Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2258 |
| ensemblid | ENSG00000129682.16 |
| hgncid | 3670 |
| symbol | FGF13 |
| name | fibroblast growth factor 13 |
| refseq_nuc | NM_004114.5 |
| refseq_prot | NP_004105.1 |
| ensembl_nuc | ENST00000315930.11 |
| ensembl_prot | ENSP00000322390.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 138614727 |
| end | 138711717 |
| strand | - |
| ver | v1.2 |
| region | chrX:138614727-138711717 |
| region5000 | chrX:138609727-138716717 |
| regionname0 | FGF13_chrX_138614727_138711717 |
| regionname5000 | FGF13_chrX_138609727_138716717 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 735 | 240 | 54 | 49 | 100 | 11 | 24 | FGF13_chrX_138609727_138716717 | FGF13 | ATGGC others(730): Show |
chrX | 138609727 | 138716717 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 19576 | 18 | 4 | 3 | 7 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0002 | 0/0 | 19576 | 15 | 2 | 6 | 3 | 2 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0003 | 0/0 | 19575 | 15 | 0 | 0 | 15 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0004 | 0/0 | 19602 | 11 | 0 | 4 | 7 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19597): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0005 | 0/0 | 19582 | 11 | 2 | 1 | 4 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19577): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0006 | 0/0 | 19577 | 10 | 1 | 3 | 4 | 0 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0007 | 0/0 | 19578 | 8 | 0 | 5 | 1 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0008 | 0/0 | 19572 | 7 | 1 | 2 | 0 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19567): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0009 | 0/0 | 19579 | 6 | 6 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19574): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0010 | 0/0 | 19577 | 5 | 0 | 0 | 5 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0011 | 0/0 | 19576 | 5 | 0 | 0 | 5 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0012 | 0/0 | 19576 | 4 | 0 | 4 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0013 | 0/0 | 19603 | 4 | 0 | 2 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19598): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0014 | 0/0 | 19573 | 4 | 0 | 0 | 4 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0015 | 0/0 | 19574 | 3 | 2 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0016 | 0/0 | 19577 | 3 | 3 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0017 | 0/0 | 19571 | 3 | 0 | 0 | 2 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19566): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0018 | 0/0 | 19583 | 3 | 0 | 2 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19578): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0019 | 0/0 | 19606 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19601): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0020 | 0/0 | 19573 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0021 | 0/0 | 19575 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0022 | 0/0 | 19575 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0023 | 0/0 | 19575 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0024 | 0/0 | 19574 | 2 | 0 | 0 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0025 | 0/0 | 19673 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19668): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0026 | 0/0 | 19543 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19538): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0027 | 0/0 | 19543 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19538): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0028 | 0/0 | 19569 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19564): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0029 | 0/0 | 19574 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0030 | 0/0 | 19578 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0031 | 1/0 | 19575 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0032 | 0/0 | 19575 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0033 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0034 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0035 | 0/0 | 19603 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19598): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0036 | 0/0 | 19545 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19540): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0037 | 0/0 | 19578 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0038 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0039 | 0/0 | 19577 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0040 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0041 | 0/0 | 19574 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0042 | 0/0 | 19578 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0043 | 0/0 | 19575 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0044 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0045 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0046 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0047 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0048 | 0/0 | 19604 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19599): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0049 | 0/0 | 19580 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19575): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0050 | 0/0 | 19578 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0051 | 0/0 | 19578 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0052 | 0/0 | 19579 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19574): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0053 | 0/0 | 19604 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19599): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0054 | 0/0 | 19629 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19624): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0055 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0056 | 0/0 | 19585 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19580): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0057 | 0/0 | 19578 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0058 | 0/0 | 19578 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0059 | 0/0 | 19576 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0060 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0061 | 0/0 | 19577 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0062 | 0/0 | 19577 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0063 | 0/0 | 19577 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19572): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0064 | 0/0 | 19602 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19597): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0065 | 0/0 | 19574 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0066 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0067 | 0/0 | 19575 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0068 | 0/0 | 19601 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19596): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0069 | 0/0 | 19648 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19643): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0070 | 0/0 | 19671 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19666): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0071 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0072 | 0/0 | 19574 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0073 | 0/0 | 19572 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19567): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0074 | 0/0 | 19570 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19565): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0075 | 0/0 | 19572 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19567): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0076 | 0/0 | 19573 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0077 | 0/0 | 19573 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0078 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0079 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19569): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0080 | 0/0 | 19575 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0081 | 0/0 | 19575 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0082 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0083 | 0/0 | 19545 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19540): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0084 | 0/0 | 19544 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19539): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0085 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19568): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0086 | 0/0 | 19578 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0087 | 0/0 | 19571 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19566): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0088 | 0/0 | 19578 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0089 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0090 | 0/0 | 19507 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19502): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0091 | 0/0 | 19547 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19542): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0092 | 0/0 | 19545 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19540): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0093 | 0/0 | 19545 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19540): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0094 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0095 | 0/0 | 19582 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19577): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0096 | 0/0 | 19580 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19575): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0097 | 0/0 | 19580 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19575): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0098 | 0/0 | 19578 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0099 | 0/0 | 19579 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19574): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0100 | 0/0 | 19583 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19578): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0101 | 0/0 | 19579 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19574): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0102 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19570): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0103 | 0/1 | 19629 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19624): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0104 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19571): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0105 | 0/0 | 19611 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19606): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0106 | 0/0 | 19582 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19577): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0107 | 0/0 | 19582 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19577): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0108 | 0/0 | 19609 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19604): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0109 | 0/0 | 19578 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0110 | 0/0 | 19582 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19577): Show |
chrX | 138609727 | 138716717 |
| a0001c0001t0111 | 0/0 | 19578 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | GTCGC others(19573): Show |
chrX | 138609727 | 138716717 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0012g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0017g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0017g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0018g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0018g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0019g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0020g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0021g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0021g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0022g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0023g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0024g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0024g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0025g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0026g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0027g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0028g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0029g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0030g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0030g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0031g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0032g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0033g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0034g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0035g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0036g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0037g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0038g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0039g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0040g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0041g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0042g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0043g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0044g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0045g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0046g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0047g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0048g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0049g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0050g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0051g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0052g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0053g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0054g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0055g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0056g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0057g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0058g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0059g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0060g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0061g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0062g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0063g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0064g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0065g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0066g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0067g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0068g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0069g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0070g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0071g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0072g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0073g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0074g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0075g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0076g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0077g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0078g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0079g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0080g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0081g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0082g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0083g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0084g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0085g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0086g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0087g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0088g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0089g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0090g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0091g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0092g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0093g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0094g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0095g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0096g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0097g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0098g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0099g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0100g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0101g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0102g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0103g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0104g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0105g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0106g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0107g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0108g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0109g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0110g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0111g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0202 