-176+115G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | chrX | 102247353 | ||||||
| chrX:102247528
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-176+290C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | chrX | 102247528 | ||||||
| chrX:102247576
|
C | CG | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-176+339dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247576 | |||||
| chrX:102247708
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-176+472delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247708 | |||||
| chrX:102247906
|
T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-175-530dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247906 | |||||
| chrX:102247938
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-175-499T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | chrX | 102247938 | ||||||
| chrX:102247951
|
T | TA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-175-481dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chrX | 102247951 | |||||
| chrX:102248560
|
T | TA | 20 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(17): Show | 20 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.-54+3dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102248560 | |||||
| chrX:102248812
|
G | GC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+256dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102248812 | |||||
| chrX:102249588
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+1030T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102249588 | ||||||
| chrX:102249596
|
AG | A | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+1040delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102249596 | |||||
| chrX:102250299
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-54+1741G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102250299 | ||||||
| chrX:102250468
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+1914delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102250468 | |||||
| chrX:102250535
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-54+1977A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102250535 | ||||||
| chrX:102250813
|
ACAG | A | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+2258_-54+2260d others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102250813 | |||||
| chrX:102250876
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+2318T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102250876 | ||||||
| chrX:102251212
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+2654G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102251212 | ||||||
| chrX:102251336
|
AT | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-54+2795delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102251336 | |||||
| chrX:102251336
|
ATT | A | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+2794_-54+2795d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102251336 | |||||
| chrX:102251392
|
A | G | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+2834A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102251392 | ||||||
| chrX:102251481
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+2923T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102251481 | ||||||
| chrX:102251486
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-54+2928A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102251486 | ||||||
| chrX:102251576
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG00642.hp2 HG01952.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+3018G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102251576 | ||||||
| chrX:102251965
|
A | ATGTTTTG others(8): Show |
8 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(5): Show | 8 | HG01433.hp2 HG02040.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54+3419_-54+3433d others(17): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102251965 | |||||
| chrX:102252030
|
T | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG01433.hp2 HG02040.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+3472T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102252030 | ||||||
| chrX:102252287
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+3734delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102252287 | |||||
| chrX:102252288
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+3730C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102252288 | ||||||
| chrX:102252416
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0008 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-54+3858C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102252416 | ||||||
| chrX:102252630
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-54+4072T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102252630 | ||||||
| chrX:102252829
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG01099.hp1 HG01433.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+4271G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102252829 | ||||||
| chrX:102253547
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+4989A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253547 | ||||||
| chrX:102253588
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-54+5030A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253588 | ||||||
| chrX:102253771
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+5213T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253771 | ||||||
| chrX:102253797
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(24): Show | 27 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-54+5239T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253797 | ||||||
| chrX:102253809
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+5251A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253809 | ||||||
| chrX:102253841
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+5283C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102253841 | ||||||
| chrX:102254416
|
GA | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(18): Show | 21 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.-54+5868delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102254416 | |||||
| chrX:102254638
|
C | CT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+6085dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102254638 | |||||
| chrX:102254787
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(26): Show | 29 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-54+6229C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102254787 | ||||||
| chrX:102255177
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+6619A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102255177 | ||||||
| chrX:102255283
|
AT | A | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-54+6731delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102255283 | |||||
| chrX:102255676
|
T | TG | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+7119dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102255676 | |||||
| chrX:102255751
|
GTT | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG01433.hp2 HG02040.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+7195_-54+7196d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102255751 | |||||
| chrX:102255804
|
T | TTG | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+7246_-54+7247i others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102255804 | ||||||
| chrX:102255805
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+7247G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102255805 | ||||||
| chrX:102255842
|
T | TATTC | 8 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+7312_-54+7315d others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102255842 | |||||
| chrX:102255842
|
TATTCATT others(1): Show |
T | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-54+7308_-54+7315d others(10): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102255842 | |||||
| chrX:102255972
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+7414C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102255972 | ||||||
| chrX:102256216
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+7661delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256216 | |||||
| chrX:102256378
|
CT | C | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+7822delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256378 | |||||
| chrX:102256451
|
A | AT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+7899dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256451 | |||||
| chrX:102256610
|
GC | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8054delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256610 | |||||
| chrX:102256829
|
CT | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8275delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256829 | |||||
| chrX:102256940
|
TA | T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8389delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102256940 | |||||
| chrX:102256942
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-54+8384A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102256942 | ||||||
| chrX:102257003
|
GT | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8450delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257003 | |||||
| chrX:102257010
|
A | AC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8457dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257010 | |||||
| chrX:102257048
|
G | GA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8501dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257048 | |||||
| chrX:102257048
|
GA | G | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-54+8501delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257048 | |||||
| chrX:102257117
|
C | CT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8566dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257117 | |||||
| chrX:102257282
|
CA | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8727delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257282 | |||||
| chrX:102257335
|
G | GT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8780dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257335 | |||||
| chrX:102257370
|
AG | A | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8815delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257370 | |||||
| chrX:102257407
|
G | GT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8854dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257407 | |||||
| chrX:102257474
|
G | GT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+8921dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257474 | |||||
| chrX:102257474
|
GT | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+8921delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257474 | |||||
| chrX:102257577
|
G | GC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+9020dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257577 | |||||
| chrX:102257645
|
CT | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9092delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257645 | |||||
| chrX:102257727
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9171delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257727 | |||||
| chrX:102257776
|
GA | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9221delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257776 | |||||
| chrX:102257792
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+9234G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102257792 | ||||||
| chrX:102257803
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+9245T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102257803 | ||||||
| chrX:102257892
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+9338dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257892 | |||||
| chrX:102257926
|
TC | T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+9371delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257926 | |||||
| chrX:102257937
|
TTG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9380_-54+9381d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102257937 | ||||||
| chrX:102257939
|
G | GC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+9384dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257939 | |||||
| chrX:102257940
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9382C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102257940 | ||||||
| chrX:102257963
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9407delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102257963 | |||||
| chrX:102258075
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+9519dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258075 | |||||
| chrX:102258193
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+9635C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102258193 | ||||||
| chrX:102258313
|
AC | A | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9759delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258313 | |||||
| chrX:102258316
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+9758C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102258316 | ||||||
| chrX:102258325
|
T | TA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9768dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258325 | |||||
| chrX:102258389
|
A | AT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9838dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258389 | |||||
| chrX:102258472
|
T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+9915dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258472 | |||||
| chrX:102258573
|
A | AC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+10016dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258573 | |||||
| chrX:102258601
|
G | GT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10046dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258601 | |||||
| chrX:102258601
|
GT | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+10046delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258601 | |||||
| chrX:102258659
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10103delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258659 | |||||
| chrX:102258805
|
AC | A | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-54+10249delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258805 | |||||
| chrX:102258806
|
C | CCA | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG00642.hp2 HG02040.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+10288_-54+1028 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258806
|
C | CCACA | 6 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 6 | HG01099.hp1 HG01433.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+10286_-54+1028 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258806
|
C | CCACACA | 2 | a0001c0001t0001g0018a0001c0001t0002g0005 | 2 | HG01952.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-54+10284_-54+1028 others(10): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258806
|
CCA | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+10288_-54+1028 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258806
|
CCACA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(2): Show | 5 | HG02258.hp1 HG02886.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+10286_-54+1028 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258806
|
CCACACAC others(1): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0032 | 2 | NA18906.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+10282_-54+1028 others(12): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258806 | |||||
| chrX:102258828
|
A | ACACACAC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+10271_-54+1027 others(11): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258828 | |||||
| chrX:102258845
|
C | CA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+10288dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258845 | |||||
| chrX:102258846
|
A | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+10288A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102258846 | ||||||
| chrX:102258892
|
T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10335dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258892 | |||||
| chrX:102258980
|
A | AG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10424dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102258980 | |||||
| chrX:102259139
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10584delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259139 | |||||
| chrX:102259161
|
A | AT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10605dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259161 | |||||
| chrX:102259228
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10673delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259228 | |||||
| chrX:102259331
|
