Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 245 | 239 | 54 | 49 | 99 | 11 | 24 | 72 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0002 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 18837 | 17 | 4 | 3 | 6 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0002 | 0/0 | 18836 | 14 | 0 | 0 | 14 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0003 | 0/0 | 18837 | 13 | 1 | 6 | 3 | 1 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0004 | 0/0 | 18843 | 11 | 2 | 1 | 4 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0005 | 0/0 | 18863 | 10 | 0 | 4 | 6 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0006 | 0/0 | 18839 | 8 | 0 | 5 | 1 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0007 | 0/0 | 18838 | 7 | 1 | 1 | 4 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0008 | 0/0 | 18835 | 7 | 1 | 2 | 0 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0009 | 0/0 | 18838 | 5 | 0 | 0 | 5 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0010 | 0/0 | 18840 | 5 | 5 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0011 | 0/0 | 18864 | 4 | 0 | 2 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0012 | 0/0 | 18837 | 3 | 0 | 3 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0013 | 0/0 | 18837 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0014 | 0/0 | 18838 | 3 | 3 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0015 | 0/0 | 18844 | 3 | 0 | 2 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0016 | 0/0 | 18838 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0017 | 0/0 | 18835 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0018 | 0/0 | 18837 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0019 | 0/0 | 18836 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0020 | 0/0 | 18836 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0021 | 0/0 | 18836 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0022 | 0/0 | 18835 | 2 | 0 | 0 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0023 | 0/0 | 18834 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0024 | 0/0 | 18802 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0025 | 0/0 | 18832 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0026 | 0/0 | 18830 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0027 | 0/0 | 18839 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0028 | 0/0 | 18836 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0029 | 0/0 | 18837 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0030 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0031 | 0/0 | 18836 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0032 | 0/0 | 18835 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0033 | 0/0 | 18862 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0034 | 0/0 | 18835 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0035 | 0/0 | 18864 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0036 | 0/0 | 18796 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0037 | 0/0 | 18839 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0038 | 0/0 | 18837 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0039 | 0/0 | 18838 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0040 | 0/0 | 18836 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0041 | 0/0 | 18834 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0042 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0043 | 0/0 | 18833 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0044 | 0/0 | 18839 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0045 | 0/0 | 18838 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0046 | 0/0 | 18868 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0047 | 0/0 | 18867 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0048 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0049 | 0/0 | 18837 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0050 | 0/0 | 18837 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0051 | 0/0 | 18837 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0052 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0053 | 0/0 | 18865 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0054 | 0/0 | 18835 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0055 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0056 | 0/0 | 18839 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0057 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0058 | 0/0 | 18837 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0059 | 0/0 | 18840 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0060 | 0/0 | 18865 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0061 | 0/0 | 18890 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0062 | 0/0 | 18836 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0063 | 0/0 | 18836 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0064 | 0/0 | 18831 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0065 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0066 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0067 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0068 | 0/0 | 18838 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0069 | 0/0 | 18838 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0070 | 0/0 | 18834 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0071 | 0/0 | 18863 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0072 | 0/0 | 18835 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0073 | 0/0 | 18836 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0074 | 0/0 | 18835 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0075 | 0/0 | 18834 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0076 | 0/0 | 18836 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0077 | 0/0 | 18862 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0078 | 0/0 | 18909 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0079 | 0/0 | 18934 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0080 | 0/0 | 18937 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0081 | 0/0 | 18933 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0082 | 0/0 | 18833 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0083 | 0/0 | 18831 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0084 | 0/0 | 18833 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0085 | 0/0 | 18838 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0086 | 0/0 | 18834 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0087 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0088 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0089 | 0/0 | 18835 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0090 | 0/0 | 18834 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0091 | 0/0 | 18832 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0092 | 0/0 | 18836 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0093 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0094 | 0/0 | 18802 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0095 | 0/0 | 18801 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0096 | 0/0 | 18800 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0097 | 0/0 | 18831 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0098 | 0/0 | 18834 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0099 | 0/0 | 18839 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0100 | 0/0 | 18832 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0101 | 0/0 | 18831 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0102 | 0/0 | 18839 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0103 | 0/0 | 18837 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0104 | 0/0 | 18772 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0105 | 0/0 | 18806 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0106 | 0/0 | 18804 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0107 | 0/0 | 18802 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0108 | 0/0 | 18833 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0109 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0110 | 0/0 | 18836 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0111 | 0/0 | 18843 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0112 | 0/0 | 18841 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0113 | 0/0 | 18843 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0114 | 0/0 | 18843 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0115 | 0/0 | 18846 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0116 | 0/0 | 18844 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0117 | 0/0 | 18840 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0118 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0119 | 1/0 | 18838 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0120 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0121 | 0/1 | 18892 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0122 | 0/0 | 18873 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0123 | 0/0 | 18843 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0124 | 0/0 | 18843 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0125 | 0/0 | 18870 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0126 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0127 | 0/0 | 18845 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0128 | 0/0 | 18835 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0129 | 0/0 | 18845 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| t0130 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 738 | 239 | 54 | 49 | 99 | 11 | 24 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0002c0002 | 0/0 | 737 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 19574 | 17 | 4 | 3 | 6 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0002 | 0/0 | 19573 | 14 | 0 | 0 | 14 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0003 | 0/0 | 19574 | 13 | 1 | 6 | 3 | 1 | 2 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0004 | 0/0 | 19580 | 11 | 2 | 1 | 4 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0005 | 0/0 | 19600 | 10 | 0 | 4 | 6 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0006 | 0/0 | 19576 | 8 | 0 | 5 | 1 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0007 | 0/0 | 19575 | 7 | 1 | 1 | 4 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0008 | 0/0 | 19572 | 7 | 1 | 2 | 0 | 1 | 3 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0009 | 0/0 | 19575 | 5 | 0 | 0 | 5 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0010 | 0/0 | 19577 | 5 | 5 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0011 | 0/0 | 19601 | 4 | 0 | 2 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0012 | 0/0 | 19574 | 3 | 0 | 3 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0013 | 0/0 | 19574 