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00323 | hp1 | a0001 | c0001 | t0057 | g0087 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00323 | hp2 | a0001 | c0001 | t0058 | g0116 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0195 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00558 | hp1 | a0001 | c0001 | t0072 | g0043 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00597 | hp1 | a0001 | c0001 | t0061 | g0055 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00609 | hp1 | a0001 | c0001 | t0030 | g0197 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00621 | hp1 | a0001 | c0001 | t0104 | g0187 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00639 | hp1 | a0001 | c0001 | t0083 | g0183 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00639 | hp2 | a0001 | c0001 | t0043 | g0133 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0004 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0004 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01071 | hp2 | a0001 | c0001 | t0062 | g0088 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01074 | hp1 | a0001 | c0001 | t0074 | g0069 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01081 | hp1 | a0001 | c0001 | t0063 | g0134 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0004 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0004 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01109 | hp1 | a0001 | c0001 | t0075 | g0178 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01167 | hp1 | a0001 | c0001 | t0042 | g0166 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0102 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01243 | hp1 | a0001 | c0001 | t0068 | g0092 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01255 | hp1 | a0001 | c0001 | t0065 | g0026 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01257 | hp2 | a0001 | c0001 | t0035 | g0050 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01261 | hp1 | a0001 | c0001 | t0080 | g0157 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0057 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01496 | hp1 | a0001 | c0001 | t0059 | g0029 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01496 | hp2 | a0001 | c0001 | t0053 | g0108 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0001 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01516 | hp2 | a0001 | c0001 | t0047 | g0056 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01884 | hp1 | a0001 | c0001 | t0027 | g0181 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01884 | hp2 | a0001 | c0001 | t0110 | g0192 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01943 | hp1 | a0001 | c0001 | t0100 | g0073 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0107 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01981 | hp1 | a0001 | c0001 | t0018 | g0011 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02004 | hp1 | a0001 | c0001 | t0048 | g0112 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02004 | hp2 | a0001 | c0001 | t0013 | g0060 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02015 | hp1 | a0001 | c0001 | t0017 | g0168 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02055 | hp1 | a0001 | c0001 | t0070 | g0160 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0198 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02074 | hp1 | a0001 | c0001 | t0102 | g0185 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02080 | hp2 | a0001 | c0001 | t0018 | g0130 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02083 | hp1 | a0001 | c0001 | t0028 | g0021 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02145 | hp1 | a0001 | c0001 | t0086 | g0163 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0070 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | CDX | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02258 | hp1 | a0001 | c0001 | t0027 | g0150 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02273 | hp1 | a0001 | c0001 | t0099 | g0072 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02273 | hp2 | a0001 | c0001 | t0049 | g0101 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02280 | hp2 | a0001 | c0001 | t0093 | g0177 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02293 | hp1 | a0001 | c0001 | t0018 | g0011 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02300 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02451 | hp1 | a0001 | c0001 | t0105 | g0191 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02451 | hp2 | a0001 | c0001 | t0036 | g0179 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0137 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0089 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02615 | hp2 | a0001 | c0001 | t0079 | g0037 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02622 | hp1 | a0001 | c0001 | t0044 | g0036 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02622 | hp2 | a0001 | c0001 | t0077 | g0176 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02698 | hp1 | a0001 | c0001 | t0033 | g0091 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02717 | hp1 | a0001 | c0001 | t0092 | g0174 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02818 | hp1 | a0001 | c0001 | t0097 | g0180 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02895 | hp1 | a0001 | c0001 | t0069 | g0161 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02896 | hp1 | a0001 | c0001 | t0091 | g0175 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02896 | hp2 | a0001 | c0001 | t0039 | g0156 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02965 | hp1 | a0001 | c0001 | t0060 | g0094 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02970 | hp1 | a0001 | c0001 | t0052 | g0031 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02976 | hp1 | a0001 | c0001 | t0084 | g0182 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02976 | hp2 | a0001 | c0001 | t0054 | g0103 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0075 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03098 | hp1 | a0001 | c0001 | t0026 | g0022 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03130 | hp1 | a0001 | c0001 | t0095 | g0040 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03195 | hp1 | a0001 | c0001 | t0026 | g0022 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03195 | hp2 | a0001 | c0001 | t0037 | g0028 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03209 | hp1 | a0001 | c0001 | t0076 | g0159 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0035 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03453 | hp1 | a0001 | c0001 | t0090 | g0032 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03453 | hp2 | a0001 | c0001 | t0089 | g0042 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03490 | hp1 | a0001 | c0001 | t0017 | g0172 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03492 | hp1 | a0001 | c0001 | t0081 | g0064 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03516 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03654 | hp1 | a0001 | c0001 | t0046 | g0061 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03669 | hp1 | a0001 | c0001 | t0041 | g0184 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03669 | hp2 | a0001 | c0001 | t0032 | g0024 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0205 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03710 | hp1 | a0001 | c0001 | t0045 | g0165 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03834 | hp2 | a0001 | c0001 | t0096 | g0154 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0201 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04199 | hp1 | a0001 | c0001 | t0109 | g0193 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0199 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04228 | hp1 | a0001 | c0001 | t0024 | g0058 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0046 | AFR | YRI | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18612 | hp1 | a0001 | c0001 | t0028 | g0021 | EAS | CHB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18747 | hp1 | a0001 | c0001 | t0024 | g0039 | EAS | CHB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0114 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18942 | hp1 | a0001 | c0001 | t0085 | g0171 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18945 | hp1 | a0001 | c0001 | t0017 | g0170 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18946 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18946 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18947 | hp1 | a0001 | c0001 | t0011 | g0076 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18947 | hp2 | a0001 | c0001 | t0101 | g0074 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18948 | hp1 | a0001 | c0001 | t0111 | g0194 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0052 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0132 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18951 | hp2 | a0001 | c0001 | t0094 | g0098 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18952 | hp1 | a0001 | c0001 | t0023 | g0143 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18953 | hp1 | a0001 | c0001 | t0082 | g0142 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18960 | hp1 | a0001 | c0001 | t0034 | g0051 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0079 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18962 | hp1 | a0001 | c0001 | t0055 | g0115 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18965 | hp1 | a0001 | c0001 | t0023 | g0148 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18971 | hp1 | a0001 | c0001 | t0010 | g0127 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18977 | hp1 | a0001 | c0001 | t0029 | g0010 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18979 | hp2 | a0001 | c0001 | t0021 | g0128 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18982 | hp1 | a0001 | c0001 | t0078 | g0136 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18983 | hp1 | a0001 | c0001 | t0019 | g0066 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18984 | hp1 | a0001 | c0001 | t0040 | g0144 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18985 | hp1 | a0001 | c0001 | t0019 | g0049 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18986 | hp1 | a0001 | c0001 | t0021 | g0106 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18988 | hp1 | a0001 | c0001 | t0022 | g0138 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18989 | hp1 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18990 | hp1 | a0001 | c0001 | t0022 | g0146 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18995 | hp1 | a0001 | c0001 | t0029 | g0010 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19000 | hp1 | a0001 | c0001 | t0108 | g0190 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19006 | hp1 | a0001 | c0001 | t0014 | g0121 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19007 | hp1 | a0001 | c0001 | t0098 | g0041 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19009 | hp1 | a0001 | c0001 | t0020 | g0122 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19030 | hp2 | a0001 | c0001 | t0088 | g0068 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19055 | hp1 | a0001 | c0001 | t0051 | g0077 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19056 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19058 | hp1 | a0001 | c0001 | t0107 | g0196 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19060 | hp1 | a0001 | c0001 | t0071 | g0124 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19063 | hp1 | a0001 | c0001 | t0020 | g0149 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19064 | hp1 | a0001 | c0001 | t0013 | g0083 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19068 | hp1 | a0001 | c0001 | t0073 | g0078 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19070 | hp1 | a0001 | c0001 | t0030 | g0200 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19072 | hp1 | a0001 | c0001 | t0087 | g0169 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19076 | hp1 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19082 | hp1 | a0001 | c0001 | t0066 | g0120 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19083 | hp1 | a0001 | c0001 | t0014 | g0119 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19084 | hp2 | a0001 | c0001 | t0011 | g0096 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19089 | hp2 | a0001 | c0001 | t0056 | g0081 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19091 | hp1 | a0001 | c0001 | t0064 | g0111 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20129 | hp1 | a0001 | c0001 | t0016 | g0129 | AFR | ASW | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20129 | hp2 | a0001 | c0001 | t0050 | g0027 | AFR | ASW | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20752 | hp1 | a0001 | c0001 | t0106 | g0203 | EUR | TSI | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | TSI | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | GIH | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02109 | hp1 | a0001 | c0001 | t0067 | g0158 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | USA | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20300 | hp2 | a0001 | c0001 | t0038 | g0099 | AFR | USA | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0103 | g0186 | REF | REF | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0031 | g0025 | REF | REF | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:138615172 | C | T | 1 | a0001c0001t0095 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17678G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17678 | chrX | 138615172 | ||||||
| chrX:138615290 | T | C | 2 | a0001c0001t0091 a0001c0001t0093 |
2 | HG02280.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17560A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17560 | chrX | 138615290 | ||||||
| chrX:138615423 | A | C | 2 | a0001c0001t0016 a0001c0001t0084 |
4 | HG02886.hp1 HG02976.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*17427T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17427 | chrX | 138615423 | ||||||
| chrX:138615476 | T | A | 3 | a0001c0001t0091 a0001c0001t0092 a0001c0001t0093 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17374A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17374 | chrX | 138615476 | ||||||
| chrX:138615604 | G | A | 1 | a0001c0001t0021 | 2 | NA18979.hp2 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17246C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17246 | chrX | 138615604 | ||||||
| chrX:138615926 | A | G | 4 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 others(1): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*16924T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 16924 | chrX | 138615926 | ||||||
| chrX:138616592 | A | G | 4 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(1): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*16258T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 16258 | chrX | 138616592 | ||||||
| chrX:138616693 | C | T | 3 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 |
5 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*16157G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 16157 | chrX | 138616693 | ||||||
| chrX:138616713 | T | C | 1 | a0001c0001t0047 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16137A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 16137 | chrX | 138616713 | ||||||
| chrX:138616926 | C | T | 1 | a0001c0001t0041 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15924G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15924 | chrX | 138616926 | ||||||
| chrX:138616960 | AG | A | 7 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0036 others(4): Show |
9 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*15889delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15889 | chrX | 138616960 | ||||||
| chrX:138617146 | T | C | 2 | a0001c0001t0043 a0001c0001t0063 |