TC | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10777delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259331 | |||||
| chrX:102259411
|
TA | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10855delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259411 | |||||
| chrX:102259504
|
C | CT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+10948dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259504 | |||||
| chrX:102259539
|
A | AG | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+10982dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259539 | |||||
| chrX:102259612
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+11054C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102259612 | ||||||
| chrX:102259727
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+11173dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259727 | |||||
| chrX:102259877
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+11322dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102259877 | |||||
| chrX:102260021
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+11463G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102260021 | ||||||
| chrX:102260101
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(16): Show | 19 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-54+11543C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102260101 | ||||||
| chrX:102260144
|
G | GC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+11589dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102260144 | |||||
| chrX:102260334
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(30): Show | 33 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-54+11776G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102260334 | ||||||
| chrX:102260539
|
T | TA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+11984dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102260539 | |||||
| chrX:102260622
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-54+12064G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102260622 | ||||||
| chrX:102260807
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+12249G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102260807 | ||||||
| chrX:102260890
|
GA | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+12335delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102260890 | |||||
| chrX:102260925
|
TC | T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+12370delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102260925 | |||||
| chrX:102261145
|
T | TG | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+12588dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102261145 | |||||
| chrX:102261642
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+13087dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102261642 | |||||
| chrX:102261892
|
AG | A | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+13336delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102261892 | |||||
| chrX:102262023
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-54+13465A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102262023 | ||||||
| chrX:102262050
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+13495delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262050 | |||||
| chrX:102262429
|
C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-54+13871C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102262429 | ||||||
| chrX:102262507
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+13953dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262507 | |||||
| chrX:102262513
|
CTCTTT | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+13960_-54+1396 others(9): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262513 | |||||
| chrX:102262515
|
C | CT | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+13961dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262515 | |||||
| chrX:102262564
|
A | AT | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-54+14038dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATT | 2 | a0001c0001t0001g0003a0001c0001t0001g0031 | 2 | HG02129.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-54+14037_-54+1403 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTT | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-54+14036_-54+1403 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTT | 3 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01433.hp2 HG02132.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-54+14035_-54+1403 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTT | 3 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0027 | 3 | HG01106.hp2 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-54+14034_-54+1403 others(9): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTT | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(3): Show | 6 | HG02040.hp1 HG02071.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+14033_-54+1403 others(10): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT | 5 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG00642.hp2 HG02300.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+14032_-54+1403 others(11): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(1): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0004g0024 | 3 | HG01099.hp1 HG01952.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-54+14031_-54+1403 others(12): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(2): Show |
1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-54+14030_-54+1403 others(13): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0025a0001c0002t0003g0036 | 2 | HG00621.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-54+14029_-54+1403 others(14): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0001a0001c0001t0001g0016 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+14028_-54+1403 others(15): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-54+14026_-54+1403 others(17): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0033a0001c0002t0001g0038 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-54+14025_-54+1403 others(18): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(8): Show |
1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-54+14024_-54+1403 others(19): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0026a0001c0002t0001g0035 | 2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-54+14023_-54+1403 others(20): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
AT | A | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-54+14038delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262564
|
ATT | A | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-54+14037_-54+1403 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262564 | |||||
| chrX:102262688
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-54+14130C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102262688 | ||||||
| chrX:102262949
|
A | AC | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+14392dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102262949 | |||||
| chrX:102263029
|
G | GA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+14474dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102263029 | |||||
| chrX:102263126
|
C | CA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+14571dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102263126 | |||||
| chrX:102263230
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+14672A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102263230 | ||||||
| chrX:102263282
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+14724C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102263282 | ||||||
| chrX:102263358
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+14800_-54+1480 others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102263358 | ||||||
| chrX:102263519
|
C | CA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+14964dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102263519 | |||||
| chrX:102263645
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+15087A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102263645 | ||||||
| chrX:102263677
|
T | TC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-54+15120dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102263677 | |||||
| chrX:102264040
|
C | CA | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+15486dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264040 | |||||
| chrX:102264209
|
AT | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-54+15652delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102264209 | ||||||
| chrX:102264298
|
GT | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+15744delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264298 | |||||
| chrX:102264454
|
AT | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-54+15906delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264454 | |||||
| chrX:102264516
|
GC | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+15960delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264516 | |||||
| chrX:102264585
|
TC | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+16028delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102264585 | ||||||
| chrX:102264634
|
T | TA | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(5): Show | 8 | HG01433.hp2 HG02055.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+16091dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264634 | |||||
| chrX:102264634
|
T | TAA | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54+16090_-54+1609 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264634 | |||||
| chrX:102264650
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+16092C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102264650 | ||||||
| chrX:102264650
|
C | CA | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+16098dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264650 | |||||
| chrX:102264722
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-54+16164A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102264722 | ||||||
| chrX:102264812
|
C | CA | 6 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0002t0001g0034others(3): Show | 6 | HG00140.hp1 HG02129.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+16264dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102264812 | |||||
| chrX:102265109
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0008 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-54+16551A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102265109 | ||||||
| chrX:102265291
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+16733C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102265291 | ||||||
| chrX:102265610
|
C | CA | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-54+17059dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102265610 | |||||
| chrX:102266176
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-54+17618G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266176 | ||||||
| chrX:102266288
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+17730C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266288 | ||||||
| chrX:102266289
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-54+17731G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266289 | ||||||
| chrX:102266496
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+17938G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266496 | ||||||
| chrX:102266511
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(22): Show | 25 | HG00140.hp1 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-54+17953G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266511 | ||||||
| chrX:102266552
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+17994A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266552 | ||||||
| chrX:102266648
|
G | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(24): Show | 27 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-54+18090G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102266648 | ||||||
| chrX:102267162
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-54+18604A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267162 | ||||||
| chrX:102267475
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0008 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-54+18917G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267475 | ||||||
| chrX:102267652
|
A | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG00642.hp2 HG01099.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54+19094A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267652 | ||||||
| chrX:102267790
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+19232G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267790 | ||||||
| chrX:102267883
|
C | G | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+19325C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267883 | ||||||
| chrX:102267911
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(1): Show | 4 | HG00621.hp2 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+19353A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267911 | ||||||
| chrX:102267912
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-54+19354C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267912 | ||||||
| chrX:102267964
|
A | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(6): Show | 9 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+19406A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267964 | ||||||
| chrX:102267969
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(4): Show | 7 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54+19411C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267969 | ||||||
| chrX:102267972
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54+19414G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102267972 | ||||||
| chrX:102268053
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+19495C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268053 | ||||||
| chrX:102268274
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-54+19716T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268274 | ||||||
| chrX:102268320
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+19762C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268320 | ||||||
| chrX:102268438
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(10): Show | 13 | HG00280.hp2 HG00621.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-54+19880A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268438 | ||||||
| chrX:102268627
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-54+20069G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268627 | ||||||
| chrX:102268650
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01952.hp1 HG03942.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+20092C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102268650 | ||||||
| chrX:102269302
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+20744G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102269302 | ||||||
| chrX:102269302
|
G | GA | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+20745dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102269302 | |||||
| chrX:102269441
|
TA | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+20894delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102269441 | |||||
| chrX:102269620
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-54+21062A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102269620 | ||||||
| chrX:102270095
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+21537T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102270095 | ||||||
| chrX:102270201
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+21643G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102270201 | ||||||
| chrX:102270280
|
TTTTA | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018 | 3 | HG01952.hp1 HG03942.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-54+21726_-54+2172 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102270280 | |||||
| chrX:102270344
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+21786T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102270344 | ||||||
| chrX:102270980
|
G | GA | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54+22427dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102270980 | |||||
| chrX:102271060
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+22502G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102271060 | ||||||
| chrX:102271269
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+22711G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102271269 | ||||||
| chrX:102272811
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+24255dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102272811 | |||||
| chrX:102272972
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+24414T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102272972 | ||||||