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0014 | 0/0 | 19575 | 3 | 3 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0015 | 0/0 | 19581 | 3 | 0 | 2 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0016 | 0/0 | 19575 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0017 | 0/0 | 19572 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0018 | 0/0 | 19574 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0019 | 0/0 | 19573 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0020 | 0/0 | 19573 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0021 | 0/0 | 19573 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0022 | 0/0 | 19572 | 2 | 0 | 0 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0023 | 0/0 | 19571 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0024 | 0/0 | 19539 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0025 | 0/0 | 19569 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0026 | 0/0 | 19567 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0027 | 0/0 | 19576 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0028 | 0/0 | 19573 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0029 | 0/0 | 19574 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0030 | 0/0 | 19574 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0031 | 0/0 | 19573 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0032 | 0/0 | 19572 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0033 | 0/0 | 19599 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0034 | 0/0 | 19572 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0035 | 0/0 | 19601 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0036 | 0/0 | 19533 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0037 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0038 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0039 | 0/0 | 19575 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0040 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0041 | 0/0 | 19571 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0042 | 0/0 | 19578 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0043 | 0/0 | 19570 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0044 | 0/0 | 19576 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0045 | 0/0 | 19575 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0046 | 0/0 | 19605 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0047 | 0/0 | 19604 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0048 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0049 | 0/0 | 19574 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0050 | 0/0 | 19574 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0051 | 0/0 | 19574 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0052 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0053 | 0/0 | 19602 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0054 | 0/0 | 19572 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0055 | 0/0 | 19578 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0056 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0057 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0058 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0059 | 0/0 | 19577 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0060 | 0/0 | 19602 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0061 | 0/0 | 19627 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0062 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0063 | 0/0 | 19573 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0064 | 0/0 | 19568 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0065 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0066 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0067 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0068 | 0/0 | 19575 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0069 | 0/0 | 19575 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0070 | 0/0 | 19571 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0071 | 0/0 | 19600 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0072 | 0/0 | 19572 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0073 | 0/0 | 19573 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0074 | 0/0 | 19572 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0075 | 0/0 | 19571 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0076 | 0/0 | 19573 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0077 | 0/0 | 19599 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0078 | 0/0 | 19646 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0079 | 0/0 | 19671 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0080 | 0/0 | 19674 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0081 | 0/0 | 19670 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0082 | 0/0 | 19570 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0083 | 0/0 | 19568 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0084 | 0/0 | 19570 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0085 | 0/0 | 19575 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0086 | 0/0 | 19571 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0087 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0088 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0089 | 0/0 | 19572 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0090 | 0/0 | 19571 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0091 | 0/0 | 19569 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0092 | 0/0 | 19573 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0093 | 0/0 | 19538 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0094 | 0/0 | 19539 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0095 | 0/0 | 19538 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0096 | 0/0 | 19537 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0097 | 0/0 | 19568 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0098 | 0/0 | 19571 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0099 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0100 | 0/0 | 19569 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0101 | 0/0 | 19568 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0102 | 0/0 | 19576 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0103 | 0/0 | 19574 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0104 | 0/0 | 19509 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0105 | 0/0 | 19543 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0106 | 0/0 | 19541 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0107 | 0/0 | 19539 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0109 | 0/0 | 19574 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0110 | 0/0 | 19573 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0111 | 0/0 | 19580 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0112 | 0/0 | 19578 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0113 | 0/0 | 19580 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0114 | 0/0 | 19580 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0115 | 0/0 | 19583 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0116 | 0/0 | 19581 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0117 | 0/0 | 19577 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0118 | 0/0 | 19575 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0119 | 1/0 | 19575 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0120 | 0/0 | 19574 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0121 | 0/1 | 19629 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0122 | 0/0 | 19610 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0123 | 0/0 | 19580 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0124 | 0/0 | 19580 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0125 | 0/0 | 19607 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0126 | 0/0 | 19576 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0127 | 0/0 | 19582 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0128 | 0/0 | 19572 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0129 | 0/0 | 19582 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0001c0001t0130 | 0/0 | 19576 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| a0002c0002t0108 | 0/0 | 19569 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | copy fasta | chrX | 138609727 | 138716717 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0012g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0017g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0018g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0018g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0019g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0020g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0020g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0022g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0022g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0023g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0023g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0024g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0025g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0025g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0026g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0026g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0027g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0028g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0029g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0030g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0031g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0032g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0033g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0034g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0035g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0036g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0037g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0038g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0039g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0040g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0041g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0042g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0043g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0044g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0045g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0046g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0047g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0048g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0049g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0050g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0051g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