2 | HG00639.hp2 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15704A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15704 | chrX | 138617146 | ||||||
| chrX:138617320 | T | C | 1 | a0001c0001t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15530A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15530 | chrX | 138617320 | ||||||
| chrX:138617435 | C | T | 1 | a0001c0001t0106 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15415G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15415 | chrX | 138617435 | ||||||
| chrX:138617622 | CAT | C | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(15): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*15226_*15227delAT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15226 | chrX | 138617622 | ||||||
| chrX:138617919 | G | C | 2 | a0001c0001t0105 a0001c0001t0110 |
2 | HG01884.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14931C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14931 | chrX | 138617919 | ||||||
| chrX:138617943 | C | CAG | 2 | a0001c0001t0083 a0001c0001t0091 |
2 | HG00639.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14905_*14906dupCT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14906 | chrX | 138617943 | ||||||
| chrX:138618081 | C | G | 1 | a0001c0001t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14769G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14769 | chrX | 138618081 | ||||||
| chrX:138618083 | G | A | 1 | a0001c0001t0054 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14767C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14767 | chrX | 138618083 | ||||||
| chrX:138618222 | G | C | 1 | a0001c0001t0044 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14628C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14628 | chrX | 138618222 | ||||||
| chrX:138618243 | G | A | 2 | a0001c0001t0009 a0001c0001t0052 |
7 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14607C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14607 | chrX | 138618243 | ||||||
| chrX:138618250 | G | C | 85 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(82): Show |
183 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*14600C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14600 | chrX | 138618250 | ||||||
| chrX:138618728 | G | A | 1 | a0001c0001t0034 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14122C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 14122 | chrX | 138618728 | ||||||
| chrX:138618886 | G | T | 1 | a0001c0001t0052 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13964C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13964 | chrX | 138618886 | ||||||
| chrX:138619052 | C | T | 1 | a0001c0001t0087 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13798G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13798 | chrX | 138619052 | ||||||
| chrX:138619073 | C | T | 2 | a0001c0001t0032 a0001c0001t0046 |
2 | HG03654.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13777G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13777 | chrX | 138619073 | ||||||
| chrX:138619637 | G | A | 1 | a0001c0001t0107 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13213C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13213 | chrX | 138619637 | ||||||
| chrX:138619701 | C | T | 1 | a0001c0001t0041 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13149G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13149 | chrX | 138619701 | ||||||
| chrX:138619740 | G | C | 15 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0030 others(12): Show |
28 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*13110C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13110 | chrX | 138619740 | ||||||
| chrX:138619846 | G | C | 13 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(10): Show |
40 | HG00621.hp1 HG00741.hp2 HG01069.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*13004C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13004 | chrX | 138619846 | ||||||
| chrX:138620172 | C | T | 1 | a0001c0001t0036 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12678G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 12678 | chrX | 138620172 | ||||||
| chrX:138620416 | G | A | 1 | a0001c0001t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12434C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 12434 | chrX | 138620416 | ||||||
| chrX:138620688 | A | T | 1 | a0001c0001t0077 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12162T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 12162 | chrX | 138620688 | ||||||
| chrX:138621340 | A | G | 1 | a0001c0001t0061 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11510T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11510 | chrX | 138621340 | ||||||
| chrX:138621412 | A | G | 16 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0030 others(13): Show |
29 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*11438T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11438 | chrX | 138621412 | ||||||
| chrX:138621568 | A | T | 4 | a0001c0001t0039 a0001c0001t0067 a0001c0001t0076 others(1): Show |
4 | HG01261.hp1 HG02109.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11282T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11282 | chrX | 138621568 | ||||||
| chrX:138621895 | G | C | 1 | a0001c0001t0053 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10955C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10955 | chrX | 138621895 | ||||||
| chrX:138622046 | C | G | 1 | a0001c0001t0066 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10804G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10804 | chrX | 138622046 | ||||||
| chrX:138622057 | C | CA | 41 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(38): Show |
96 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*10792dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10792 | chrX | 138622057 | ||||||
| chrX:138622472 | T | C | 1 | a0001c0001t0042 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10378A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10378 | chrX | 138622472 | ||||||
| chrX:138622563 | TGCCACTT others(33): Show |
T | 1 | a0001c0001t0056 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10247_*10286delTC others(38): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10247 | chrX | 138622563 | ||||||
| chrX:138622663 | G | T | 1 | a0001c0001t0060 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10187C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10187 | chrX | 138622663 | ||||||
| chrX:138622984 | C | T | 1 | a0001c0001t0064 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9866G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9866 | chrX | 138622984 | ||||||
| chrX:138623316 | TAAA | T | 4 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(1): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9531_*9533delTTT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9531 | chrX | 138623316 | ||||||
| chrX:138623320 | A | T | 4 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(1): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9530T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9530 | chrX | 138623320 | ||||||
| chrX:138623367 | A | T | 1 | a0001c0001t0056 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9483T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9483 | chrX | 138623367 | ||||||
| chrX:138623405 | G | GAAAGGAT others(42): Show |
1 | a0001c0001t0056 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9444_*9445insTTTT others(45): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9444 | chrX | 138623405 | ||||||
| chrX:138623408 | T | A | 1 | a0001c0001t0056 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9442A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9442 | chrX | 138623408 | ||||||
| chrX:138623416 | T | A | 1 | a0001c0001t0056 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9434A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9434 | chrX | 138623416 | ||||||
| chrX:138623538 | C | T | 6 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0036 others(3): Show |
9 | HG02015.hp1 HG02083.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9312G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9312 | chrX | 138623538 | ||||||
| chrX:138623609 | T | C | 3 | a0001c0001t0091 a0001c0001t0092 a0001c0001t0093 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9241A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9241 | chrX | 138623609 | ||||||
| chrX:138623767 | A | G | 1 | a0001c0001t0022 | 2 | NA18988.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9083T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9083 | chrX | 138623767 | ||||||
| chrX:138623831 | C | A | 1 | a0001c0001t0022 | 2 | NA18988.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9019G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9019 | chrX | 138623831 | ||||||
| chrX:138624191 | T | C | 1 | a0001c0001t0012 | 4 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8659A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8659 | chrX | 138624191 | ||||||
| chrX:138624525 | G | T | 1 | a0001c0001t0105 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8325C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8325 | chrX | 138624525 | ||||||
| chrX:138624552 | T | A | 1 | a0001c0001t0036 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8298A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8298 | chrX | 138624552 | ||||||
| chrX:138624582 | TAA | T | 2 | a0001c0001t0008 a0001c0001t0074 |
8 | HG00741.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8266_*8267delTT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8266 | chrX | 138624582 | ||||||
| chrX:138624631 | C | T | 1 | a0001c0001t0059 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8219G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8219 | chrX | 138624631 | ||||||
| chrX:138624772 | G | C | 4 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 others(1): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8078C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8078 | chrX | 138624772 | ||||||
| chrX:138624878 | G | A | 1 | a0001c0001t0023 | 2 | NA18952.hp1 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7972C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7972 | chrX | 138624878 | ||||||
| chrX:138625163 | T | C | 4 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(1): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7687A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7687 | chrX | 138625163 | ||||||
| chrX:138625433 | C | T | 8 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0036 others(5): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7417G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7417 | chrX | 138625433 | ||||||
| chrX:138625458 | T | TTATATAT others(20): Show |
10 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0019 others(7): Show |
24 | HG00558.hp2 HG00673.hp1 HG01243.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7365_*7391dupTTAT others(23): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7391 | chrX | 138625458 | ||||||
| chrX:138625458 | TTATATAT others(60): Show |
T | 1 | a0001c0001t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7325_*7391delTATA others(63): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7325 | chrX | 138625458 | ||||||
| chrX:138625471 | C | CAT | 2 | a0001c0001t0057 a0001c0001t0058 |
2 | HG00323.hp1 HG00323.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7377_*7378dupAT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7378 | chrX | 138625471 | ||||||
| chrX:138625473 | T | TATATATA others(43): Show |
1 | a0001c0001t0054 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7376_*7377insGTAT others(46): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7376 | chrX | 138625473 | ||||||
| chrX:138625483 | T | A | 1 | a0001c0001t0050 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7367A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7367 | chrX | 138625483 | ||||||
| chrX:138625483 | T | C | 4 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(1): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7367A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7367 | chrX | 138625483 | ||||||
| chrX:138625486 | T | TATATATA others(89): Show |
1 | a0001c0001t0070 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7363_*7364insTATA others(92): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7363 | chrX | 138625486 | ||||||
| chrX:138625486 | T | TATATATA others(66): Show |
1 | a0001c0001t0069 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7363_*7364insTATA others(69): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7363 | chrX | 138625486 | ||||||
| chrX:138625486 | T | TATATATA others(91): Show |
1 | a0001c0001t0025 | 2 | HG03516.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7363_*7364insTATA others(94): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7363 | chrX | 138625486 | ||||||
| chrX:138625488 | TATATATA others(21): Show |
T | 8 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0036 others(5): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7334_*7361delTATA others(24): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7334 | chrX | 138625488 | ||||||
| chrX:138625514 | A | G | 1 | a0001c0001t0059 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7336T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7336 | chrX | 138625514 | ||||||
| chrX:138625592 | C | T | 4 | a0001c0001t0036 a0001c0001t0091 a0001c0001t0092 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7258G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7258 | chrX | 138625592 | ||||||
| chrX:138625618 | T | C | 1 | a0001c0001t0071 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7232A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7232 | chrX | 138625618 | ||||||
| chrX:138625708 | A | G | 4 | a0001c0001t0011 a0001c0001t0051 a0001c0001t0056 others(1): Show |
8 | NA18946.hp2 NA18947.hp1 NA18961.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7142T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7142 | chrX | 138625708 | ||||||
| chrX:138625803 | T | C | 1 | a0001c0001t0100 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7047A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7047 | chrX | 138625803 | ||||||
| chrX:138625911 | G | A | 4 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 others(1): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6939C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6939 | chrX | 138625911 | ||||||
| chrX:138625969 | C | T | 1 | a0001c0001t0050 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6881G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6881 | chrX | 138625969 | ||||||
| chrX:138626052 | TTC | T | 4 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 others(1): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6796_*6797delGA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6796 | chrX | 138626052 | ||||||
| chrX:138626112 | G | A | 3 | a0001c0001t0091 a0001c0001t0092 a0001c0001t0093 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6738C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6738 | chrX | 138626112 | ||||||
| chrX:138626308 | A | G | 8 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0036 others(5): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6542T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6542 | chrX | 138626308 | ||||||
| chrX:138626392 | C | A | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02698.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6458G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6458 | chrX | 138626392 | ||||||
| chrX:138626405 | G | A | 1 | a0001c0001t0072 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6445C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6445 | chrX | 138626405 | ||||||
| chrX:138627208 | C | T | 1 | a0001c0001t0055 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5642G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5642 | chrX | 138627208 | ||||||
| chrX:138627209 | G | A | 8 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0036 others(5): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5641C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5641 | chrX | 138627209 | ||||||
| chrX:138627502 | G | C | 1 | a0001c0001t0109 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5348C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5348 | chrX | 138627502 | ||||||
| chrX:138627597 | C | CTG | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
86 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*5251_*5252dupCA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5252 | chrX | 138627597 | ||||||
| chrX:138627597 | C | CTGTG | 20 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0009 others(17): Show |