| chrX:102273182
|
C | CT | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+24625dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102273182 | |||||
| chrX:102273481
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0002t0001g0034others(4): Show | 7 | HG00140.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+24923G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102273481 | ||||||
| chrX:102273732
|
A | AG | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+25176dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102273732 | |||||
| chrX:102273926
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+25368C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102273926 | ||||||
| chrX:102274177
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+25619T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274177 | ||||||
| chrX:102274470
|
GACT | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02300.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-54+25916_-54+2591 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274470 | |||||
| chrX:102274474
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54+25916A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274474 | ||||||
| chrX:102274477
|
T | A | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+25919T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274477 | ||||||
| chrX:102274478
|
C | CTTCT | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-54+25922_-54+2592 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274478 | |||||
| chrX:102274482
|
TTC | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(6): Show | 9 | HG00738.hp1 HG01358.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54+25926_-54+2592 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274482 | |||||
| chrX:102274482
|
TTCTTC | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(2): Show | 5 | HG00280.hp2 HG01106.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+25926_-54+2593 others(9): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274482 | |||||
| chrX:102274482
|
TTCTTCTT others(4): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-54+25926_-54+2593 others(15): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274482 | |||||
| chrX:102274482
|
TTCTTCTT others(13): Show |
T | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-54+25926_-54+2594 others(24): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274482 | |||||
| chrX:102274482
|
TTCTTCTT others(16): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+25926_-54+2594 others(27): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274482 | |||||
| chrX:102274510
|
TCTTCTTC others(33): Show |
T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+25966_-54+2600 others(44): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274510 | |||||
| chrX:102274512
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00280.hp2 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+25954T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274512 | ||||||
| chrX:102274513
|
TCTTCTTC others(30): Show |
T | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-54+25966_-54+2600 others(41): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274513 | |||||
| chrX:102274518
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54+25960T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274518 | ||||||
| chrX:102274521
|
TTCC | T | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+25966_-54+2596 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274521 | |||||
| chrX:102274522
|
TCCTCTTC others(21): Show |
T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01433.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-54+25966_-54+2599 others(32): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274522 | |||||
| chrX:102274524
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(15): Show | 18 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-54+25966C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274524 | ||||||
| chrX:102274528
|
TCCTCTTC others(15): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-54+25972_-54+2599 others(26): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274528 | |||||
| chrX:102274530
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(12): Show | 15 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-54+25972C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274530 | ||||||
| chrX:102274532
|
CTTCCTCT others(29): Show |
C | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-54+25975_-54+2601 others(40): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274532 | ||||||
| chrX:102274532
|
CTTCCTCT others(38): Show |
C | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-54+25975_-54+2601 others(49): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274532 | ||||||
| chrX:102274532
|
CTTCCTCT others(41): Show |
C | 2 | a0001c0001t0001g0009a0001c0001t0001g0032 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-54+25975_-54+2602 others(52): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274532 | ||||||
| chrX:102274532
|
CTTCCTCT others(44): Show |
C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-54+25975_-54+2602 others(55): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274532 | ||||||
| chrX:102274534
|
TCCTCTTC others(9): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-54+25978_-54+2599 others(20): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274534 | |||||
| chrX:102274536
|
C | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(11): Show | 14 | HG01106.hp2 HG01952.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-54+25978C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274536 | ||||||
| chrX:102274538
|
CTTCCTCT others(29): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0001g0028 | 2 | HG02132.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-54+25981_-54+2601 others(40): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274538 | ||||||
| chrX:102274538
|
CTTCCTCT others(32): Show |
C | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-54+25981_-54+2601 others(43): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274538 | ||||||
| chrX:102274538
|
CTTCCTCT others(35): Show |
C | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0002t0001g0037 | 3 | HG01106.hp2 HG03516.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-54+25981_-54+2602 others(46): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274538 | ||||||
| chrX:102274538
|
CTTCCTCT others(38): Show |
C | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-54+25981_-54+2602 others(49): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274538 | ||||||
| chrX:102274541
|
C | CTT | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54+25983_-54+2598 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274541 | ||||||
| chrX:102274541
|
CCTCTTCT | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+25984_-54+2599 others(11): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274541 | ||||||
| chrX:102274542
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 6 | HG01952.hp1 HG02040.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+25984C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274542 | ||||||
| chrX:102274542
|
CTCTTCTT others(12): Show |
C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-54+25993_-54+2601 others(23): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274542 | |||||
| chrX:102274544
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54+25986C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274544 | ||||||
| chrX:102274544
|
CTTCTTCC others(17): Show |
C | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+25987_-54+2601 others(28): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274544 | ||||||
| chrX:102274544
|
CTTCTTCC others(32): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-54+25987_-54+2602 others(43): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274544 | ||||||
| chrX:102274545
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-54+25987T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274545 | ||||||
| chrX:102274546
|
TCTTC | T | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-54+25993_-54+2599 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274546 | |||||
| chrX:102274548
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-54+25990T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274548 | ||||||
| chrX:102274549
|
TC | T | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-54+25993delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274549 | |||||
| chrX:102274550
|
C | CCT | 1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-54+25993_-54+2599 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
C | CTT | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-54+25992_-54+2599 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274550 | ||||||
| chrX:102274550
|
CCTT | C | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-54+26077_-54+2607 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(2): Show |
C | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+26071_-54+2607 others(13): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(5): Show |
C | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-54+26068_-54+2607 others(16): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(29): Show |
C | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-54+26044_-54+2607 others(40): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(32): Show |
C | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-54+26041_-54+2607 others(43): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(35): Show |
C | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-54+26038_-54+2607 others(46): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(38): Show |
C | 1 | a0001c0001t0001g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-54+26035_-54+2607 others(49): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274550
|
CCTTCTTC others(44): Show |
C | 1 | a0001c0001t0001g0004 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-54+26029_-54+2607 others(55): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274550 | |||||
| chrX:102274551
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+25993C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274551 | ||||||
| chrX:102274551
|
CT | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+25995delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274551 | |||||
| chrX:102274551
|
CTTCT | C | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-54+25995_-54+2599 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274551 | |||||
| chrX:102274552
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0006 | 2 | HG02055.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+25994T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274552 | ||||||
| chrX:102274555
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-54+25997T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274555 | ||||||
| chrX:102274557
|
C | CTT | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26000_-54+2600 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274557 | |||||
| chrX:102274557
|
CTTCTTCT others(22): Show |
C | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-54+26000_-54+2602 others(33): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274557 | ||||||
| chrX:102274558
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(1): Show | 4 | HG03225.hp1 HG03942.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+26000T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274558 | ||||||
| chrX:102274560
|
CTTCT | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+26004_-54+2600 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274560 | |||||
| chrX:102274561
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG01952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-54+26003T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274561 | ||||||
| chrX:102274564
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0031 | 3 | HG03225.hp1 HG03942.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-54+26006T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274564 | ||||||
| chrX:102274566
|
CTT | C | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-54+26009_-54+2601 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274566 | ||||||
| chrX:102274567
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG01433.hp2 HG02886.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+26009T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274567 | ||||||
| chrX:102274567
|
T | TCTTCC | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26009_-54+2601 others(9): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274567 | ||||||
| chrX:102274568
|
T | TC | 1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-54+26011dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274568 | |||||
| chrX:102274569
|
CTT | C | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-54+26012_-54+2601 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274569 | ||||||
| chrX:102274570
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0031 | 2 | HG03225.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-54+26012T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274570 | ||||||
| chrX:102274572
|
CT | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+26016delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274572 | |||||
| chrX:102274572
|
CTT | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+26015_-54+2601 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274572 | ||||||
| chrX:102274573
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0021others(2): Show | 5 | HG01433.hp2 HG02083.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+26015T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274573 | ||||||
| chrX:102274575
|
CTT | C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-54+26018_-54+2601 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274575 | ||||||
| chrX:102274577
|
T | TC | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54+26020dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274577 | |||||
| chrX:102274578
|
CTT | C | 1 | a0001c0001t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-54+26021_-54+2602 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274578 | ||||||
| chrX:102274579
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG01433.hp2 HG02083.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+26021T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274579 | ||||||
| chrX:102274585
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0015 | 2 | HG02083.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-54+26027T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274585 | ||||||
| chrX:102274586
|
T | TC | 3 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01433.hp2 HG02886.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-54+26029dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274586 | |||||
| chrX:102274591
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-54+26033T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274591 | ||||||
| chrX:102274593
|
CTT | C | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-54+26036_-54+2603 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274593 | ||||||
| chrX:102274599
|
CT | C | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26043delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274599 | |||||
| chrX:102274599
|
CTT | C | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-54+26042_-54+2604 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274599 | ||||||
| chrX:102274635
|
CT | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+26080delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274635 | |||||
| chrX:102274685
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54+26127C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102274685 | ||||||
| chrX:102274813
|
T | TC | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26259dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274813 | |||||
| chrX:102274861
|
C | CT | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26306dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102274861 | |||||
| chrX:102275050
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+26494dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102275050 | |||||
| chrX:102276115
|
TCAGGTTT others(8): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+27558_-54+2757 others(19): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102276115 | ||||||
| chrX:102276152
|
T | TG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+27597dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276152 | |||||
| chrX:102276185
|
AT | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+27636delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276185 | |||||