0052g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0053g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0054g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0055g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0056g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0057g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0058g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0059g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0060g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0061g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0062g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0063g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0064g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0065g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0066g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0067g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0068g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0069g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0070g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0071g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0072g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0073g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0074g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0075g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0076g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0077g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0078g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0079g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0080g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0081g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0082g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0083g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0084g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0085g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0086g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0087g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0088g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0089g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0090g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0091g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0092g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0093g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0094g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0095g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0096g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0097g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0098g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0099g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0100g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0101g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0102g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0103g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0104g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0105g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0106g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0107g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0109g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0110g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0111g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0112g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0113g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0114g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0115g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0116g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0117g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0118g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0119g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0120g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0121g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0122g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0123g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0124g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0125g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0126g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0127g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0128g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0129g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0001c0001t0130g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| a0002c0002t0108g0024 | 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 | t0043 | g0054 | EUR | GBR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0213 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00323 | hp1 | a0001 | c0001 | t0065 | g0055 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00323 | hp2 | a0001 | c0001 | t0066 | g0116 | EUR | FIN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00558 | hp1 | a0001 | c0001 | t0097 | g0146 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00597 | hp1 | a0001 | c0001 | t0067 | g0161 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00609 | hp1 | a0001 | c0001 | t0127 | g0209 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00621 | hp1 | a0001 | c0001 | t0120 | g0217 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00639 | hp1 | a0001 | c0001 | t0094 | g0196 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00639 | hp2 | a0001 | c0001 | t0045 | g0118 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | CHS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00735 | hp1 | a0001 | c0001 | t0018 | g0126 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0138 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0059 | 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 | g0186 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01069 | hp1 | a0001 | c0001 | t0031 | g0175 | 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 | t0068 | g0056 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01074 | hp1 | a0001 | c0001 | t0083 | g0032 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01081 | hp1 | a0001 | c0001 | t0069 | g0119 | 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 | t0003 | g0052 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01109 | hp1 | a0001 | c0001 | t0084 | g0193 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01167 | hp1 | a0001 | c0001 | t0044 | g0177 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0067 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01243 | hp1 | a0001 | c0001 | t0077 | g0058 | AMR | PUR | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01255 | hp1 | a0001 | c0001 | t0074 | g0017 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0219 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01257 | hp2 | a0001 | c0001 | t0035 | g0157 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01261 | hp1 | a0001 | c0001 | t0091 | g0132 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0120 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0152 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01496 | hp1 | a0001 | c0001 | t0032 | g0022 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01496 | hp2 | a0001 | c0001 | t0060 | g0070 | AMR | CLM | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0007 | 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 | t0051 | g0153 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | IBS | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01884 | hp1 | a0001 | c0001 | t0096 | g0194 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01884 | hp2 | a0001 | c0001 | t0129 | g0204 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01943 | hp1 | a0001 | c0001 | t0116 | g0051 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0075 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0087 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01981 | hp1 | a0001 | c0001 | t0015 | g0050 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02004 | hp1 | a0001 | c0001 | t0053 | g0074 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0163 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02015 | hp1 | a0001 | c0001 | t0025 | g0179 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02055 | hp1 | a0001 | c0001 | t0081 | g0135 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02074 | hp1 | a0001 | c0001 | t0118 | g0198 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0080 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02080 | hp2 | a0001 | c0001 | t0015 | g0117 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02083 | hp1 | a0001 | c0001 | t0026 | g0180 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02145 | hp1 | a0001 | c0001 | t0099 | g0140 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0048 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | CDX | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02258 | hp1 | a0001 | c0001 | t0093 | g0123 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02273 | hp1 | a0001 | c0001 | t0115 | g0049 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02273 | hp2 | a0001 | c0001 | t0055 | g0066 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0127 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02280 | hp2 | a0001 | c0001 | t0107 | g0190 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02293 | hp1 | a0001 | c0001 | t0015 | g0035 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02451 | hp1 | a0001 | c0001 | t0122 | g0211 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02451 | hp2 | a0001 | c0001 | t0036 | g0191 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02523 | hp2 | a0001 | c0001 | t0048 | g0166 | EAS | KHV | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02572 | hp1 | a0001 | c0001 | t0058 | g0114 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0110 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0060 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02615 | hp2 | a0001 | c0001 | t0089 | g0141 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02622 | hp1 | a0001 | c0001 | t0054 | g0143 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02622 | hp2 | a0001 | c0001 | t0110 | g0189 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02698 | hp1 | a0001 | c0001 | t0029 | g0047 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02717 | hp1 | a0001 | c0001 | t0106 | g0187 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0043 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02818 | hp1 | a0001 | c0001 | t0113 | g0192 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02818 | hp2 | a0001 | c0001 | t0072 | g0174 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0072 