48 | HG00280.hp1 HG00438.hp2 HG01167.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5249_*5252dupCACA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5252 | chrX | 138627597 | ||||||
| chrX:138627597 | C | CTGTGTG | 2 | a0001c0001t0049 a0001c0001t0105 |
2 | HG02273.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5247_*5252dupCACA others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5252 | chrX | 138627597 | ||||||
| chrX:138627597 | CTG | C | 6 | a0001c0001t0073 a0001c0001t0074 a0001c0001t0075 others(3): Show |
6 | HG01074.hp1 HG01109.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5251_*5252delCA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5251 | chrX | 138627597 | ||||||
| chrX:138627624 | TGTGC | T | 2 | a0001c0001t0080 a0001c0001t0093 |
2 | HG01261.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5222_*5225delGCAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5222 | chrX | 138627624 | ||||||
| chrX:138627626 | T | C | 4 | a0001c0001t0015 a0001c0001t0030 a0001c0001t0044 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5224A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5224 | chrX | 138627626 | ||||||
| chrX:138627626 | T | TGC | 4 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0038 others(1): Show |
10 | HG00639.hp2 HG00741.hp1 HG01516.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5222_*5223dupGC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5223 | chrX | 138627626 | ||||||
| chrX:138627626 | T | TGTGC | 7 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0020 others(4): Show |
9 | HG02523.hp2 HG03453.hp1 NA18977.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5223_*5224insGCAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5223 | chrX | 138627626 | ||||||
| chrX:138627626 | T | TGTGTGC | 2 | a0001c0001t0030 a0001c0001t0099 |
2 | HG00609.hp1 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5223_*5224insGCAC others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5223 | chrX | 138627626 | ||||||
| chrX:138627626 | TGC | T | 3 | a0001c0001t0026 a0001c0001t0091 a0001c0001t0092 |
4 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5222_*5223delGC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5222 | chrX | 138627626 | ||||||
| chrX:138627626 | TGCGC | T | 3 | a0001c0001t0027 a0001c0001t0083 a0001c0001t0084 |
4 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5220_*5223delGCGC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5220 | chrX | 138627626 | ||||||
| chrX:138627628 | C | T | 8 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0079 others(5): Show |
11 | HG02015.hp1 HG02145.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5222G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5222 | chrX | 138627628 | ||||||
| chrX:138627630 | C | CGCGTGT | 1 | a0001c0001t0019 | 2 | NA18983.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5219_*5220insACAC others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5219 | chrX | 138627630 | ||||||
| chrX:138627630 | C | CGT | 9 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(6): Show |
32 | HG00621.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5218_*5219dupAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5219 | chrX | 138627630 | ||||||
| chrX:138627630 | C | T | 8 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0026 others(5): Show |
13 | HG02273.hp1 HG02523.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5220G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5220 | chrX | 138627630 | ||||||
| chrX:138627630 | CGT | C | 1 | a0001c0001t0028 | 2 | HG02083.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5218_*5219delAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5218 | chrX | 138627630 | ||||||
| chrX:138627632 | T | C | 11 | a0001c0001t0017 a0001c0001t0079 a0001c0001t0080 others(8): Show |
13 | HG01261.hp1 HG01884.hp2 HG02015.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5218A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5218 | chrX | 138627632 | ||||||
| chrX:138627634 | T | C | 4 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0083 others(1): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5216A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5216 | chrX | 138627634 | ||||||
| chrX:138627690 | C | A | 1 | a0001c0001t0098 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5160G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5160 | chrX | 138627690 | ||||||
| chrX:138627864 | A | G | 1 | a0001c0001t0043 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4986T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4986 | chrX | 138627864 | ||||||
| chrX:138628007 | C | T | 1 | a0001c0001t0033 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4843 | chrX | 138628007 | ||||||
| chrX:138628023 | G | C | 5 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0085 others(2): Show |
8 | HG02015.hp1 HG02083.hp1 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4827C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4827 | chrX | 138628023 | ||||||
| chrX:138628812 | G | T | 12 | a0001c0001t0005 a0001c0001t0030 a0001c0001t0095 others(9): Show |
23 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4038C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4038 | chrX | 138628812 | ||||||
| chrX:138628930 | T | C | 4 | a0001c0001t0042 a0001c0001t0088 a0001c0001t0089 others(1): Show |
4 | HG01167.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3920A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3920 | chrX | 138628930 | ||||||
| chrX:138628942 | A | C | 1 | a0001c0001t0042 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3908T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3908 | chrX | 138628942 | ||||||
| chrX:138629008 | T | C | 3 | a0001c0001t0091 a0001c0001t0092 a0001c0001t0093 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3842A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3842 | chrX | 138629008 | ||||||
| chrX:138630077 | T | C | 1 | a0001c0001t0029 | 2 | NA18977.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2773A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 2773 | chrX | 138630077 | ||||||
| chrX:138630217 | A | G | 1 | a0001c0001t0041 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2633T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 2633 | chrX | 138630217 | ||||||
| chrX:138630319 | C | A | 1 | a0001c0001t0111 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2531G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 2531 | chrX | 138630319 | ||||||
| chrX:138630685 | C | T | 1 | a0001c0001t0040 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 2165 | chrX | 138630685 | ||||||
| chrX:138630845 | C | T | 1 | a0001c0001t0039 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 2005 | chrX | 138630845 | ||||||
| chrX:138630907 | T | G | 1 | a0001c0001t0094 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1943A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1943 | chrX | 138630907 | ||||||
| chrX:138630928 | T | C | 17 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0030 others(14): Show |
30 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1922A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1922 | chrX | 138630928 | ||||||
| chrX:138631099 | T | TGTAA | 17 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0030 others(14): Show |
30 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1747_*1750dupTTAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1750 | chrX | 138631099 | ||||||
| chrX:138631283 | C | G | 1 | a0001c0001t0036 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1567G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1567 | chrX | 138631283 | ||||||
| chrX:138631398 | A | T | 1 | a0001c0001t0038 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1452T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1452 | chrX | 138631398 | ||||||
| chrX:138631444 | A | C | 1 | a0001c0001t0037 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1406 | chrX | 138631444 | ||||||
| chrX:138631517 | G | T | 1 | a0001c0001t0036 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1333C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1333 | chrX | 138631517 | ||||||
| chrX:138631546 | G | T | 1 | a0001c0001t0035 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1304C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1304 | chrX | 138631546 | ||||||
| chrX:138632223 | A | G | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02698.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*627T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 627 | chrX | 138632223 | ||||||
| chrX:138711025 | C | A | 1 | a0001c0001t0102 | 1 | HG02074.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-22G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | chrX | 138711025 | |||||||
| chrX:138711384 | CT | C | 108 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(105): Show |
237 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
5_prime_UTR_variant | MODIFIER | c.-382delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 382 | chrX | 138711384 | ||||||
| chrX:138711385 | T | C | 1 | a0001c0001t0032 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-382A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 382 | chrX | 138711385 | ||||||
| chrX:138711673 | G | A | 10 | a0001c0001t0005 a0001c0001t0030 a0001c0001t0104 others(7): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-670C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | chrX | 138711673 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:138633588 | A | G | 1 | a0001c0001t0093g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.602-602T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633588 | |||||||
| chrX:138633818 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.602-832C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633818 | |||||||
| chrX:138633892 | G | T | 1 | a0001c0001t0002g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.602-906C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633892 | |||||||
| chrX:138634029 | C | A | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-1043G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634029 | |||||||
| chrX:138634564 | T | C | 1 | a0001c0001t0059g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+893A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634564 | |||||||
| chrX:138634791 | C | T | 1 | a0001c0001t0004g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.601+666G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634791 | |||||||
| chrX:138634814 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.601+643A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634814 | |||||||
| chrX:138634879 | A | G | 5 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+578T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634879 | |||||||
| chrX:138634960 | C | T | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.601+497G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634960 | |||||||
| chrX:138635113 | C | G | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+344G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635113 | |||||||
| chrX:138635113 | C | T | 1 | a0001c0001t0020g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.601+344G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635113 | |||||||
| chrX:138635124 | G | A | 23 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(20): Show |
24 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.601+333C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635124 | |||||||
| chrX:138635912 | A | C | 1 | a0001c0001t0091g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403-257T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138635912 | |||||||
| chrX:138636257 | C | G | 2 | a0001c0001t0088g0068 a0001c0001t0089g0042 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403-602G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636257 | |||||||
| chrX:138636710 | A | G | 4 | a0001c0001t0002g0164 a0001c0001t0038g0099 a0001c0001t0060g0094 others(1): Show |
4 | HG02615.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1055T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636710 | |||||||
| chrX:138636929 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.403-1274A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636929 | |||||||
| chrX:138637341 | T | C | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-1686A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138637341 | |||||||
| chrX:138637639 | A | G | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-1984T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138637639 | |||||||
| chrX:138637762 | G | A | 1 | a0001c0001t0024g0039 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.403-2107C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138637762 | |||||||
| chrX:138638324 | C | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
41 | HG00558.hp1 HG00621.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.403-2669G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638324 | |||||||
| chrX:138638505 | C | G | 1 | a0001c0001t0016g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.403-2850G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638505 | |||||||
| chrX:138638527 | C | G | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-2872G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638527 | |||||||
| chrX:138638613 | G | A | 1 | a0001c0001t0049g0101 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.403-2958C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638613 | |||||||
| chrX:138638630 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-2975G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638630 | |||||||
| chrX:138638675 | T | C | 1 | a0001c0001t0007g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.403-3020A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638675 | |||||||
| chrX:138638720 | G | A | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-3065C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638720 | |||||||
| chrX:138638965 | C | A | 7 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(4): Show |
8 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-3310G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138638965 | |||||||
| chrX:138639033 | C | A | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-3378G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639033 | |||||||
| chrX:138639416 | G | A | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(197): Show |
235 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.403-3761C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639416 | |||||||
| chrX:138639565 | T | G | 1 | a0001c0001t0074g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.403-3910A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639565 | |||||||
| chrX:138639815 | C | G | 1 | a0001c0001t0082g0142 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.403-4160G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639815 | |||||||
| chrX:138639879 | G | A | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-4224C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639879 | |||||||
| chrX:138640031 | A | C | 1 | a0001c0001t0014g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.403-4376T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640031 | |||||||
| chrX:138640178 | C | T | 5 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-4523G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640178 | |||||||
| chrX:138640484 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.403-4829G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640484 | |||||||
| chrX:138640788 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.403-5133G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640788 | |||||||
| chrX:138640874 | G | A | 4 | a0001c0001t0002g0164 a0001c0001t0038g0099 a0001c0001t0060g0094 others(1): Show |
4 | HG02615.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-5219C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640874 | |||||||
| chrX:138640969 | A | G | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.403-5314T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640969 | |||||||
| chrX:138641217 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.403-5562C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138641217 | |||||||
| chrX:138641273 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.403-5618C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138641273 | |||||||
| chrX:138641436 | C | T | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-5781G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138641436 | |||||||
| chrX:138641604 | TA | T | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.403-5950delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138641604 | |||||||