| chrX:102276285
|
T | TA | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+27729dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276285 | |||||
| chrX:102276588
|
T | TC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28031dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276588 | |||||
| chrX:102276589
|
CT | C | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-54+28043delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276589 | |||||
| chrX:102276709
|
G | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-54+28151G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102276709 | ||||||
| chrX:102276759
|
T | TC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28203dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102276759 | |||||
| chrX:102277051
|
G | T | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+28493G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102277051 | ||||||
| chrX:102277127
|
A | AG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28570dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277127 | |||||
| chrX:102277213
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-54+28655G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102277213 | ||||||
| chrX:102277268
|
T | TG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28711dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277268 | |||||
| chrX:102277280
|
G | GT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28723dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277280 | |||||
| chrX:102277370
|
C | CT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+28815dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277370 | |||||
| chrX:102277677
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-54+29119A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102277677 | ||||||
| chrX:102277737
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-54+29179C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102277737 | ||||||
| chrX:102277966
|
T | TAC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-29059_-53-2905 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277966 | |||||
| chrX:102277985
|
A | AT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-29038dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102277985 | |||||
| chrX:102278005
|
T | TC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-29019dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278005 | |||||
| chrX:102278034
|
C | CT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28991dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278034 | |||||
| chrX:102278146
|
T | TG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28876dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278146 | |||||
| chrX:102278354
|
T | TC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28670dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278354 | |||||
| chrX:102278395
|
A | AT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28628dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278395 | |||||
| chrX:102278479
|
C | CT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28545dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278479 | |||||
| chrX:102278633
|
G | GT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28390dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278633 | |||||
| chrX:102278754
|
G | GT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-28268dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278754 | |||||
| chrX:102278811
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-53-28215G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102278811 | ||||||
| chrX:102278868
|
A | AT | 10 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-53-28141dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278868 | |||||
| chrX:102278868
|
AT | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0002t0003g0036 | 3 | HG00621.hp2 HG01358.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-53-28141delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102278868 | |||||
| chrX:102279054
|
T | TTG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-27972_-53-2797 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102279054 | ||||||
| chrX:102279055
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-27971G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102279055 | ||||||
| chrX:102279125
|
G | GT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-27899dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102279125 | |||||
| chrX:102279182
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 31 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-53-27844C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102279182 | ||||||
| chrX:102279218
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(9): Show | 12 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-53-27808T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102279218 | ||||||
| chrX:102279358
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-27668A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102279358 | ||||||
| chrX:102280630
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0010 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-26396C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102280630 | ||||||
| chrX:102280793
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-53-26233C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102280793 | ||||||
| chrX:102281220
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-53-25806G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102281220 | ||||||
| chrX:102281728
|
A | AC | 4 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-25289dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102281728 | |||||
| chrX:102281728
|
AC | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-53-25289delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102281728 | |||||
| chrX:102281970
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0010 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-25056G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102281970 | ||||||
| chrX:102281975
|
AT | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(28): Show | 31 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-53-25035delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102281975 | |||||
| chrX:102281975
|
ATT | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0032others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53-25036_-53-2503 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102281975 | |||||
| chrX:102282053
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-53-24973C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282053 | ||||||
| chrX:102282113
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-24913C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282113 | ||||||
| chrX:102282242
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-53-24784C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282242 | ||||||
| chrX:102282301
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-53-24725G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282301 | ||||||
| chrX:102282403
|
CT | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0002g0005 | 3 | HG03942.hp1 HG04199.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-53-24622delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282403 | ||||||
| chrX:102282433
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-24593C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282433 | ||||||
| chrX:102282522
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-53-24504A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282522 | ||||||
| chrX:102282923
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-53-24103A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102282923 | ||||||
| chrX:102283856
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-53-23170T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102283856 | ||||||
| chrX:102284212
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-22814T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102284212 | ||||||
| chrX:102284723
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-53-22303G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102284723 | ||||||
| chrX:102285185
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-21841A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102285185 | ||||||
| chrX:102285472
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-53-21554C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102285472 | ||||||
| chrX:102285623
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-21403T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102285623 | ||||||
| chrX:102285918
|
G | GT | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-21100dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102285918 | |||||
| chrX:102285939
|
TTG | T | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-21085_-53-2108 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102285939 | |||||
| chrX:102285941
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-21085G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102285941 | ||||||
| chrX:102285941
|
GT | G | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-53-21070delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102285941 | |||||
| chrX:102285941
|
GTT | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(22): Show | 25 | HG00280.hp2 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-53-21071_-53-2107 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102285941 | |||||
| chrX:102285941
|
GTTT | G | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-21072_-53-2107 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102285941 | |||||
| chrX:102285948
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-21078T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102285948 | ||||||
| chrX:102286013
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-53-21013C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286013 | ||||||
| chrX:102286093
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-20933T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286093 | ||||||
| chrX:102286167
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-53-20859G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286167 | ||||||
| chrX:102286286
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0028 | 3 | HG02129.hp2 HG02132.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-20740C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286286 | ||||||
| chrX:102286295
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0014 | 2 | HG02300.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-53-20731C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286295 | ||||||
| chrX:102286298
|
G | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0037 | 2 | HG02886.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-53-20728G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286298 | ||||||
| chrX:102286735
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0002g0005 | 3 | HG03942.hp1 HG04199.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-53-20291C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286735 | ||||||
| chrX:102286924
|
T | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0008 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-20102T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102286924 | ||||||
| chrX:102287330
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.-53-19696G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102287330 | ||||||
| chrX:102287885
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-53-19141T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102287885 | ||||||
| chrX:102288375
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-18651A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102288375 | ||||||
| chrX:102288711
|
G | T | 2 | a0001c0002t0001g0038a0001c0002t0003g0036 | 2 | HG00140.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-53-18315G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102288711 | ||||||
| chrX:102288944
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-18082C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102288944 | ||||||
| chrX:102288993
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-18033T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102288993 | ||||||
| chrX:102288996
|
C | CT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-18011dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102288996 | |||||
| chrX:102288996
|
C | CTTT | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-18013_-53-1801 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102288996 | |||||
| chrX:102288996
|
CT | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-53-18011delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102288996 | |||||
| chrX:102288996
|
CTT | C | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-53-18012_-53-1801 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102288996 | |||||
| chrX:102289002
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-18024T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289002 | ||||||
| chrX:102289004
|
T | TC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-53-18022_-53-1802 others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289004 | ||||||
| chrX:102289222
|
A | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-53-17804A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289222 | ||||||
| chrX:102289223
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-53-17803T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289223 | ||||||
| chrX:102289496
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0030others(3): Show | 6 | HG00140.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-17530G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289496 | ||||||
| chrX:102289667
|
C | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53-17359C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289667 | ||||||
| chrX:102289668
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53-17358C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289668 | ||||||
| chrX:102289669
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53-17357A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289669 | ||||||
| chrX:102289714
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0030others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-17312G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289714 | ||||||
| chrX:102289795
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53-17231A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102289795 | ||||||
| chrX:102290020
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-17006C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290020 | ||||||
| chrX:102290064
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-53-16962G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290064 | ||||||
| chrX:102290067
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-16959T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290067 | ||||||
| chrX:102290184
|
C | T | 4 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0038others(1): Show | 4 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-16842C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290184 | ||||||
| chrX:102290234
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-16792T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290234 | ||||||
| chrX:102290265
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-16761T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290265 | ||||||
| chrX:102290492
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-53-16534T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102290492 | ||||||
| chrX:102290608
|
C | CA | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-16412dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102290608 | |||||
| chrX:102290712
|
T | TG | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-16308dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102290712 | |||||
| chrX:102291255
|
AT | A | 1 | a0001c0001t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-53-15768delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102291255 | |||||
| chrX:102291310
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-15716C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102291310 | ||||||
| chrX:102291553
|
C | CT | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-15460dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102291553 | |||||
| chrX:102291696
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-15330C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102291696 | ||||||
| chrX:102291963
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-53-15063T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102291963 | ||||||