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02895 | hp1 | a0001 | c0001 | t0078 | g0139 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02896 | hp1 | a0001 | c0001 | t0105 | g0188 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02896 | hp2 | a0001 | c0001 | t0039 | g0131 | AFR | GWD | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02965 | hp1 | a0001 | c0001 | t0073 | g0046 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02970 | hp1 | a0001 | c0001 | t0059 | g0023 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02976 | hp1 | a0001 | c0001 | t0095 | g0195 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02976 | hp2 | a0001 | c0001 | t0061 | g0068 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0044 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03098 | hp1 | a0001 | c0001 | t0024 | g0014 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03130 | hp1 | a0001 | c0001 | t0111 | g0026 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03195 | hp1 | a0001 | c0001 | t0024 | g0014 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03195 | hp2 | a0001 | c0001 | t0037 | g0020 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03209 | hp1 | a0001 | c0001 | t0085 | g0130 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0142 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03453 | hp1 | a0001 | c0001 | t0104 | g0185 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03453 | hp2 | a0001 | c0001 | t0103 | g0028 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03490 | hp1 | a0001 | c0001 | t0101 | g0184 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03492 | hp1 | a0001 | c0001 | t0092 | g0168 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03516 | hp1 | a0001 | c0001 | t0080 | g0137 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | ESN | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03579 | hp1 | a0001 | c0001 | t0079 | g0136 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03654 | hp1 | a0001 | c0001 | t0050 | g0164 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03669 | hp1 | a0001 | c0001 | t0041 | g0197 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03669 | hp2 | a0001 | c0001 | t0028 | g0016 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03688 | hp1 | a0001 | c0001 | t0070 | g0121 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03710 | hp1 | a0001 | c0001 | t0049 | g0176 | 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 | t0112 | g0128 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04199 | hp1 | a0001 | c0001 | t0126 | g0205 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG04228 | hp1 | a0001 | c0001 | t0022 | g0162 | SAS | STU | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0154 | AFR | YRI | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18612 | hp1 | a0001 | c0001 | t0026 | g0182 | EAS | CHB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18747 | hp1 | a0001 | c0001 | t0022 | g0145 | EAS | CHB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18940 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18942 | hp1 | a0001 | c0001 | t0098 | g0181 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18942 | hp2 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18945 | hp1 | a0001 | c0001 | t0025 | g0183 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18946 | hp1 | a0001 | c0001 | t0023 | g0102 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18946 | hp2 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18947 | hp1 | a0001 | c0001 | t0013 | g0037 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18947 | hp2 | a0001 | c0001 | t0117 | g0034 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18948 | hp1 | a0001 | c0001 | t0130 | g0206 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18951 | hp1 | a0001 | c0001 | t0033 | g0076 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18951 | hp2 | a0001 | c0001 | t0109 | g0065 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18952 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18953 | hp1 | a0001 | c0001 | t0090 | g0094 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18960 | hp1 | a0001 | c0001 | t0030 | g0158 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18961 | hp1 | a0001 | c0001 | t0013 | g0038 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18962 | hp1 | a0001 | c0001 | t0062 | g0082 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18965 | hp1 | a0001 | c0001 | t0021 | g0089 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18977 | hp1 | a0001 | c0001 | t0027 | g0013 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18979 | hp2 | a0001 | c0001 | t0019 | g0107 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18982 | hp1 | a0001 | c0001 | t0086 | g0109 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18983 | hp1 | a0001 | c0001 | t0047 | g0170 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18984 | hp1 | a0001 | c0001 | t0040 | g0112 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18985 | hp1 | a0001 | c0001 | t0046 | g0151 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18986 | hp1 | a0001 | c0001 | t0019 | g0078 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18988 | hp1 | a0001 | c0001 | t0020 | g0093 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18989 | hp1 | a0001 | c0001 | t0009 | g0115 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18990 | hp1 | a0001 | c0001 | t0020 | g0113 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18992 | hp2 | a0001 | c0001 | t0052 | g0147 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA18995 | hp1 | a0001 | c0001 | t0027 | g0013 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19000 | hp1 | a0001 | c0001 | t0125 | g0203 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19006 | hp1 | a0001 | c0001 | t0087 | g0099 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19007 | hp1 | a0001 | c0001 | t0114 | g0027 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19009 | hp1 | a0001 | c0001 | t0016 | g0095 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19030 | hp2 | a0001 | c0001 | t0102 | g0031 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19055 | hp1 | a0001 | c0001 | t0057 | g0033 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19056 | hp1 | a0001 | c0001 | t0034 | g0100 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19058 | hp1 | a0001 | c0001 | t0124 | g0208 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19060 | hp1 | a0001 | c0001 | t0088 | g0103 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19063 | hp1 | a0001 | c0001 | t0016 | g0090 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19064 | hp1 | a0001 | c0001 | t0011 | g0171 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19068 | hp1 | a0001 | c0001 | t0082 | g0045 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19070 | hp1 | a0001 | c0001 | t0128 | g0212 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19072 | hp1 | a0001 | c0001 | t0100 | g0018 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19076 | hp1 | a0001 | c0001 | t0042 | g0039 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19082 | hp1 | a0001 | c0001 | t0075 | g0091 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19083 | hp1 | a0001 | c0001 | t0023 | g0098 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19084 | hp2 | a0001 | c0001 | t0063 | g0062 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19086 | hp1 | a0002 | c0002 | t0108 | g0024 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19089 | hp2 | a0001 | c0001 | t0064 | g0036 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA19091 | hp1 | a0001 | c0001 | t0071 | g0073 | EAS | JPT | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0092 | AFR | ASW | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20129 | hp2 | a0001 | c0001 | t0056 | g0019 | AFR | ASW | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20752 | hp1 | a0001 | c0001 | t0123 | g0215 | EUR | TSI | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0057 | 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 | t0076 | g0133 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | ACB | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | USA | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA20300 | hp2 | a0001 | c0001 | t0038 | g0064 | AFR | USA | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | LWK | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0121 | g0216 | REF | REF | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0119 | g0199 | REF | REF | FGF13_chrX_138609727_138716717 | FGF13 | chrX | 138609727 | 138716717 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:138632981
|
TG | T | 1 | a0002 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.606delC | p.Met203fs | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1320/19575 | 606/738 | 202/245 | chrX | 138632981 |
| 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 |
|---|
| 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:138614876
|
C | CACA | 1 | a0001c0001t0080 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17971_*17973dupTG others(1): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 17973 | chrX | 138614876 | |||||
| chrX:138615172
|
C | T | 1 | a0001c0001t0111 | 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 | a0001c0001t0105a0001c0001t0107 | 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 | a0001c0001t0014a0001c0001t0095 | 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 | a0001c0001t0105a0001c0001t0106a0001c0001t0107 | 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 | a0001c0001t0019 | 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 | 5 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(2): 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 | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(2): 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 | 4 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(1): Show | 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 | a0001c0001t0051 | 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
|
A | AG | 2 | a0001c0001t0122a0001c0001t0129 | 2 | HG01884.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15889dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 15889 | chrX | 138616960 | |||||
| chrX:138616960
|