| chrX:138641636 | A | C | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-5981T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138641636 | |||||||
| chrX:138642113 | C | T | 3 | a0001c0001t0002g0164 a0001c0001t0038g0099 a0001c0001t0079g0037 |
3 | HG02615.hp2 HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.403-6458G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138642113 | |||||||
| chrX:138642196 | A | G | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(197): Show |
235 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.403-6541T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138642196 | |||||||
| chrX:138642432 | G | A | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-6777C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138642432 | |||||||
| chrX:138642843 | A | G | 50 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(47): Show |
59 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.403-7188T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138642843 | |||||||
| chrX:138642894 | T | C | 1 | a0001c0001t0003g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.403-7239A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138642894 | |||||||
| chrX:138643138 | A | C | 10 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(7): Show |
11 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-7483T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643138 | |||||||
| chrX:138643160 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0093 a0001c0001t0057g0087 others(1): Show |
5 | HG00323.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-7505G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643160 | |||||||
| chrX:138643274 | C | T | 1 | a0001c0001t0091g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403-7619G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643274 | |||||||
| chrX:138643295 | T | A | 2 | a0001c0001t0005g0023 a0001c0001t0107g0196 |
3 | NA18954.hp2 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.403-7640A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643295 | |||||||
| chrX:138643388 | C | T | 2 | a0001c0001t0041g0184 a0001c0001t0075g0178 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.403-7733G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643388 | |||||||
| chrX:138643676 | T | G | 7 | a0001c0001t0011g0012 a0001c0001t0011g0076 a0001c0001t0011g0079 others(4): Show |
8 | NA18946.hp2 NA18947.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-8021A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643676 | |||||||
| chrX:138643815 | T | A | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-8160A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643815 | |||||||
| chrX:138644309 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403-8654C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138644309 | |||||||
| chrX:138644528 | C | G | 1 | a0001c0001t0097g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.403-8873G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138644528 | |||||||
| chrX:138644933 | T | C | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-9278A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138644933 | |||||||
| chrX:138645189 | T | A | 4 | a0001c0001t0027g0150 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
4 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-9534A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138645189 | |||||||
| chrX:138645606 | C | A | 7 | a0001c0001t0017g0168 a0001c0001t0017g0170 a0001c0001t0017g0172 others(4): Show |
8 | HG02015.hp1 HG02083.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-9951G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138645606 | |||||||
| chrX:138645838 | C | T | 1 | a0001c0001t0016g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.403-10183G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138645838 | |||||||
| chrX:138646395 | T | C | 4 | a0001c0001t0002g0164 a0001c0001t0038g0099 a0001c0001t0060g0094 others(1): Show |
4 | HG02615.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-10740A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138646395 | |||||||
| chrX:138646507 | A | G | 27 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(24): Show |
29 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.403-10852T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138646507 | |||||||
| chrX:138646852 | G | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
42 | HG00558.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.403-11197C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138646852 | |||||||
| chrX:138647213 | T | C | 2 | a0001c0001t0006g0018 a0001c0001t0058g0116 |
3 | HG00323.hp2 HG01358.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.403-11558A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647213 | |||||||
| chrX:138647219 | G | GA | 13 | a0001c0001t0002g0053 a0001c0001t0002g0082 a0001c0001t0002g0084 others(10): Show |
13 | HG00642.hp1 HG01106.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-11565dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647219 | |||||||
| chrX:138647219 | GAAAAAAA others(3): Show |
G | 8 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-11574_403-1156 others(14): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647219 | |||||||
| chrX:138647220 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.403-11565T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647220 | |||||||
| chrX:138647264 | T | C | 9 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(6): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-11609A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647264 | |||||||
| chrX:138647423 | C | T | 11 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(8): Show |
12 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.403-11768G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647423 | |||||||
| chrX:138647482 | A | G | 9 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(6): Show |
10 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-11827T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647482 | |||||||
| chrX:138648053 | A | T | 5 | a0001c0001t0008g0001 a0001c0001t0008g0045 a0001c0001t0008g0070 others(2): Show |
8 | HG00741.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-12398T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648053 | |||||||
| chrX:138648365 | G | C | 1 | a0001c0001t0081g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.403-12710C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648365 | |||||||
| chrX:138648461 | T | C | 1 | a0001c0001t0054g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-12806A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648461 | |||||||
| chrX:138648469 | A | G | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-12814T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648469 | |||||||
| chrX:138648622 | A | G | 5 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-12967T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648622 | |||||||
| chrX:138648748 | G | A | 1 | a0001c0001t0105g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403-13093C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648748 | |||||||
| chrX:138648817 | C | T | 1 | a0001c0001t0005g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-13162G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648817 | |||||||
| chrX:138649056 | C | G | 2 | a0001c0001t0088g0068 a0001c0001t0089g0042 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403-13401G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649056 | |||||||
| chrX:138649185 | T | C | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
208 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.403-13530A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649185 | |||||||
| chrX:138649208 | T | C | 1 | a0001c0001t0013g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.403-13553A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649208 | |||||||
| chrX:138649375 | C | G | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-13720G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649375 | |||||||
| chrX:138649487 | C | T | 1 | a0001c0001t0082g0142 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.403-13832G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649487 | |||||||
| chrX:138649559 | C | G | 1 | a0001c0001t0068g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.403-13904G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649559 | |||||||
| chrX:138649749 | G | C | 1 | a0001c0001t0017g0168 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.403-14094C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649749 | |||||||
| chrX:138649765 | G | T | 1 | a0001c0001t0094g0098 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.403-14110C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649765 | |||||||
| chrX:138649780 | A | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-14125T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649780 | |||||||
| chrX:138649850 | C | G | 1 | a0001c0001t0006g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.403-14195G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649850 | |||||||
| chrX:138649887 | A | G | 3 | a0001c0001t0017g0170 a0001c0001t0017g0172 a0001c0001t0087g0169 |
3 | HG03490.hp1 NA18945.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.403-14232T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649887 | |||||||
| chrX:138649894 | C | T | 4 | a0001c0001t0007g0002 a0001c0001t0007g0014 a0001c0001t0007g0102 others(1): Show |
8 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.403-14239G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138649894 | |||||||
| chrX:138650047 | A | G | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.403-14392T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138650047 | |||||||
| chrX:138650766 | A | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0150 a0001c0001t0027g0181 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-15111T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138650766 | |||||||
| chrX:138651492 | G | A | 1 | a0001c0001t0011g0076 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.403-15837C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138651492 | |||||||
| chrX:138651739 | C | T | 3 | a0001c0001t0041g0184 a0001c0001t0075g0178 a0001c0001t0097g0180 |
3 | HG01109.hp1 HG02818.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.403-16084G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138651739 | |||||||
| chrX:138651835 | C | A | 1 | a0001c0001t0041g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-16180G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138651835 | |||||||
| chrX:138652512 | T | C | 2 | a0001c0001t0067g0158 a0001c0001t0076g0159 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.403-16857A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138652512 | |||||||
| chrX:138652665 | G | A | 1 | a0001c0001t0046g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.403-17010C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138652665 | |||||||
| chrX:138653020 | G | C | 2 | a0001c0001t0032g0024 a0001c0001t0034g0051 |
2 | HG03669.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.403-17365C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653020 | |||||||
| chrX:138653036 | G | C | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.403-17381C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653036 | |||||||
| chrX:138653168 | C | T | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-17513G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653168 | |||||||
| chrX:138653247 | C | T | 5 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-17592G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653247 | |||||||
| chrX:138653281 | C | G | 1 | a0001c0001t0006g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.403-17626G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653281 | |||||||
| chrX:138653737 | T | G | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-18082A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653737 | |||||||
| chrX:138653854 | G | C | 1 | a0001c0001t0009g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.403-18199C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653854 | |||||||
| chrX:138653856 | C | T | 1 | a0001c0001t0089g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.403-18201G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653856 | |||||||
| chrX:138654059 | T | C | 3 | a0001c0001t0041g0184 a0001c0001t0075g0178 a0001c0001t0097g0180 |
3 | HG01109.hp1 HG02818.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.403-18404A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654059 | |||||||
| chrX:138654076 | G | GGTCT | 5 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-18425_403-1842 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654076 | |||||||
| chrX:138654387 | G | C | 5 | a0001c0001t0005g0023 a0001c0001t0005g0195 a0001c0001t0005g0198 others(2): Show |
6 | HG00438.hp2 HG02071.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-18732C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654387 | |||||||
| chrX:138654515 | C | T | 3 | a0001c0001t0041g0184 a0001c0001t0075g0178 a0001c0001t0097g0180 |
3 | HG01109.hp1 HG02818.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.403-18860G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654515 | |||||||
| chrX:138654516 | G | A | 4 | a0001c0001t0042g0166 a0001c0001t0088g0068 a0001c0001t0089g0042 others(1): Show |
4 | HG01167.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-18861C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654516 | |||||||
| chrX:138654602 | G | A | 1 | a0001c0001t0004g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.403-18947C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654602 | |||||||
| chrX:138654656 | G | A | 20 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(17): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.403-19001C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654656 | |||||||
| chrX:138654744 | A | AATAC | 72 | a0001c0001t0002g0090 a0001c0001t0003g0003 a0001c0001t0003g0008 others(69): Show |
85 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.403-19093_403-1909 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654744 | |||||||
| chrX:138654744 | A | AATACATA others(1): Show |
25 | a0001c0001t0004g0015 a0001c0001t0004g0107 a0001c0001t0004g0110 others(22): Show |
27 | HG00673.hp1 HG00735.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.403-19097_403-1909 others(12): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654744 | |||||||
| chrX:138654744 | A | AATACATA others(5): Show |
1 | a0001c0001t0022g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.403-19101_403-1909 others(16): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654744 | |||||||
| chrX:138654744 | AATAC | A | 10 | a0001c0001t0006g0135 a0001c0001t0026g0022 a0001c0001t0027g0181 others(7): Show |
11 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-19093_403-1909 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654744 | |||||||
| chrX:138654794 | G | A | 2 | a0001c0001t0041g0184 a0001c0001t0097g0180 |
2 | HG02818.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.403-19139C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654794 | |||||||
| chrX:138655109 | G | A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-19454C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655109 | |||||||
| chrX:138655216 | G | T | 1 | a0001c0001t0036g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-19561C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655216 | |||||||
| chrX:138655718 | ATAT | A | 3 | a0001c0001t0042g0166 a0001c0001t0088g0068 a0001c0001t0089g0042 |
3 | HG01167.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403-20066_403-2006 others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655718 | |||||||
| chrX:138655756 | GTTA | G | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-20104_403-2010 others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655756 | |||||||
| chrX:138655772 | A | T | 1 | a0001c0001t0054g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-20117T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655772 | |||||||
| chrX:138655941 | G | A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-20286C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138655941 | |||||||
| chrX:138656136 | T | C | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-20481A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656136 | |||||||
| chrX:138656189 | T | C | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-20534A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656189 | |||||||