| chrX:102292344
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-14682A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102292344 | ||||||
| chrX:102292465
|
A | AGAT | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-53-14560_-53-1455 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102292465 | |||||
| chrX:102292953
|
G | GT | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(9): Show | 12 | HG00738.hp1 HG01106.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-53-14059dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102292953 | |||||
| chrX:102292953
|
GT | G | 3 | a0001c0001t0001g0015a0001c0002t0001g0034a0001c0002t0001g0037 | 3 | HG02258.hp1 HG03098.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-53-14059delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102292953 | |||||
| chrX:102293324
|
T | G | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-53-13702T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293324 | ||||||
| chrX:102293338
|
TTG | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-13686_-53-1368 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293338 | |||||
| chrX:102293523
|
C | CCA | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-53-13502_-53-1350 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293523 | |||||
| chrX:102293524
|
C | CAT | 4 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0027others(1): Show | 4 | HG00140.hp1 HG01106.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-13461_-53-1346 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
C | CATAT | 2 | a0001c0001t0001g0009a0001c0001t0001g0032 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-53-13463_-53-1346 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
C | CATATAT | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-13465_-53-1346 others(10): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
C | CATATATA others(1): Show |
1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-13467_-53-1346 others(12): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CAT | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0002t0001g0037 | 3 | HG00621.hp2 HG03225.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-53-13461_-53-1346 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATAT | C | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-13463_-53-1346 others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATATAT | C | 1 | a0001c0001t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-13465_-53-1346 others(10): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATATATA others(1): Show |
C | 5 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(2): Show | 5 | HG02071.hp1 HG02258.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-13467_-53-1346 others(12): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATATATA others(3): Show |
C | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-13469_-53-1346 others(14): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-13471_-53-1346 others(16): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293524
|
CATATATA others(19): Show |
C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-53-13485_-53-1346 others(30): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293524 | |||||
| chrX:102293528
|
TATATATA | T | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-53-13497_-53-1349 others(11): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293528 | ||||||
| chrX:102293557
|
ATATATAT others(2): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-53-13467_-53-1345 others(13): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293557 | |||||
| chrX:102293565
|
A | ATG | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-53-13460_-53-1345 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293565 | |||||
| chrX:102293565
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-53-13461A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293565 | ||||||
| chrX:102293565
|
ATTT | A | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-53-13460_-53-1345 others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293565 | ||||||
| chrX:102293579
|
GT | G | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-53-13434delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102293579 | |||||
| chrX:102293588
|
T | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(14): Show | 17 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-53-13438T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293588 | ||||||
| chrX:102293821
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-53-13205G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102293821 | ||||||
| chrX:102294045
|
T | TG | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53-12975dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102294045 | |||||
| chrX:102294050
|
G | GA | 2 | a0001c0001t0001g0003a0001c0001t0002g0005 | 2 | HG02129.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-53-12976_-53-1297 others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294050 | ||||||
| chrX:102294051
|
G | GA | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-53-12974dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102294051 | |||||
| chrX:102294085
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-53-12941A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294085 | ||||||
| chrX:102294165
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-12861A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294165 | ||||||
| chrX:102294186
|
A | T | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-12840A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294186 | ||||||
| chrX:102294188
|
TA | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(3): Show | 6 | HG02055.hp2 HG02129.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-12823delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102294188 | |||||
| chrX:102294255
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-53-12771A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294255 | ||||||
| chrX:102294457
|
G | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(13): Show | 16 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53-12569G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294457 | ||||||
| chrX:102294624
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(22): Show | 25 | HG00140.hp1 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-53-12402C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102294624 | ||||||
| chrX:102295222
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53-11804G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102295222 | ||||||
| chrX:102295555
|
G | GC | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-53-11462dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102295555 | |||||
| chrX:102295555
|
G | GCC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-11463_-53-1146 others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102295555 | |||||
| chrX:102296005
|
G | GC | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-53-11016dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102296005 | |||||
| chrX:102296048
|
C | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-53-10978C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102296048 | ||||||
| chrX:102296595
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-10431T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102296595 | ||||||
| chrX:102296657
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-10369C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102296657 | ||||||
| chrX:102297436
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0008 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-9590C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102297436 | ||||||
| chrX:102297467
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-53-9559T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102297467 | ||||||
| chrX:102297473
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-53-9553T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102297473 | ||||||
| chrX:102297516
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-9510C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102297516 | ||||||
| chrX:102298019
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(6): Show | 9 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-9007C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102298019 | ||||||
| chrX:102298192
|
T | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-53-8834T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102298192 | ||||||
| chrX:102298463
|
C | CA | 7 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0025others(4): Show | 7 | HG00621.hp2 HG01433.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-8540dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298463 | |||||
| chrX:102298463
|
C | CAA | 3 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0002g0005 | 3 | HG02071.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-53-8541_-53-8540d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298463 | |||||
| chrX:102298463
|
C | CAAA | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG01952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-53-8542_-53-8540d others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298463 | |||||
| chrX:102298463
|
CA | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-8540delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298463 | |||||
| chrX:102298463
|
CAA | C | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-8541_-53-8540d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298463 | |||||
| chrX:102298700
|
TC | T | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-8323delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102298700 | |||||
| chrX:102299023
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-8003T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102299023 | ||||||
| chrX:102299336
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-53-7690C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102299336 | ||||||
| chrX:102299477
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-7549C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102299477 | ||||||
| chrX:102299781
|
AT | A | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-7241delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102299781 | |||||
| chrX:102300170
|
A | T | 3 | a0001c0002t0001g0034a0001c0002t0001g0038a0001c0002t0003g0036 | 3 | HG00140.hp1 HG01358.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-53-6856A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102300170 | ||||||
| chrX:102300184
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53-6842G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102300184 | ||||||
| chrX:102300881
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-53-6145C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102300881 | ||||||
| chrX:102301020
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-53-6006T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102301020 | ||||||
| chrX:102301136
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-53-5890C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102301136 | ||||||
| chrX:102301339
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-5687T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102301339 | ||||||
| chrX:102301354
|
TA | T | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-5669delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102301354 | |||||
| chrX:102301456
|
G | GA | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-5569dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102301456 | |||||
| chrX:102301577
|
AG | A | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-5447delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102301577 | |||||
| chrX:102301697
|
TA | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-5324delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102301697 | |||||
| chrX:102301715
|
GCTGA | G | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-53-5308_-53-5305d others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102301715 | |||||
| chrX:102302166
|
CT | C | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-4853delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102302166 | |||||
| chrX:102302420
|
A | C | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-4606A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102302420 | ||||||
| chrX:102302702
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-4324C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102302702 | ||||||
| chrX:102302788
|
TA | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0028others(2): Show | 5 | HG00280.hp2 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-4225delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102302788 | |||||
| chrX:102302788
|
TAA | T | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-53-4226_-53-4225d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102302788 | |||||
| chrX:102302864
|
C | G | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-53-4162C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102302864 | ||||||
| chrX:102303449
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-3577A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102303449 | ||||||
| chrX:102303710
|
T | TTG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-3314_-53-3313d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102303710 | |||||
| chrX:102303790
|
GA | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-3233delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102303790 | |||||
| chrX:102303969
|
A | AG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-3056dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102303969 | |||||
| chrX:102304032
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-2992delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304032 | |||||
| chrX:102304068
|
C | CG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-2953dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304068 | |||||
| chrX:102304068
|
CG | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0028 | 2 | HG02132.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-53-2953delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304068 | |||||
| chrX:102304148
|
AG | A | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-2876delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304148 | |||||
| chrX:102304283
|
A | AT | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-2739dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304283 | |||||
| chrX:102304294
|
CA | C | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-2729delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304294 | |||||
| chrX:102304500
|
T | TG | 1 | a0001c0001t0001g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-53-2520dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304500 | |||||
| chrX:102304543
|
TG | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-2480delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304543 | |||||
| chrX:102304660
|
C | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0027others(2): Show | 5 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-2366C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102304660 | ||||||
| chrX:102304669
|
T | TC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-2354dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304669 | |||||
| chrX:102304726
|
G | GC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-2299dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304726 | |||||
| chrX:102304774
|
C | CA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-2248dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304774 | |||||
| chrX:102304787
|
C | CA | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0023others(1): Show | 4 | HG02040.hp1 HG04199.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-2216dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304787 | |||||
| chrX:102304787
|
C | CAA | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-2217_-53-2216d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304787 | |||||
| chrX:102304787
|
CA | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0029others(4): Show | 7 | HG01099.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53-2216delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304787 | |||||
| chrX:102304787
|
CAA | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(6): Show | 9 | HG00280.hp2 HG00621.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-2217_-53-2216d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304787 | |||||
| chrX:102304787
|