AG | A | 8 | a0001c0001t0024a0001c0001t0036a0001c0001t0093others(5): 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 | a0001c0001t0045a0001c0001t0069 | 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 | a0001c0001t0104 | 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 | a0001c0001t0123 | 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 | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(20): 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 | a0001c0001t0122a0001c0001t0129 | 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 | a0001c0001t0094a0001c0001t0105 | 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 | a0001c0001t0104 | 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 | a0001c0001t0061 | 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 | a0001c0001t0054 | 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 | 3 | a0001c0001t0010a0001c0001t0058a0001c0001t0059 | 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 | 100 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(97): 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 | a0001c0001t0030 | 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 | a0001c0001t0059 | 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 | a0001c0001t0100 | 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 | a0001c0001t0028a0001c0001t0050 | 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:138619246
|
A | AAAAC | 1 | a0001c0001t0085 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13600_*13603dupGT others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13603 | chrX | 138619246 | |||||
| chrX:138619246
|
AAAAC | A | 2 | a0001c0001t0036a0001c0001t0070 | 2 | HG02451.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13600_*13603delGT others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13600 | chrX | 138619246 | |||||
| chrX:138619624
|
GA | G | 1 | a0001c0001t0018 | 2 | HG00735.hp1 HG00735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13225delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 13225 | chrX | 138619624 | |||||
| chrX:138619637
|
G | A | 1 | a0001c0001t0124 | 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 | 16 | a0001c0001t0004a0001c0001t0015a0001c0001t0111others(13): 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 | 16 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(13): 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:138620315
|
A | AG | 2 | a0001c0001t0046a0001c0001t0081 | 2 | HG02055.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12534dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 12534 | chrX | 138620315 | |||||
| chrX:138620416
|
G | A | 1 | a0001c0001t0104 | 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:138620492
|
TA | T | 1 | a0001c0001t0063 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12357delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 12357 | chrX | 138620492 | |||||
| chrX:138620688
|
A | T | 1 | a0001c0001t0110 | 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 | a0001c0001t0067 | 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 | 17 | a0001c0001t0004a0001c0001t0015a0001c0001t0111others(14): 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:138621502
|
G | GA | 2 | a0001c0001t0052a0001c0001t0129 | 2 | HG01884.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11347dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11347 | chrX | 138621502 | |||||
| chrX:138621502
|
GA | G | 1 | a0001c0001t0041 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11347delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11347 | chrX | 138621502 | |||||
| chrX:138621568
|
A | T | 4 | a0001c0001t0039a0001c0001t0076a0001c0001t0085others(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:138621683
|
AC | A | 1 | a0001c0001t0032 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11166delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 11166 | chrX | 138621683 | |||||
| chrX:138621895
|
G | C | 1 | a0001c0001t0060 | 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 | a0001c0001t0075 | 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 | 50 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(47): 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 | a0001c0001t0044 | 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 | a0001c0001t0064 | 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 | a0001c0001t0073 | 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:138622796
|
A | AT | 1 | a0001c0001t0093 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10053dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10053 | chrX | 138622796 | |||||
| chrX:138622796
|
AT | A | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10053delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10053 | chrX | 138622796 | |||||
| chrX:138622830
|
A | AT | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10019dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 10019 | chrX | 138622830 | |||||
| chrX:138622984
|
C | T | 1 | a0001c0001t0071 | 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:138623260
|
A | AT | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9589dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9589 | chrX | 138623260 | |||||
| chrX:138623316
|
TAAA | T | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(2): 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 | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(2): 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:138623361
|
ATT | A | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9487_*9488delAA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9487 | chrX | 138623361 | |||||
| chrX:138623367
|
A | T | 1 | a0001c0001t0064 | 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 | a0001c0001t0064 | 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 | a0001c0001t0064 | 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:138623411
|
AC | A | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9438delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9438 | chrX | 138623411 | |||||
| chrX:138623416
|
T | A | 1 | a0001c0001t0064 | 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:138623424
|
CAA | C | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9424_*9425delTT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9424 | chrX | 138623424 | |||||
| chrX:138623430
|
CAACAT | C | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9415_*9419delATGT others(1): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9415 | chrX | 138623430 | |||||
| chrX:138623475
|
CA | C | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9374delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9374 | chrX | 138623475 | |||||
| chrX:138623538
|
C | T | 7 | a0001c0001t0025a0001c0001t0026a0001c0001t0036others(4): 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 | a0001c0001t0105a0001c0001t0106a0001c0001t0107 | 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:138623614
|
TA | T | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9235delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 9235 | chrX | 138623614 | |||||
| chrX:138623767
|
A | G | 1 | a0001c0001t0020 | 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 | a0001c0001t0020 | 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:138623876
|
TA | T | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8973delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8973 | chrX | 138623876 | |||||
| chrX:138623932
|
AT | A | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8917delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8917 | chrX | 138623932 | |||||
| chrX:138624191
|
T | C | 2 | a0001c0001t0012a0001c0001t0031 | 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 | a0001c0001t0122 | 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 | a0001c0001t0008a0001c0001t0083 | 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 | a0001c0001t0032 | 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:138624666
|
GC | G | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8183delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 8183 | chrX | 138624666 | |||||
| chrX:138624772
|
G | C | 5 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(2): 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 | a0001c0001t0021 | 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:138625124
|
AC | A | 1 | a0001c0001t0064 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7725delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7725 | chrX | 138625124 | |||||
| chrX:138625163
|
T | C | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(2): 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 | 9 | a0001c0001t0024a0001c0001t0036a0001c0001t0093others(6): 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 |
12 | a0001c0001t0005a0001c0001t0011a0001c0001t0033others(9): 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 | a0001c0001t0104 | 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:138625461
|
T | TATATATA others(48): Show |
1 | a0001c0001t0121 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7334_*7388dupTATA others(51): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7388 | chrX | 138625461 | |||||
| chrX:138625471
|
C | CAT | 2 | a0001c0001t0065a0001c0001t0066 | 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 | a0001c0001t0061 | 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 | a0001c0001t0056 | 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 | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(2): 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:138625484
|
A | AAT | 1 | a0001c0001t0118 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7364_*7365dupAT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7365 | chrX | 138625484 | |||||
| chrX:138625486
|
T | TATATATA others(89): Show |
1 | a0001c0001t0081 | 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 | a0001c0001t0078 | 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 |
2 | a0001c0001t0079a0001c0001t0080 | 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 | 9 | a0001c0001t0024a0001c0001t0036a0001c0001t0093others(6): 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:138625498
|
CAT | C | 1 | a0001c0001t0072 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7350_*7351delAT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7350 | chrX | 138625498 | |||||
| chrX:138625508
|
TATA | T | 1 | a0001c0001t0058 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7339_*7341delTAT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7339 | chrX | 138625508 | |||||
| chrX:138625514
|
A | G | 1 | a0001c0001t0032 | 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 | a0001c0001t0036a0001c0001t0105a0001c0001t0106others(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 | a0001c0001t0088 | 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 | 6 | a0001c0001t0013a0001c0001t0042a0001c0001t0057others(3): 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:138625718
|
AC | A | 1 | a0001c0001t0101 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7131delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 7131 | chrX | 138625718 | |||||