| chrX:138656296 | G | C | 2 | a0001c0001t0043g0133 a0001c0001t0063g0134 |
2 | HG00639.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.403-20641C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656296 | |||||||
| chrX:138656297 | G | C | 1 | a0001c0001t0012g0004 | 4 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-20642C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656297 | |||||||
| chrX:138656336 | G | A | 1 | a0001c0001t0017g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.403-20681C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656336 | |||||||
| chrX:138656414 | C | A | 73 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(70): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.403-20759G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656414 | |||||||
| chrX:138656471 | C | T | 112 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(109): Show |
127 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.403-20816G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656471 | |||||||
| chrX:138656474 | G | A | 1 | a0001c0001t0040g0144 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.403-20819C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656474 | |||||||
| chrX:138656847 | A | G | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-21192T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138656847 | |||||||
| chrX:138657094 | A | G | 1 | a0001c0001t0026g0022 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.403-21439T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657094 | |||||||
| chrX:138657157 | T | A | 2 | a0001c0001t0004g0110 a0001c0001t0006g0145 |
2 | HG00673.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.403-21502A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657157 | |||||||
| chrX:138657158 | A | T | 1 | a0001c0001t0004g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.403-21503T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657158 | |||||||
| chrX:138657159 | G | A | 73 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(70): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.403-21504C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657159 | |||||||
| chrX:138657292 | G | C | 1 | a0001c0001t0068g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.403-21637C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657292 | |||||||
| chrX:138657553 | C | T | 1 | a0001c0001t0006g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.403-21898G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657553 | |||||||
| chrX:138657584 | C | T | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-21929G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657584 | |||||||
| chrX:138657728 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0086 |
2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.403-22073G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657728 | |||||||
| chrX:138657927 | G | A | 20 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(17): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.403-22272C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657927 | |||||||
| chrX:138658061 | T | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-22406A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138658061 | |||||||
| chrX:138658267 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403-22612A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138658267 | |||||||
| chrX:138658709 | A | C | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-23054T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138658709 | |||||||
| chrX:138658721 | C | A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-23066G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138658721 | |||||||
| chrX:138659019 | A | G | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-23364T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138659019 | |||||||
| chrX:138659199 | G | A | 73 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(70): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.403-23544C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138659199 | |||||||
| chrX:138659490 | G | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-23835C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138659490 | |||||||
| chrX:138659906 | T | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-24251A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138659906 | |||||||
| chrX:138660084 | T | A | 21 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(18): Show |
22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.403-24429A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138660084 | |||||||
| chrX:138660113 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.403-24458G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138660113 | |||||||
| chrX:138660497 | G | A | 2 | a0001c0001t0036g0179 a0001c0001t0097g0180 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.403-24842C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138660497 | |||||||
| chrX:138660763 | A | G | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-25108T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138660763 | |||||||
| chrX:138661122 | ACTACGTA others(3): Show |
A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0044 others(3): Show |
9 | HG02155.hp2 HG02523.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-25477_403-2546 others(14): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661122 | |||||||
| chrX:138661127 | G | A | 1 | a0001c0001t0056g0081 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.403-25472C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661127 | |||||||
| chrX:138661346 | G | A | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-25691C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661346 | |||||||
| chrX:138661347 | C | A | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-25692G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661347 | |||||||
| chrX:138661652 | A | G | 3 | a0001c0001t0015g0035 a0001c0001t0015g0089 a0001c0001t0044g0036 |
3 | HG02615.hp1 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.403-25997T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661652 | |||||||
| chrX:138662252 | T | C | 1 | a0001c0001t0110g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.403-26597A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138662252 | |||||||
| chrX:138663408 | A | T | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-27753T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138663408 | |||||||
| chrX:138664020 | T | G | 21 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(18): Show |
22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.403-28365A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664020 | |||||||
| chrX:138664553 | A | ATG | 2 | a0001c0001t0006g0135 a0001c0001t0078g0136 |
2 | NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.403-28900_403-2889 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664553 | |||||||
| chrX:138664558 | T | TGA | 76 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(73): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.403-28905_403-2890 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664558 | |||||||
| chrX:138664560 | A | T | 1 | a0001c0001t0074g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.403-28905T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664560 | |||||||
| chrX:138664771 | A | G | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-29116T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664771 | |||||||
| chrX:138665517 | T | G | 1 | a0001c0001t0038g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.403-29862A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138665517 | |||||||
| chrX:138665562 | G | A | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-29907C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138665562 | |||||||
| chrX:138666186 | T | A | 14 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0007g0002 others(11): Show |
19 | HG00642.hp1 HG01192.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.403-30531A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138666186 | |||||||
| chrX:138666548 | C | T | 10 | a0001c0001t0006g0016 a0001c0001t0006g0018 a0001c0001t0006g0135 others(7): Show |
12 | HG00323.hp2 HG00735.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.403-30893G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138666548 | |||||||
| chrX:138666742 | G | T | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.403-31087C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138666742 | |||||||
| chrX:138666882 | A | C | 2 | a0001c0001t0043g0133 a0001c0001t0063g0134 |
2 | HG00639.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.403-31227T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138666882 | |||||||
| chrX:138667118 | A | G | 1 | a0001c0001t0092g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.403-31463T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667118 | |||||||
| chrX:138667258 | T | A | 1 | a0001c0001t0092g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.403-31603A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667258 | |||||||
| chrX:138667272 | T | G | 21 | a0001c0001t0005g0023 a0001c0001t0005g0195 a0001c0001t0005g0198 others(18): Show |
22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.403-31617A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667272 | |||||||
| chrX:138667274 | G | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(26): Show |
38 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.403-31619C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667274 | |||||||
| chrX:138667544 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.403-31889T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667544 | |||||||
| chrX:138667860 | G | A | 1 | a0001c0001t0032g0024 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.403-32205C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667860 | |||||||
| chrX:138668040 | T | C | 1 | a0001c0001t0054g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-32385A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138668040 | |||||||
| chrX:138668105 | C | T | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-32450G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138668105 | |||||||
| chrX:138668432 | T | C | 1 | a0001c0001t0010g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.403-32777A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138668432 | |||||||
| chrX:138669592 | T | C | 3 | a0001c0001t0091g0175 a0001c0001t0092g0174 a0001c0001t0093g0177 |
3 | HG02280.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.402+33392A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138669592 | |||||||
| chrX:138669813 | G | A | 1 | a0001c0001t0064g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.402+33171C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138669813 | |||||||
| chrX:138670307 | G | A | 3 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0048g0112 |
3 | HG02004.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.402+32677C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138670307 | |||||||
| chrX:138670555 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.402+32429G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138670555 | |||||||
| chrX:138670685 | T | A | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+32299A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138670685 | |||||||
| chrX:138670776 | C | T | 14 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0007g0002 others(11): Show |
19 | HG00642.hp1 HG01192.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.402+32208G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138670776 | |||||||
| chrX:138671041 | C | CACT | 115 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(112): Show |
131 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.402+31942_402+3194 others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671041 | |||||||
| chrX:138671287 | C | T | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+31697G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671287 | |||||||
| chrX:138671363 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.402+31621A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671363 | |||||||
| chrX:138671499 | A | T | 1 | a0001c0001t0042g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.402+31485T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671499 | |||||||
| chrX:138671607 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.402+31377A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671607 | |||||||
| chrX:138671693 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0093 a0001c0001t0057g0087 others(1): Show |
5 | HG00323.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+31291G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671693 | |||||||
| chrX:138671737 | A | G | 1 | a0001c0001t0055g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.402+31247T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671737 | |||||||
| chrX:138671780 | CA | C | 77 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(74): Show |
91 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.402+31203delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671780 | |||||||
| chrX:138671872 | G | A | 2 | a0001c0001t0005g0188 a0001c0001t0005g0189 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.402+31112C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671872 | |||||||
| chrX:138672065 | A | T | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+30919T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672065 | |||||||
| chrX:138672268 | G | A | 95 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(92): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.402+30716C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672268 | |||||||
| chrX:138672421 | C | T | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+30563G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672421 | |||||||
| chrX:138672521 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0093 a0001c0001t0057g0087 others(1): Show |
5 | HG00323.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+30463G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672521 | |||||||
| chrX:138672687 | G | A | 1 | a0001c0001t0074g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.402+30297C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672687 | |||||||
| chrX:138672837 | C | G | 1 | a0001c0001t0043g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.402+30147G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672837 | |||||||
| chrX:138672841 | A | C | 1 | a0001c0001t0091g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.402+30143T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672841 | |||||||
| chrX:138673006 | T | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+29978A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138673006 | |||||||
| chrX:138673195 | A | G | 12 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.402+29789T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138673195 | |||||||
| chrX:138673357 | G | C | 3 | a0001c0001t0027g0181 a0001c0001t0083g0183 a0001c0001t0084g0182 |
3 | HG00639.hp1 HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.402+29627C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138673357 | |||||||
| chrX:138673505 | T | C | 1 | a0001c0001t0077g0176 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.402+29479A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138673505 | |||||||
| chrX:138673776 | A | G | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+29208T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138673776 | |||||||
| chrX:138674215 | A | G | 1 | a0001c0001t0010g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.402+28769T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138674215 | |||||||
| chrX:138675263 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.402+27721G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138675263 | |||||||
| chrX:138675581 | T | A | 1 | a0001c0001t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.402+27403A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138675581 | |||||||
| chrX:138676577 | G | A | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+26407C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138676577 | |||||||
| chrX:138676597 | A | T | 2 | a0001c0001t0032g0024 a0001c0001t0034g0051 |
2 | HG03669.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.402+26387T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138676597 | |||||||
| chrX:138676638 | G | A | 2 | a0001c0001t0003g0147 a0001c0001t0023g0148 |
2 | NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.402+26346C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138676638 | |||||||