CAAA | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0028 | 3 | HG02055.hp2 HG02132.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-2218_-53-2216d others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102304787 | |||||
| chrX:102305102
|
C | CA | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53-1924_-53-1923i others(3): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305102 | ||||||
| chrX:102305375
|
T | TC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1647dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305375 | |||||
| chrX:102305393
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(15): Show | 18 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.-53-1633T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305393 | ||||||
| chrX:102305524
|
AC | A | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1500delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305524 | |||||
| chrX:102305732
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1293dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305732 | |||||
| chrX:102305737
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1287dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305737 | |||||
| chrX:102305745
|
C | CG | 3 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG01952.hp1 HG02071.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-53-1279dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305745 | |||||
| chrX:102305817
|
GGGGGT | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-53-1190_-53-1186d others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305817 | |||||
| chrX:102305822
|
T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-1200dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305822 | |||||
| chrX:102305822
|
TG | T | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-1200delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305822 | |||||
| chrX:102305832
|
T | TG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1190dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305832 | |||||
| chrX:102305837
|
T | TG | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-53-1186dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305837 | |||||
| chrX:102305841
|
T | TG | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(3): Show | 6 | HG01358.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-1179dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305841 | |||||
| chrX:102305849
|
G | GC | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-53-1175dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305849 | |||||
| chrX:102305851
|
C | CG | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53-1170dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305851 | |||||
| chrX:102305855
|
G | GT | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-53-1171_-53-1170i others(3): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305855 | ||||||
| chrX:102305859
|
CG | C | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53-1164delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305859 | |||||
| chrX:102305863
|
AG | A | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-1160delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305863 | |||||
| chrX:102305866
|
G | GGT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1160_-53-1159i others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305866 | ||||||
| chrX:102305867
|
T | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1159T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305867 | ||||||
| chrX:102305867
|
T | TG | 3 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022 | 3 | HG00642.hp2 HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-1153dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305867 | |||||
| chrX:102305885
|
C | CG | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-1138dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305885 | |||||
| chrX:102305885
|
C | CGGGAGGG others(11): Show |
1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-53-1126_-53-1125i others(20): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305885 | |||||
| chrX:102305885
|
CGGGAGGG others(10): Show |
C | 4 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-1126_-53-1110d others(19): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305885 | |||||
| chrX:102305891
|
G | GCGT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1135_-53-1134i others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305891 | ||||||
| chrX:102305893
|
T | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1133T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102305893 | ||||||
| chrX:102305893
|
T | TG | 11 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG00140.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-53-1126dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305893 | |||||
| chrX:102305896
|
G | GGGGGT | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53-1125_-53-1121d others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305896 | |||||
| chrX:102305906
|
A | AG | 1 | a0001c0001t0001g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-53-1117dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305906 | |||||
| chrX:102305910
|
T | TG | 4 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0002g0005others(1): Show | 4 | HG00621.hp2 HG02886.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-1110dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305910 | |||||
| chrX:102305937
|
T | TG | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-1083dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305937 | |||||
| chrX:102305946
|
T | TG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-1077dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305946 | |||||
| chrX:102305962
|
A | AG | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-53-1062dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102305962 | |||||
| chrX:102306004
|
G | GA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-1019dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306004 | |||||
| chrX:102306015
|
T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-53-1010dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306015 | |||||
| chrX:102306021
|
C | CGT | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53-993_-53-992dup others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306021 | |||||
| chrX:102306023
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-53-1003T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102306023 | ||||||
| chrX:102306156
|
T | TG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-866dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306156 | |||||
| chrX:102306225
|
T | TC | 2 | a0001c0001t0001g0017a0001c0001t0002g0005 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-53-793dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306225 | |||||
| chrX:102306235
|
T | TC | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-788dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306235 | |||||
| chrX:102306239
|
G | GC | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-53-782dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306239 | |||||
| chrX:102306265
|
GC | G | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-759delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306265 | |||||
| chrX:102306277
|
GC | G | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-746delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306277 | |||||
| chrX:102306315
|
G | GC | 2 | a0001c0001t0001g0029a0001c0001t0002g0005 | 2 | HG01433.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-53-707dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306315 | |||||
| chrX:102306364
|
TC | T | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-659delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306364 | |||||
| chrX:102306519
|
AT | A | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-53-500delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306519 | |||||
| chrX:102306526
|
TA | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-53-495delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306526 | |||||
| chrX:102306621
|
CT | C | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-402delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306621 | |||||
| chrX:102306651
|
A | AT | 1 | a0001c0001t0001g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-53-367dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306651 | |||||
| chrX:102306658
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-368T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102306658 | ||||||
| chrX:102306758
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-53-268T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | chrX | 102306758 | ||||||
| chrX:102306771
|
G | GATTCC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-254_-53-250dup others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306771 | |||||
| chrX:102306776
|
CT | C | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-247delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306776 | |||||
| chrX:102306801
|
TC | T | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-223delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306801 | |||||
| chrX:102306877
|
T | TA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-148dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306877 | |||||
| chrX:102306889
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-135dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102306889 | |||||
| chrX:102307002
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-22delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chrX | 102307002 | |||||
| chrX:102307140
|
AT | A | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.43+26delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307140 | |||||
| chrX:102307157
|
G | GC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+37dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307157 | |||||
| chrX:102307208
|
TG | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+90delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307208 | |||||
| chrX:102307220
|
AT | A | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+106delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307220 | |||||
| chrX:102307242
|
A | AG | 2 | a0001c0001t0001g0007a0001c0001t0002g0005 | 2 | HG02145.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.43+123dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307242 | |||||
| chrX:102307276
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+158dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307276 | |||||
| chrX:102307276
|
AC | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+158delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307276 | |||||
| chrX:102307294
|
CT | C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+175delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307294 | |||||
| chrX:102307335
|
C | CA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+216dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307335 | |||||
| chrX:102307353
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+234delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307353 | |||||
| chrX:102307385
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+264A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307385 | ||||||
| chrX:102307392
|
GT | G | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+273delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307392 | |||||
| chrX:102307407
|
AT | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+290delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307407 | |||||
| chrX:102307428
|
CA | C | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+308delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307428 | ||||||
| chrX:102307432
|
CT | C | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+312delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307432 | ||||||
| chrX:102307559
|
C | CA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+441dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307559 | |||||
| chrX:102307569
|
GC | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+453delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307569 | |||||
| chrX:102307590
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+469A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307590 | ||||||
| chrX:102307642
|
T | TA | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.43+527dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307642 | |||||
| chrX:102307642
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+527delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307642 | |||||
| chrX:102307662
|
GA | G | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+543delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307662 | |||||
| chrX:102307709
|
C | CA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+588_43+589insA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307709 | ||||||
| chrX:102307731
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.43+610T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102307731 | ||||||
| chrX:102307810
|
T | TG | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+690dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307810 | |||||
| chrX:102307926
|
CG | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0013 | 2 | HG02145.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.43+808delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307926 | |||||
| chrX:102307939
|
G | GT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+820dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307939 | |||||
| chrX:102307962
|
TG | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+843delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102307962 | |||||
| chrX:102308006
|
GA | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+888delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308006 | |||||
| chrX:102308013
|
GT | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+894delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308013 | |||||
| chrX:102308015
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(1): Show | 4 | HG03471.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+894T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308015 | ||||||
| chrX:102308041
|
G | GC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+922dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308041 | |||||
| chrX:102308048
|
A | AG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+930dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308048 | |||||
| chrX:102308140
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1019C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308140 | ||||||
| chrX:102308141
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1020G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308141 | ||||||
| chrX:102308170
|
G | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1049G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308170 | ||||||
| chrX:102308176
|
T | TC | 2 | a0001c0001t0001g0003a0001c0001t0001g0029 | 2 | HG01433.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.43+1057dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308176 | |||||
| chrX:102308224
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1103_43+1104ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308224 | ||||||
| chrX:102308338
|
CA | C | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+1220delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308338 | |||||
| chrX:102308370
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.43+1249C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308370 | ||||||
| chrX:102308527
|
A | AG | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+1409dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308527 | |||||
| chrX:102308538
|
TG | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1419delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308538 | |||||
| chrX:102308600
|
C | CT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+1483dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308600 | |||||
| chrX:102308668
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1554delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308668 | |||||
| chrX:102308692
|
GA | G | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1574delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308692 | |||||
| chrX:102308704
|
AC | A | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43+1585delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308704 | |||||
| chrX:102308759
|
A | AG | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1638_43+1639ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308759 | ||||||
| chrX:102308766
|