| chrX:138625803
|
T | C | 1 | a0001c0001t0116 | 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 | 5 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(2): 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 | a0001c0001t0056 | 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 | 5 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(2): 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 | a0001c0001t0105a0001c0001t0106a0001c0001t0107 | 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 | 9 | a0001c0001t0024a0001c0001t0036a0001c0001t0093others(6): 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 | a0001c0001t0029a0001c0001t0030 | 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 | a0001c0001t0097 | 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:138626488
|
AT | A | 1 | a0001c0001t0073 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6361delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 6361 | chrX | 138626488 | |||||
| chrX:138627208
|
C | T | 1 | a0001c0001t0062 | 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 | 9 | a0001c0001t0024a0001c0001t0036a0001c0001t0093others(6): 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 | a0001c0001t0126 | 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:138627584
|
A | AGT | 1 | a0001c0001t0113 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5264_*5265dupAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5265 | chrX | 138627584 | |||||
| chrX:138627597
|
C | CTG | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(36): Show | 87 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(84): 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 | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(18): 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 | a0001c0001t0055a0001c0001t0122 | 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 | a0001c0001t0082a0001c0001t0083a0001c0001t0084others(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:138627597
|
CTGTG | C | 1 | a0001c0001t0128 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5249_*5252delCACA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5249 | chrX | 138627597 | |||||
| chrX:138627622
|
TGTGTGC | T | 1 | a0001c0001t0036 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5222_*5227delGCAC others(2): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5222 | chrX | 138627622 | |||||
| chrX:138627624
|
TGTGC | T | 2 | a0001c0001t0091a0001c0001t0107 | 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 | a0001c0001t0017a0001c0001t0054a0001c0001t0128others(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 | a0001c0001t0008a0001c0001t0034a0001c0001t0038others(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 | a0001c0001t0016a0001c0001t0027a0001c0001t0048others(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 | a0001c0001t0115a0001c0001t0127 | 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 | a0001c0001t0024a0001c0001t0105a0001c0001t0106 | 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 | 4 | a0001c0001t0093a0001c0001t0094a0001c0001t0095others(1): Show | 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 | 10 | a0001c0001t0025a0001c0001t0046a0001c0001t0047others(7): 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 | 2 | a0001c0001t0046a0001c0001t0047 | 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 | 11 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(8): 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 | 9 | a0001c0001t0016a0001c0001t0017a0001c0001t0024others(6): 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 | a0001c0001t0026 | 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:138627630
|
CGTGT | C | 1 | a0001c0001t0097 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5216_*5219delACAC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 5216 | chrX | 138627630 | |||||
| chrX:138627632
|
T | C | 12 | a0001c0001t0025a0001c0001t0089a0001c0001t0090others(9): 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 | 5 | a0001c0001t0024a0001c0001t0093a0001c0001t0094others(2): 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 | a0001c0001t0114 | 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 | a0001c0001t0045 | 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 | a0001c0001t0029 | 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 | 6 | a0001c0001t0025a0001c0001t0026a0001c0001t0098others(3): 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:138628774
|
TG | T | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4075delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4075 | chrX | 138628774 | |||||
| chrX:138628804
|
AG | A | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4045delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 4045 | chrX | 138628804 | |||||
| chrX:138628812
|
G | T | 13 | a0001c0001t0004a0001c0001t0111a0001c0001t0112others(10): 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:138628858
|
TG | T | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3991delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3991 | chrX | 138628858 | |||||
| chrX:138628904
|
AG | A | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3945delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3945 | chrX | 138628904 | |||||
| chrX:138628930
|
T | C | 4 | a0001c0001t0044a0001c0001t0102a0001c0001t0103others(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 | a0001c0001t0044 | 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 | a0001c0001t0105a0001c0001t0106a0001c0001t0107 | 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:138629082
|
G | GC | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3767_*3768insG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3767 | chrX | 138629082 | |||||
| chrX:138629117
|
T | TC | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3732dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3732 | chrX | 138629117 | |||||
| chrX:138629278
|
TAAAC | T | 1 | a0001c0001t0043 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3568_*3571delGTTT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3568 | chrX | 138629278 | |||||
| chrX:138629428
|
AG | A | 1 | a0002c0002t0108 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3421delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3421 | chrX | 138629428 | |||||
| chrX:138629649
|
C | CTCTT | 1 | a0001c0001t0042 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3197_*3200dupAAGA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 3200 | chrX | 138629649 | |||||
| chrX:138630077
|
T | C | 1 | a0001c0001t0027 | 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 | a0001c0001t0130 | 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 | a0001c0001t0109 | 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 | 18 | a0001c0001t0004a0001c0001t0015a0001c0001t0111others(15): 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:138631023
|
T | TAA | 1 | a0001c0001t0110 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1825_*1826dupTT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 1826 | chrX | 138631023 | |||||
| chrX:138631099
|
T | TGTAA | 18 | a0001c0001t0004a0001c0001t0015a0001c0001t0111others(15): 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:138632175
|
TA | T | 4 | a0001c0001t0031a0001c0001t0032a0001c0001t0033others(1): Show | 4 | HG01069.hp1 HG01496.hp1 NA18951.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*674delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 5/5 | 674 | chrX | 138632175 | |||||
| chrX:138632223
|
A | G | 2 | a0001c0001t0029a0001c0001t0030 | 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 | a0001c0001t0118 | 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:138711261
|
GC | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-259delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 259 | chrX | 138711261 | |||||
| chrX:138711287
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-284G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | chrX | 138711287 | ||||||
| chrX:138711293
|
T | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-290A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 290 | chrX | 138711293 | |||||
| chrX:138711296
|
T | A | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-293A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | chrX | 138711296 | ||||||
| chrX:138711315
|
T | C | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-312A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 312 | chrX | 138711315 | |||||
| chrX:138711342
|
C | T | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-339G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 339 | chrX | 138711342 | |||||
| chrX:138711348
|
T | A | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-345A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | chrX | 138711348 | ||||||
| chrX:138711352
|
C | CA | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-350dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 350 | chrX | 138711352 | |||||
| chrX:138711355
|
C | T | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-352G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 352 | chrX | 138711355 | |||||
| chrX:138711356
|
T | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-353A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 353 | chrX | 138711356 | |||||
| chrX:138711361
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-358G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 358 | chrX | 138711361 | |||||
| chrX:138711366
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-363G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 363 | chrX | 138711366 | |||||
| chrX:138711369
|
A | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-366T>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 366 | chrX | 138711369 | |||||
| chrX:138711376
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-373G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 373 | chrX | 138711376 | |||||
| chrX:138711378
|
G | C | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-375C>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 375 | chrX | 138711378 | |||||
| chrX:138711384
|
CT | C | 128 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(125): Show | 238 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(235): 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 | a0001c0001t0028 | 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:138711392
|
GT | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-390delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 390 | chrX | 138711392 | |||||
| chrX:138711398