| chrX:138676746 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.402+26238C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138676746 | |||||||
| chrX:138677230 | G | T | 1 | a0001c0001t0050g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.402+25754C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138677230 | |||||||
| chrX:138677320 | G | C | 1 | a0001c0001t0055g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.402+25664C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138677320 | |||||||
| chrX:138677475 | G | T | 1 | a0001c0001t0016g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.402+25509C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138677475 | |||||||
| chrX:138677693 | C | G | 8 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0204 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+25291G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138677693 | |||||||
| chrX:138678096 | G | A | 1 | a0001c0001t0072g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.402+24888C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678096 | |||||||
| chrX:138678134 | A | T | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+24850T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678134 | |||||||
| chrX:138678541 | T | C | 1 | a0001c0001t0089g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.402+24443A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678541 | |||||||
| chrX:138678787 | G | A | 1 | a0001c0001t0003g0034 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.402+24197C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678787 | |||||||
| chrX:138678944 | C | T | 20 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(17): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+24040G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678944 | |||||||
| chrX:138678987 | G | A | 1 | a0001c0001t0072g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.402+23997C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678987 | |||||||
| chrX:138679064 | A | G | 1 | a0001c0001t0092g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402+23920T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679064 | |||||||
| chrX:138679312 | C | A | 1 | a0001c0001t0013g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.402+23672G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679312 | |||||||
| chrX:138679379 | C | A | 2 | a0001c0001t0030g0197 a0001c0001t0030g0200 |
2 | HG00609.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.402+23605G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679379 | |||||||
| chrX:138679552 | A | C | 1 | a0001c0001t0003g0117 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.402+23432T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679552 | |||||||
| chrX:138679565 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.402+23419G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679565 | |||||||
| chrX:138679649 | C | A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+23335G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679649 | |||||||
| chrX:138679787 | G | C | 1 | a0001c0001t0011g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.402+23197C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679787 | |||||||
| chrX:138679883 | T | C | 3 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0010g0127 |
3 | HG02970.hp2 HG03516.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.402+23101A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679883 | |||||||
| chrX:138679977 | A | G | 1 | a0001c0001t0003g0117 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.402+23007T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138679977 | |||||||
| chrX:138680385 | G | C | 1 | a0001c0001t0002g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.402+22599C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138680385 | |||||||
| chrX:138680669 | T | C | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+22315A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138680669 | |||||||
| chrX:138681120 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.402+21864C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681120 | |||||||
| chrX:138681166 | C | CA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0002g0093 others(12): Show |
18 | HG00738.hp1 HG02055.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.402+21817dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681166 | |||||||
| chrX:138681166 | CA | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0173 a0001c0001t0006g0131 others(2): Show |
5 | HG00741.hp2 HG01346.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+21817delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681166 | |||||||
| chrX:138681225 | T | G | 1 | a0001c0001t0093g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.402+21759A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681225 | |||||||
| chrX:138681291 | C | G | 1 | a0001c0001t0013g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.402+21693G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681291 | |||||||
| chrX:138681407 | AAG | A | 71 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(68): Show |
84 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.402+21575_402+2157 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681407 | |||||||
| chrX:138681427 | C | G | 1 | a0001c0001t0005g0023 | 2 | NA18954.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.402+21557G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681427 | |||||||
| chrX:138681502 | A | C | 1 | a0001c0001t0016g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.402+21482T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681502 | |||||||
| chrX:138681817 | G | A | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+21167C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681817 | |||||||
| chrX:138681847 | A | C | 1 | a0001c0001t0066g0120 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.402+21137T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138681847 | |||||||
| chrX:138682453 | T | G | 1 | a0001c0001t0005g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.402+20531A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138682453 | |||||||
| chrX:138682944 | T | C | 1 | a0001c0001t0060g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.402+20040A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138682944 | |||||||
| chrX:138683401 | T | A | 1 | a0001c0001t0083g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.402+19583A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138683401 | |||||||
| chrX:138683415 | T | TCA | 8 | a0001c0001t0002g0164 a0001c0001t0020g0149 a0001c0001t0026g0022 others(5): Show |
9 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+19567_402+1956 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138683415 | |||||||
| chrX:138683417 | A | T | 2 | a0001c0001t0035g0050 a0001c0001t0058g0116 |
2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.402+19567T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138683417 | |||||||
| chrX:138683704 | A | G | 4 | a0001c0001t0042g0166 a0001c0001t0088g0068 a0001c0001t0089g0042 others(1): Show |
4 | HG01167.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+19280T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138683704 | |||||||
| chrX:138684511 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.402+18473T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138684511 | |||||||
| chrX:138684545 | A | G | 20 | a0001c0001t0003g0003 a0001c0001t0003g0104 a0001c0001t0003g0117 others(17): Show |
26 | HG00438.hp1 HG00558.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.402+18439T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138684545 | |||||||
| chrX:138684967 | G | A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+18017C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138684967 | |||||||
| chrX:138685742 | A | T | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+17242T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138685742 | |||||||
| chrX:138685806 | G | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0086 |
2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.402+17178C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138685806 | |||||||
| chrX:138686354 | G | A | 2 | a0001c0001t0005g0188 a0001c0001t0005g0189 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.402+16630C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138686354 | |||||||
| chrX:138686997 | A | C | 1 | a0001c0001t0108g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.402+15987T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138686997 | |||||||
| chrX:138687004 | T | C | 113 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(110): Show |
129 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.402+15980A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687004 | |||||||
| chrX:138687145 | A | G | 1 | a0001c0001t0014g0119 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.402+15839T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687145 | |||||||
| chrX:138687243 | C | A | 1 | a0001c0001t0005g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.402+15741G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687243 | |||||||
| chrX:138687731 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.402+15253G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687731 | |||||||
| chrX:138687841 | C | A | 1 | a0001c0001t0005g0023 | 2 | NA18954.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.402+15143G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687841 | |||||||
| chrX:138687941 | C | A | 1 | a0001c0001t0009g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.402+15043G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687941 | |||||||
| chrX:138687953 | A | AT | 7 | a0001c0001t0001g0048 a0001c0001t0002g0084 a0001c0001t0002g0085 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.402+15030dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687953 | |||||||
| chrX:138687992 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0173 |
2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.402+14992G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687992 | |||||||
| chrX:138688049 | G | A | 3 | a0001c0001t0009g0151 a0001c0001t0009g0153 a0001c0001t0027g0150 |
3 | HG02258.hp1 HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.402+14935C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688049 | |||||||
| chrX:138688446 | A | G | 1 | a0001c0001t0042g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.402+14538T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688446 | |||||||
| chrX:138688608 | C | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(170): Show |
203 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.402+14376G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688608 | |||||||
| chrX:138688835 | C | T | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+14149G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688835 | |||||||
| chrX:138688940 | T | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+14044A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688940 | |||||||
| chrX:138688960 | C | T | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+14024G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688960 | |||||||
| chrX:138689356 | T | C | 1 | a0001c0001t0005g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+13628A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138689356 | |||||||
| chrX:138689488 | G | A | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+13496C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138689488 | |||||||
| chrX:138689902 | C | T | 1 | a0001c0001t0016g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.402+13082G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138689902 | |||||||
| chrX:138690223 | C | G | 75 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(72): Show |
89 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.402+12761G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138690223 | |||||||
| chrX:138691023 | T | C | 1 | a0001c0001t0041g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+11961A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691023 | |||||||
| chrX:138691134 | C | A | 1 | a0001c0001t0030g0200 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.402+11850G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691134 | |||||||
| chrX:138691382 | G | A | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+11602C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691382 | |||||||
| chrX:138691552 | G | A | 71 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(68): Show |
84 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.402+11432C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691552 | |||||||
| chrX:138691568 | C | T | 4 | a0001c0001t0003g0104 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG00438.hp1 NA18951.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+11416G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691568 | |||||||
| chrX:138691622 | C | T | 1 | a0001c0001t0058g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.402+11362G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691622 | |||||||
| chrX:138691925 | C | A | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+11059G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691925 | |||||||
| chrX:138692045 | T | G | 20 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(17): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+10939A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692045 | |||||||
| chrX:138692401 | T | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+10583A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692401 | |||||||
| chrX:138692642 | C | T | 1 | a0001c0001t0041g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+10342G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692642 | |||||||
| chrX:138692720 | A | ATG | 5 | a0001c0001t0008g0001 a0001c0001t0008g0045 a0001c0001t0008g0070 others(2): Show |
8 | HG00558.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.402+10262_402+1026 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692720 | |||||||
| chrX:138692747 | T | C | 1 | a0001c0001t0026g0022 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.402+10237A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692747 | |||||||
| chrX:138693324 | T | A | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+9660A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138693324 | |||||||
| chrX:138693544 | G | A | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+9440C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138693544 | |||||||
| chrX:138693714 | T | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0077g0176 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+9270A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138693714 | |||||||
| chrX:138693775 | G | T | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+9209C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138693775 | |||||||
| chrX:138694360 | G | A | 1 | a0001c0001t0006g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+8624C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694360 | |||||||
| chrX:138694450 | T | TA | 3 | a0001c0001t0027g0181 a0001c0001t0083g0183 a0001c0001t0084g0182 |
3 | HG00639.hp1 HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.402+8533_402+8534i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694450 | |||||||
| chrX:138694451 | C | A | 1 | a0001c0001t0026g0022 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.402+8533G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694451 | |||||||
| chrX:138694451 | C | T | 3 | a0001c0001t0027g0181 a0001c0001t0083g0183 a0001c0001t0084g0182 |
3 | HG00639.hp1 HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.402+8533G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694451 | |||||||
| chrX:138694537 | G | A | 2 | a0001c0001t0010g0114 a0001c0001t0010g0152 |
2 | NA18940.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.402+8447C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694537 | |||||||
| chrX:138694986 | A | AAC | 18 | a0001c0001t0002g0067 a0001c0001t0004g0105 a0001c0001t0004g0107 others(15): Show |
18 | HG01255.hp1 HG01346.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.402+7996_402+7997d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | A | AACAC | 25 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0003g0008 others(22): Show |
32 | HG00597.hp2 HG00642.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.402+7994_402+7997d others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AAC | A | 25 | a0001c0001t0002g0095 a0001c0001t0004g0015 a0001c0001t0005g0199 others(22): Show |