T | TA | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1649dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308766 | |||||
| chrX:102308786
|
G | GC | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1666dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308786 | |||||
| chrX:102308791
|
G | GA | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+1674dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308791 | |||||
| chrX:102308802
|
A | AG | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43+1683dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308802 | |||||
| chrX:102308829
|
A | AT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1709dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308829 | |||||
| chrX:102308907
|
AT | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1789delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308907 | |||||
| chrX:102308920
|
A | T | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1799A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308920 | ||||||
| chrX:102308963
|
AG | A | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1844delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308963 | |||||
| chrX:102308975
|
C | A | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1854C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102308975 | ||||||
| chrX:102308980
|
GT | G | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+1862delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308980 | |||||
| chrX:102308987
|
CA | C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1868delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308987 | |||||
| chrX:102308993
|
AT | A | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.43+1874delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102308993 | |||||
| chrX:102309001
|
CA | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43+1882delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309001 | |||||
| chrX:102309057
|
CA | C | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+1939delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309057 | |||||
| chrX:102309075
|
TA | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+1956delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309075 | |||||
| chrX:102309089
|
AC | A | 1 | a0001c0001t0001g0028 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.43+1971delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309089 | |||||
| chrX:102309101
|
G | GT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+1981dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309101 | |||||
| chrX:102309126
|
A | AG | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2007dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309126 | |||||
| chrX:102309139
|
TC | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2021delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309139 | |||||
| chrX:102309229
|
T | TAC | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+2109_43+2110dup others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309229 | |||||
| chrX:102309247
|
T | TA | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+2136dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309247 | |||||
| chrX:102309247
|
T | TAAAA | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2133_43+2136dup others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309247 | |||||
| chrX:102309247
|
TA | T | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2136delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309247 | |||||
| chrX:102309266
|
T | TG | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+2145_43+2146ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309266 | ||||||
| chrX:102309319
|
C | CGGTA | 1 | a0001c0001t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.43+2199_43+2202dup others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309319 | |||||
| chrX:102309354
|
T | TG | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2236dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309354 | |||||
| chrX:102309354
|
TG | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2236delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309354 | |||||
| chrX:102309372
|
AC | A | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2255delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309372 | |||||
| chrX:102309408
|
G | GA | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43+2289dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309408 | |||||
| chrX:102309418
|
C | CCTTACAA | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+2298_43+2304dup others(7): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309418 | |||||
| chrX:102309429
|
GA | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2312delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309429 | |||||
| chrX:102309482
|
T | TC | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+2362dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309482 | |||||
| chrX:102309537
|
CA | C | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+2417delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309537 | ||||||
| chrX:102309567
|
TA | T | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43+2450delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309567 | |||||
| chrX:102309574
|
G | GA | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+2458dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309574 | |||||
| chrX:102309611
|
CA | C | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2492delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309611 | |||||
| chrX:102309625
|
G | GA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+2508dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309625 | |||||
| chrX:102309631
|
TA | T | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+2515delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309631 | |||||
| chrX:102309686
|
AC | A | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+2567delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309686 | |||||
| chrX:102309706
|
AC | A | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2587delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309706 | |||||
| chrX:102309852
|
GA | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0012 | 2 | HG02145.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.43+2734delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309852 | |||||
| chrX:102309855
|
AG | A | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+2736delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309855 | |||||
| chrX:102309861
|
CA | C | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2741delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309861 | ||||||
| chrX:102309903
|
T | TC | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+2782_43+2783ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309903 | ||||||
| chrX:102309906
|
TCTCTCTC others(5): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2797_43+2808del others(12): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309906 | |||||
| chrX:102309914
|
T | TC | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2794dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309914 | |||||
| chrX:102309918
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+2797G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309918 | ||||||
| chrX:102309920
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+2799T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309920 | ||||||
| chrX:102309928
|
TCTCACAC others(1): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.43+2809_43+2816del others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309928 | |||||
| chrX:102309930
|
TCA | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(3): Show | 6 | HG00642.hp2 HG01099.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+2844_43+2845del others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309930 | |||||
| chrX:102309930
|
TCACA | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(5): Show | 8 | HG00621.hp2 HG01433.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+2842_43+2845del others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309930 | |||||
| chrX:102309930
|
TCACACA | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(11): Show | 14 | HG00738.hp1 HG01106.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.43+2840_43+2845del others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309930 | |||||
| chrX:102309930
|
TCACACAC others(1): Show |
T | 3 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0013 | 3 | HG00280.hp2 NA18747.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.43+2838_43+2845del others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102309930 | |||||
| chrX:102309932
|
A | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2811A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309932 | ||||||
| chrX:102309934
|
A | T | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+2813A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309934 | ||||||
| chrX:102309936
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+2815A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309936 | ||||||
| chrX:102309938
|
A | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2817A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309938 | ||||||
| chrX:102309944
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43+2823A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309944 | ||||||
| chrX:102309951
|
CACACA | C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2831_43+2835del others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309951 | ||||||
| chrX:102309957
|
CA | C | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2837delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102309957 | ||||||
| chrX:102310012
|
A | AG | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+2894dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310012 | |||||
| chrX:102310023
|
TG | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2905delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310023 | |||||
| chrX:102310057
|
A | AT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2937dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310057 | |||||
| chrX:102310062
|
A | AC | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+2942dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310062 | |||||
| chrX:102310069
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.43+2948A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310069 | ||||||
| chrX:102310081
|
TA | T | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+2962delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310081 | |||||
| chrX:102310099
|
T | TG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+2982dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310099 | |||||
| chrX:102310113
|
T | C | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+2992T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310113 | ||||||
| chrX:102310133
|
G | GT | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+3016dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310133 | |||||
| chrX:102310140
|
T | TG | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+3020dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310140 | |||||
| chrX:102310171
|
A | AG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3051dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310171 | |||||
| chrX:102310201
|
A | AG | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+3082dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310201 | |||||
| chrX:102310203
|
G | GC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+3083dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310203 | |||||
| chrX:102310214
|
AT | A | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+3096delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310214 | |||||
| chrX:102310221
|
C | CA | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+3100_43+3101ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310221 | ||||||
| chrX:102310229
|
G | GT | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+3110dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310229 | |||||
| chrX:102310231
|
TC | T | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+3112delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310231 | |||||
| chrX:102310255
|
TG | T | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+3136delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310255 | |||||
| chrX:102310278
|
C | CT | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+3161dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310278 | |||||
| chrX:102310298
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3177T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310298 | ||||||
| chrX:102310299
|
T | A | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3178T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310299 | ||||||
| chrX:102310300
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3179T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310300 | ||||||
| chrX:102310301
|
T | G | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3180T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310301 | ||||||
| chrX:102310302
|
T | A | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3181T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310302 | ||||||
| chrX:102310303
|
G | C | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3182G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310303 | ||||||
| chrX:102310304
|
T | A | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3183T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310304 | ||||||
| chrX:102310305
|
A | C | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3184A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310305 | ||||||
| chrX:102310306
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3185A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310306 | ||||||
| chrX:102310307
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3186G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310307 | ||||||
| chrX:102310309
|
T | G | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3188T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310309 | ||||||
| chrX:102310313
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3194delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310313 | |||||
| chrX:102310314
|
A | T | 1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+3193A>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310314 | ||||||
| chrX:102310404
|
T | TG | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+3285dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310404 | |||||
| chrX:102310410
|
CA | C | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.43+3293delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310410 | |||||
| chrX:102310426
|
CA | C | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+3309delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310426 | |||||
| chrX:102310453
|
TG | T | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+3336delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310453 | |||||
| chrX:102310540
|
C | A | 1 | a0001c0001t0004g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+3419C>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310540 | ||||||
| chrX:102310579
|
C | CA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3459dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310579 | |||||
| chrX:102310592
|
G | GA | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+3472dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310592 | |||||
| chrX:102310622
|
AG | A | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+3503delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310622 | |||||
| chrX:102310638
|
G | GT | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+3521dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310638 | |||||
| chrX:102310650
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3529_43+3530ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310650 | ||||||
| chrX:102310668
|
A | AC | 1 | a0001c0001t0001g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+3548dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310668 | |||||
| chrX:102310708
|
C | CG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3589dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310708 | |||||
| chrX:102310708
|
CG | C | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+3589delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310708 | |||||
| chrX:102310724
|
G | GT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3607dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310724 | |||||
| chrX:102310741
|
GT | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3621delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310741 | ||||||