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-395G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 395 | chrX | 138711398 | |||||
| chrX:138711399
|
T | C | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-396A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 396 | chrX | 138711399 | |||||
| chrX:138711400
|
T | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-397A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 397 | chrX | 138711400 | |||||
| chrX:138711402
|
T | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-399A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 399 | chrX | 138711402 | |||||
| chrX:138711404
|
AT | A | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-402delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 402 | chrX | 138711404 | |||||
| chrX:138711480
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-477G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 477 | chrX | 138711480 | |||||
| chrX:138711491
|
C | G | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-488G>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/5 | 488 | chrX | 138711491 | |||||
| chrX:138711673
|
G | A | 12 | a0001c0001t0004a0001c0001t0120a0001c0001t0121others(9): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): 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 |
| 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:138633005
|
TG | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-20delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633005 | ||||||
| chrX:138633025
|
TG | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-40delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633025 | ||||||
| chrX:138633210
|
TA | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-225delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633210 | ||||||
| chrX:138633321
|
G | GA | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-336dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633321 | ||||||
| chrX:138633332
|
CT | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-347delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633332 | ||||||
| chrX:138633588
|
A | G | 1 | a0001c0001t0107g0190 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0003g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.602-906C>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633892 | ||||||
| chrX:138633928
|
TA | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-943delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138633928 | ||||||
| chrX:138634029
|
C | A | 1 | a0001c0001t0036g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-1043G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634029 | ||||||
| chrX:138634190
|
A | AT | 1 | a0001c0001t0007g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.602-1205dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634190 | ||||||
| chrX:138634190
|
AT | A | 3 | a0001c0001t0017g0060a0001c0001t0017g0142a0001c0001t0054g0143 | 3 | HG02615.hp1 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.602-1205delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634190 | ||||||
| chrX:138634201
|
CT | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-1216delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634201 | ||||||
| chrX:138634345
|
TG | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+1111delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634345 | ||||||
| chrX:138634564
|
T | C | 1 | a0001c0001t0032g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+893A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634564 | ||||||
| chrX:138634699
|
ATACCACC others(1): Show |
A | 1 | a0001c0001t0098g0181 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.601+750_601+757del others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634699 | ||||||
| chrX:138634740
|
CA | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+716delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634740 | ||||||
| chrX:138634791
|
C | T | 1 | a0001c0001t0005g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.601+666G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634791 | ||||||
| chrX:138634806
|
TA | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+650delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634806 | ||||||
| chrX:138634814
|
T | G | 1 | a0001c0001t0001g0156 | 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 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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:138634969
|
A | AT | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+487dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138634969 | ||||||
| chrX:138635113
|
C | G | 1 | a0001c0001t0036g0191 | 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 | a0001c0001t0016g0095 | 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 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(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:138635143
|
AT | A | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+313delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635143 | ||||||
| chrX:138635284
|
TG | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+172delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635284 | ||||||
| chrX:138635304
|
TG | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+152delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635304 | ||||||
| chrX:138635348
|
CT | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+108delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635348 | ||||||
| chrX:138635442
|
CA | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+14delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 4/4 | chrX | 138635442 | ||||||
| chrX:138635755
|
TA | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-101delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138635755 | ||||||
| chrX:138635849
|
GA | G | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-195delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138635849 | ||||||
| chrX:138635912
|
A | C | 1 | a0001c0001t0105g0188 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403-257T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138635912 | ||||||
| chrX:138636105
|
AG | A | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-451delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636105 | ||||||
| chrX:138636198
|
ATTT | A | 1 | a0001c0001t0104g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-546_403-544del others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636198 | ||||||
| chrX:138636257
|
C | G | 2 | a0001c0001t0102g0031a0001c0001t0103g0028 | 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:138636259
|
TC | T | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-605delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636259 | ||||||
| chrX:138636473
|
C | CA | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-819dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636473 | ||||||
| chrX:138636491
|
CA | C | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-837delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636491 | ||||||
| chrX:138636710
|
A | G | 4 | a0001c0001t0038g0064a0001c0001t0072g0174a0001c0001t0073g0046others(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:138636737
|
C | CA | 1 | a0002c0002t0108g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.403-1083dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138636737 | ||||||
| chrX:138636929
|
T | C | 1 | a0001c0001t0001g0148 | 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 | a0001c0001t0036g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-1686A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138637341 | ||||||
| chrX:138637423
|
AT | A | 1 | a0001c0001t0036g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-1769delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138637423 | ||||||
| chrX:138637639
|
A | G | 1 | a0001c0001t0036g0191 | 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 | a0001c0001t0022g0145 | 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 | 35 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(32): 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 | a0001c0001t0014g0072 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0055g0066 | 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 | a0001c0001t0003g0021 | 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 | a0001c0001t0006g0007 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0099g0140 | 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 | 215 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(212): Show | 236 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(233): 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 | a0001c0001t0083g0032 | 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 | a0001c0001t0090g0094 | 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 | a0001c0001t0104g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-4224C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639879 | ||||||
| chrX:138639995
|
TA | T | 1 | a0001c0001t0102g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-4341delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138639995 | ||||||
| chrX:138640031
|
A | C | 1 | a0001c0001t0087g0099 | 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 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0038g0064a0001c0001t0072g0174a0001c0001t0073g0046others(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:138640956
|
A | AT | 1 | a0001c0001t0106g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.403-5302dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640956 | ||||||
| chrX:138640956
|
AT | A | 1 | a0001c0001t0011g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.403-5302delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138640956 | ||||||
| chrX:138640969
|
A | G | 3 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0038g0064a0001c0001t0072g0174a0001c0001t0089g0141 | 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 | 215 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(212): Show | 236 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(233): 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 | a0001c0001t0099g0140 | 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 | 55 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(52): 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0061g0068others(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 | a0001c0001t0003g0006a0001c0001t0003g0059a0001c0001t0065g0055others(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:138643193
|