29 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.402+7996_402+7997d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACAC | A | 5 | a0001c0001t0003g0003 a0001c0001t0005g0188 a0001c0001t0005g0202 others(2): Show |
5 | HG00280.hp1 HG02132.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+7994_402+7997d others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACAC | A | 25 | a0001c0001t0001g0167 a0001c0001t0005g0023 a0001c0001t0005g0189 others(22): Show |
26 | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.402+7992_402+7997d others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACACA others(1): Show |
A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.402+7990_402+7997d others(10): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACACA others(3): Show |
A | 1 | a0001c0001t0089g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.402+7988_402+7997d others(12): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACACA others(7): Show |
A | 2 | a0001c0001t0006g0131 a0001c0001t0006g0145 |
2 | HG00735.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.402+7984_402+7997d others(16): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACACA others(9): Show |
A | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.402+7982_402+7997d others(18): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138694986 | AACACACA others(15): Show |
A | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+7976_402+7997d others(24): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | |||||||
| chrX:138695033 | A | ACACAC | 3 | a0001c0001t0004g0110 a0001c0001t0023g0143 a0001c0001t0051g0077 |
3 | HG00673.hp1 NA18952.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.402+7950_402+7951i others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695033 | |||||||
| chrX:138695363 | C | T | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+7621G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695363 | |||||||
| chrX:138696121 | A | C | 2 | a0001c0001t0006g0016 a0001c0001t0055g0115 |
3 | NA18954.hp1 NA18962.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.402+6863T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696121 | |||||||
| chrX:138696469 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.402+6515A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696469 | |||||||
| chrX:138696556 | G | C | 3 | a0001c0001t0042g0166 a0001c0001t0088g0068 a0001c0001t0089g0042 |
3 | HG01167.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.402+6428C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696556 | |||||||
| chrX:138696626 | T | G | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+6358A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696626 | |||||||
| chrX:138696796 | C | T | 1 | a0001c0001t0089g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.402+6188G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696796 | |||||||
| chrX:138696819 | GGCTTTTC others(39): Show |
G | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+6119_402+6164d others(48): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696819 | |||||||
| chrX:138697495 | C | A | 1 | a0001c0001t0041g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+5489G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697495 | |||||||
| chrX:138697646 | A | T | 12 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.402+5338T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697646 | |||||||
| chrX:138698082 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0044 |
4 | NA18966.hp1 NA18979.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+4902T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698082 | |||||||
| chrX:138698164 | G | A | 1 | a0001c0001t0009g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.402+4820C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698164 | |||||||
| chrX:138698216 | T | C | 1 | a0001c0001t0065g0026 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.402+4768A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698216 | |||||||
| chrX:138698284 | T | C | 5 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0204 others(2): Show |
5 | HG00280.hp1 HG01256.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+4700A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698284 | |||||||
| chrX:138698340 | A | T | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4644T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698340 | |||||||
| chrX:138698632 | G | A | 1 | a0001c0001t0096g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.402+4352C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698632 | |||||||
| chrX:138699066 | T | G | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3918A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699066 | |||||||
| chrX:138699068 | A | T | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3916T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699068 | |||||||
| chrX:138699069 | C | A | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3915G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699069 | |||||||
| chrX:138699124 | T | C | 1 | a0001c0001t0065g0026 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.402+3860A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699124 | |||||||
| chrX:138699625 | C | A | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(5): Show |
9 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+3359G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699625 | |||||||
| chrX:138699695 | C | T | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3289G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699695 | |||||||
| chrX:138699696 | T | A | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3288A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699696 | |||||||
| chrX:138699697 | C | G | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3287G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699697 | |||||||
| chrX:138699700 | C | A | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3284G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699700 | |||||||
| chrX:138699703 | G | T | 1 | a0001c0001t0010g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3281C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699703 | |||||||
| chrX:138699712 | A | G | 4 | a0001c0001t0036g0179 a0001c0001t0041g0184 a0001c0001t0075g0178 others(1): Show |
4 | HG01109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+3272T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699712 | |||||||
| chrX:138699791 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.402+3193A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699791 | |||||||
| chrX:138699844 | C | A | 1 | a0001c0001t0045g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.402+3140G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699844 | |||||||
| chrX:138700388 | G | A | 1 | a0001c0001t0088g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.402+2596C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700388 | |||||||
| chrX:138700397 | G | T | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(5): Show |
9 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+2587C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700397 | |||||||
| chrX:138700539 | G | A | 1 | a0001c0001t0007g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.402+2445C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700539 | |||||||
| chrX:138700632 | G | C | 20 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(17): Show |
21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+2352C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700632 | |||||||
| chrX:138700905 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.402+2079G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700905 | |||||||
| chrX:138700983 | C | T | 19 | a0001c0001t0005g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(16): Show |
20 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.402+2001G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700983 | |||||||
| chrX:138701128 | A | G | 1 | a0001c0001t0042g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.402+1856T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701128 | |||||||
| chrX:138701179 | T | C | 1 | a0001c0001t0011g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.402+1805A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701179 | |||||||
| chrX:138701321 | C | G | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+1663G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701321 | |||||||
| chrX:138701511 | G | T | 4 | a0001c0001t0007g0002 a0001c0001t0007g0014 a0001c0001t0007g0102 others(1): Show |
8 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+1473C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701511 | |||||||
| chrX:138702098 | C | T | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+886G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702098 | |||||||
| chrX:138702165 | C | A | 1 | a0001c0001t0074g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.402+819G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702165 | |||||||
| chrX:138702191 | A | T | 3 | a0001c0001t0042g0166 a0001c0001t0072g0043 a0001c0001t0089g0042 |
3 | HG00558.hp1 HG01167.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.402+793T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702191 | |||||||
| chrX:138702195 | A | T | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(84): Show |
98 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.402+789T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702195 | |||||||
| chrX:138702199 | T | A | 11 | a0001c0001t0002g0097 a0001c0001t0002g0164 a0001c0001t0027g0181 others(8): Show |
11 | HG00639.hp1 HG01261.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+785A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702199 | |||||||
| chrX:138702247 | T | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+737A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702247 | |||||||
| chrX:138702376 | T | C | 3 | a0001c0001t0025g0020 a0001c0001t0069g0161 a0001c0001t0070g0160 |
4 | HG02055.hp1 HG02895.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+608A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702376 | |||||||
| chrX:138702382 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.402+602A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702382 | |||||||
| chrX:138702399 | T | C | 4 | a0001c0001t0007g0002 a0001c0001t0007g0014 a0001c0001t0007g0102 others(1): Show |
8 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+585A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702399 | |||||||
| chrX:138702448 | A | G | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+536T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702448 | |||||||
| chrX:138702450 | G | C | 1 | a0001c0001t0006g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+534C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702450 | |||||||
| chrX:138702496 | T | C | 4 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0083g0183 others(1): Show |
5 | HG00639.hp1 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+488A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702496 | |||||||
| chrX:138702778 | A | T | 1 | a0001c0001t0098g0041 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.402+206T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702778 | |||||||
| chrX:138702795 | C | T | 1 | a0001c0001t0095g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.402+189G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702795 | |||||||
| chrX:138703207 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0024g0039 |
2 | HG02155.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.299-120T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138703207 | |||||||
| chrX:138704362 | T | C | 1 | a0001c0001t0041g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.299-1275A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138704362 | |||||||
| chrX:138705500 | C | T | 2 | a0001c0001t0005g0188 a0001c0001t0005g0189 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.299-2413G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138705500 | |||||||
| chrX:138705616 | C | T | 3 | a0001c0001t0015g0035 a0001c0001t0044g0036 a0001c0001t0079g0037 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-2529G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138705616 | |||||||
| chrX:138705617 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-2530C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138705617 | |||||||
| chrX:138705803 | T | G | 12 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-2716A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138705803 | |||||||
| chrX:138705994 | C | G | 1 | a0001c0001t0054g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.298+2824G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138705994 | |||||||
| chrX:138706095 | T | C | 4 | a0001c0001t0077g0176 a0001c0001t0091g0175 a0001c0001t0092g0174 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+2723A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706095 | |||||||
| chrX:138706186 | CG | C | 92 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0033 others(89): Show |
106 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.298+2631delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706186 | |||||||
| chrX:138706274 | T | C | 1 | a0001c0001t0086g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298+2544A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706274 | |||||||
| chrX:138706590 | C | T | 2 | a0001c0001t0003g0033 a0001c0001t0003g0034 |
2 | NA19086.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.298+2228G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706590 | |||||||
| chrX:138706633 | A | G | 1 | a0001c0001t0090g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.298+2185T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706633 | |||||||
| chrX:138706911 | C | T | 1 | a0001c0001t0052g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+1907G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706911 | |||||||
| chrX:138707268 | T | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
48 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.298+1550A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707268 | |||||||
| chrX:138707303 | C | T | 10 | a0001c0001t0002g0030 a0001c0001t0017g0168 a0001c0001t0017g0170 others(7): Show |
11 | HG01496.hp1 HG02015.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+1515G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707303 | |||||||
| chrX:138707637 | T | C | 8 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(5): Show |
9 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+1181A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707637 | |||||||
| chrX:138707655 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298+1163A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707655 | |||||||
| chrX:138707894 | T | C | 1 | a0001c0001t0012g0004 | 4 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+924A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707894 | |||||||
| chrX:138708357 | C | A | 1 | a0001c0001t0045g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+461G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138708357 | |||||||
| chrX:138708968 | T | C | 1 | a0001c0001t0042g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.188-40A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138708968 | |||||||
| chrX:138709564 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-636A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138709564 | |||||||
| chrX:138709937 | C | G | 1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.187+880G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138709937 | |||||||
| chrX:138710014 | T | G | 6 | a0001c0001t0017g0168 a0001c0001t0017g0170 a0001c0001t0017g0172 others(3): Show |
7 | HG02015.hp1 HG02083.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+803A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710014 | |||||||
| chrX:138710404 | A | T | 1 | a0001c0001t0065g0026 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.187+413T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710404 | |||||||
| chrX:138710471 | G | A | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.187+346C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710471 | |||||||
| chrX:138710647 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+170A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710647 | |||||||
| chrX:138710805 | G | A | 12 | a0001c0001t0026g0022 a0001c0001t0027g0181 a0001c0001t0036g0179 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+12C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710805 |