| chrX:102310791
|
G | GT | 1 | a0001c0001t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43+3670_43+3671ins others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102310791 | ||||||
| chrX:102310910
|
GT | G | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+3791delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310910 | |||||
| chrX:102310919
|
GA | G | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+3802delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102310919 | |||||
| chrX:102311041
|
TA | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+3923delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311041 | |||||
| chrX:102311143
|
AC | A | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+4025delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311143 | |||||
| chrX:102311193
|
TG | T | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+4074delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311193 | |||||
| chrX:102311250
|
TC | T | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.43+4133delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311250 | |||||
| chrX:102311475
|
GC | G | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+4356delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311475 | |||||
| chrX:102311565
|
CG | C | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43+4446delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311565 | |||||
| chrX:102311566
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+4445G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102311566 | ||||||
| chrX:102311791
|
T | TA | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43+4673dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311791 | |||||
| chrX:102311858
|
AC | A | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43+4740delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311858 | |||||
| chrX:102311873
|
T | TA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+4755dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311873 | |||||
| chrX:102311908
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.43+4787T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102311908 | ||||||
| chrX:102311971
|
T | TC | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43+4853dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102311971 | |||||
| chrX:102312031
|
T | TA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+4911dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312031 | |||||
| chrX:102312065
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.44-4894dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312065 | |||||
| chrX:102312142
|
C | CT | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.44-4820dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312142 | |||||
| chrX:102312157
|
GA | G | 1 | a0001c0002t0003g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.44-4803delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312157 | |||||
| chrX:102312181
|
AT | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.44-4771delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312181 | |||||
| chrX:102312181
|
ATT | A | 3 | a0001c0001t0002g0005a0001c0002t0001g0035a0001c0002t0001g0037 | 3 | HG02886.hp2 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.44-4772_44-4771del others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312181 | |||||
| chrX:102312292
|
T | TG | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.44-4670dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312292 | |||||
| chrX:102312305
|
C | T | 2 | a0001c0002t0001g0035a0001c0002t0001g0037 | 2 | HG02886.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.44-4658C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102312305 | ||||||
| chrX:102312339
|
G | GC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-4622dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312339 | |||||
| chrX:102312533
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.44-4430C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102312533 | ||||||
| chrX:102312631
|
A | AG | 2 | a0001c0001t0001g0015a0001c0001t0001g0029 | 2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.44-4327dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312631 | |||||
| chrX:102312683
|
C | CT | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-4278dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312683 | |||||
| chrX:102312699
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.44-4264T>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102312699 | ||||||
| chrX:102312712
|
G | GA | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.44-4248dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312712 | |||||
| chrX:102312744
|
GC | G | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-4216delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312744 | |||||
| chrX:102312839
|
T | TC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-4123dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312839 | |||||
| chrX:102312969
|
T | TA | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-3992dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102312969 | |||||
| chrX:102313020
|
A | AG | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-3939dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313020 | |||||
| chrX:102313097
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-3863dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313097 | |||||
| chrX:102313114
|
C | G | 2 | a0001c0002t0001g0038a0001c0002t0003g0036 | 2 | HG00140.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.44-3849C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102313114 | ||||||
| chrX:102313138
|
T | TC | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-3824dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313138 | |||||
| chrX:102313239
|
TG | T | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-3722delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313239 | |||||
| chrX:102313245
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0026 | 3 | HG03471.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.44-3718C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102313245 | ||||||
| chrX:102313379
|
T | TG | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-3582dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313379 | |||||
| chrX:102313582
|
A | AC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-3377dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313582 | |||||
| chrX:102313669
|
AT | A | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.44-3290delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313669 | |||||
| chrX:102313716
|
G | GA | 1 | a0001c0002t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.44-3240dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313716 | |||||
| chrX:102313792
|
AATGT | A | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-3170_44-3167del others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102313792 | ||||||
| chrX:102313929
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-3032dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313929 | |||||
| chrX:102313983
|
A | AG | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-2978dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313983 | |||||
| chrX:102313996
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-2966dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102313996 | |||||
| chrX:102314307
|
CG | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-2654delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314307 | |||||
| chrX:102314633
|
T | TC | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-2329dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314633 | |||||
| chrX:102314674
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44-2289C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102314674 | ||||||
| chrX:102314693
|
T | TTC | 1 | a0001c0002t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-2268_44-2267dup others(2): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314693 | |||||
| chrX:102314736
|
AC | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-2224delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314736 | |||||
| chrX:102314858
|
AG | A | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-2102delG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314858 | |||||
| chrX:102314951
|
TC | T | 1 | a0001c0001t0001g0003 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-2010delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102314951 | |||||
| chrX:102315138
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.44-1825T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102315138 | ||||||
| chrX:102315146
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44-1817A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102315146 | ||||||
| chrX:102315173
|
A | AG | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-1789dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315173 | |||||
| chrX:102315249
|
C | CA | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-1713dupA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315249 | |||||
| chrX:102315314
|
C | CT | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-1645dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315314 | |||||
| chrX:102315465
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.44-1498T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | chrX | 102315465 | ||||||
| chrX:102315469
|
GA | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-1490delA | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315469 | |||||
| chrX:102315511
|
A | AG | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-1448dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315511 | |||||
| chrX:102315900
|
A | AG | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-1060dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315900 | |||||
| chrX:102315921
|
T | TC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-1041dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102315921 | |||||
| chrX:102316175
|
T | TG | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-786dupG | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102316175 | |||||
| chrX:102316356
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-606dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chrX | 102316356 | |||||
| chrX:102317285
|
G | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.234-94G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 4/22 | chrX | 102317285 | ||||||
| chrX:102317297
|
G | GC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234-79dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chrX | 102317297 | |||||
| chrX:102317698
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.385-135T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 5/22 | chrX | 102317698 | ||||||
| chrX:102318002
|
G | GT | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.469-24dupT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chrX | 102318002 | |||||
| chrX:102318019
|
TC | T | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.469-6delC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chrX | 102318019 | |||||
| chrX:102318150
|
G | GC | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.573+21dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chrX | 102318150 | |||||
| chrX:102318172
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.573+40A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 7/22 | chrX | 102318172 | ||||||
| chrX:102318405
|
T | TCAC | 2 | a0001c0001t0001g0008a0001c0001t0001g0015 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.655-68_655-66dupCC others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chrX | 102318405 | |||||
| chrX:102318405
|
TCAC | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-68_655-66delCC others(1): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chrX | 102318405 | |||||
| chrX:102318405
|
TCACCAC | T | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.655-71_655-66delCC others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chrX | 102318405 | |||||
| chrX:102319377
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1031+31G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 12/22 | chrX | 102319377 | ||||||
| chrX:102319476
|
A | ACT | 16 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(13): Show | 16 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1031+154_1031+155d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chrX | 102319476 | |||||
| chrX:102319823
|
T | TC | 1 | a0001c0001t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1031+483dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chrX | 102319823 | |||||
| chrX:102320004
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(7): Show | 10 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1031+658A>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 12/22 | chrX | 102320004 | ||||||
| chrX:102320553
|
CT | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0032others(1): Show | 4 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032-470delT | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chrX | 102320553 | |||||
| chrX:102321235
|
T | TC | 2 | a0001c0001t0001g0015a0001c0001t0001g0019 | 2 | HG02071.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1068+180dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321235 | |||||
| chrX:102321248
|
A | AC | 14 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(11): Show | 14 | HG01099.hp1 HG01433.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1069-186dupC | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321248 | |||||
| chrX:102321248
|
A | ACC | 4 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-187_1069-186d others(4): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321248 | |||||
| chrX:102321248
|
A | ACCC | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0025others(1): Show | 4 | HG00621.hp2 HG02129.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-188_1069-186d others(5): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321248 | |||||
| chrX:102321248
|
A | ACCCC | 6 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-189_1069-186d others(6): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321248 | |||||
| chrX:102321248
|
A | ACCCCCC | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1068+190_1069-186d others(8): Show |
NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chrX | 102321248 | |||||
| chrX:102321257
|
A | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069-185A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 13/22 | chrX | 102321257 | ||||||
| chrX:102321912
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+21T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 16/22 | chrX | 102321912 | ||||||
| chrX:102322406
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1477-14C>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 18/22 | chrX | 102322406 | ||||||
| chrX:102322660
|
A | C | 1 | a0001c0001t0001g0006 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1519+198A>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 19/22 | chrX | 102322660 | ||||||
| chrX:102322997
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1520-66G>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 19/22 | chrX | 102322997 | ||||||
| chrX:102323873
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1775+21G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102323873 | ||||||
| chrX:102323882
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1775+30G>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102323882 | ||||||
| chrX:102323894
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1775+42T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102323894 | ||||||
| chrX:102324150
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1775+298T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102324150 | ||||||
| chrX:102324245
|
T | A | 5 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775+393T>A | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102324245 | ||||||
| chrX:102324602
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00642.hp2 HG01099.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1775+750T>C | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102324602 | ||||||
| chrX:102324866
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0028 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1775+1014G>T | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102324866 | ||||||
| chrX:102325972
|
C | G | 1 | a0001c0002t0001g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1776-291C>G | NXF2 | ENSG00000269405.7 | transcript | ENST00000625106.4 | protein_coding | 21/22 | chrX | 102325972 |