A | AT | 1 | a0001c0001t0056g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.403-7539dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643193 | ||||||
| chrX:138643274
|
C | T | 1 | a0001c0001t0105g0188 | 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 | a0001c0001t0004g0015a0001c0001t0124g0208 | 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 | a0001c0001t0041g0197a0001c0001t0084g0193 | 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 | 8 | a0001c0001t0013g0037a0001c0001t0013g0038a0001c0001t0013g0040others(5): 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 | a0001c0001t0036g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-8160A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138643815 | ||||||
| chrX:138644273
|
A | AT | 1 | a0001c0001t0006g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.403-8619dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138644273 | ||||||
| chrX:138644273
|
AT | A | 1 | a0001c0001t0073g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.403-8619delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138644273 | ||||||
| chrX:138644309
|
G | A | 1 | a0001c0001t0001g0165 | 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 | a0001c0001t0113g0192 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0093g0123a0001c0001t0094g0196a0001c0001t0095g0195others(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:138645399
|
CCCT | C | 1 | a0001c0001t0001g0005 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.403-9747_403-9745d others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138645399 | ||||||
| chrX:138645606
|
C | A | 8 | a0001c0001t0025g0179a0001c0001t0025g0183a0001c0001t0026g0180others(5): 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 | a0001c0001t0014g0092 | 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 | a0001c0001t0038g0064a0001c0001t0072g0174a0001c0001t0073g0046others(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 | 28 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(25): 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 | 36 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(33): 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 | 3 | a0001c0001t0007g0120a0001c0001t0066g0116a0001c0001t0070g0121 | 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 | a0001c0001t0002g0025a0001c0001t0003g0042a0001c0001t0003g0052others(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
|
GA | G | 3 | a0001c0001t0090g0094a0001c0001t0098g0181a0001c0001t0100g0018 | 3 | NA18942.hp1 NA18953.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.403-11565delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647219 | ||||||
| chrX:138647219
|
GAAAAAAA others(3): Show |
G | 8 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0001g0005 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0093g0123others(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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0093g0123others(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:138647736
|
CTAAG | C | 1 | a0001c0001t0037g0020 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.403-12085_403-1208 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647736 | ||||||
| chrX:138647831
|
C | CA | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-12177dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138647831 | ||||||
| chrX:138648042
|
C | CA | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-12388dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648042 | ||||||
| chrX:138648053
|
A | T | 5 | a0001c0001t0008g0001a0001c0001t0008g0030a0001c0001t0008g0043others(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:138648059
|
T | TA | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-12405dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648059 | ||||||
| chrX:138648344
|
T | TA | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-12690dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648344 | ||||||
| chrX:138648365
|
G | C | 1 | a0001c0001t0092g0168 | 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 | a0001c0001t0061g0068 | 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 | a0001c0001t0036g0191 | 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 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0122g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403-13093C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648748 | ||||||
| chrX:138648813
|
C | CA | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-13159dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648813 | ||||||
| chrX:138648817
|
C | T | 1 | a0001c0001t0004g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-13162G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648817 | ||||||
| chrX:138648970
|
A | AT | 1 | a0001c0001t0013g0038 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403-13316dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138648970 | ||||||
| chrX:138649056
|
C | G | 2 | a0001c0001t0102g0031a0001c0001t0103g0028 | 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 | 192 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 209 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0011g0163 | 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 | a0001c0001t0104g0185 | 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 | a0001c0001t0090g0094 | 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 | a0001c0001t0077g0058 | 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 | a0001c0001t0025g0179 | 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 | a0001c0001t0109g0065 | 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 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0007g0110 | 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 | a0001c0001t0025g0183a0001c0001t0100g0018a0001c0001t0101g0184 | 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 | a0001c0001t0006g0002a0001c0001t0006g0007a0001c0001t0006g0067others(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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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:138650588
|
AT | A | 1 | a0001c0001t0036g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403-14934delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138650588 | ||||||
| chrX:138650766
|
A | C | 8 | a0001c0001t0024g0014a0001c0001t0093g0123a0001c0001t0094g0196others(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 | a0001c0001t0013g0037 | 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 | a0001c0001t0041g0197a0001c0001t0084g0193a0001c0001t0113g0192 | 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 | a0001c0001t0041g0197 | 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 | a0001c0001t0076g0133a0001c0001t0085g0130 | 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 | a0001c0001t0050g0164 | 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 | a0001c0001t0028g0016a0001c0001t0030g0158 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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 | a0001c0001t0104g0185 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0094g0196others(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 | a0001c0001t0007g0125 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0010g0122 | 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 | a0001c0001t0103g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.403-18201G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653856 | ||||||
| chrX:138653868
|
AT | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403-18214delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138653868 | ||||||
| chrX:138654031
|
G | GT | 1 | a0001c0001t0046g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.403-18377dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654031 | ||||||
| chrX:138654059
|
T | C | 3 | a0001c0001t0041g0197a0001c0001t0084g0193a0001c0001t0113g0192 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0094g0196others(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 | 6 | a0001c0001t0004g0015a0001c0001t0004g0207a0001c0001t0004g0210others(3): Show | 7 | HG00438.hp2 HG02071.hp1 NA18954.hp2 others(4): 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 | a0001c0001t0041g0197a0001c0001t0084g0193a0001c0001t0113g0192 | 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 | a0001c0001t0044g0177a0001c0001t0102g0031a0001c0001t0103g0028others(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 | a0001c0001t0005g0105 | 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 | 21 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(18): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.403-19001C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654656 | ||||||
| chrX:138654744
|
A | AATAC | 80 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(77): Show | 86 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(83): 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 |
27 | a0001c0001t0004g0202a0001c0001t0005g0069a0001c0001t0005g0071others(24): 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 | a0001c0001t0020g0093 | 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 | a0001c0001t0007g0108a0001c0001t0024g0014a0001c0001t0036g0191others(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:138654768
|
C | CATAT | 1 | a0001c0001t0004g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.403-19114_403-1911 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138654768 | ||||||
| chrX:138654794
|
G | A | 2 | a0001c0001t0041g0197a0001c0001t0113g0192 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0036g0191 | 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 | a0001c0001t0044g0177a0001c0001t0102g0031a0001c0001t0103g0028 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0061g0068 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0104g0185 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | a0001c0001t0045g0118a0001c0001t0069g0119 | 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 | 2 | a0001c0001t0012g0004a0001c0001t0031g0175 | 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 | a0001c0001t0025g0183 | 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 | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(78): 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 | 121 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(118): Show | 128 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(125): 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 | a0001c0001t0040g0112 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | a0001c0001t0024g0014 | 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 | a0001c0001t0005g0069a0001c0001t0018g0126 | 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:138657157
|
T | TA | 1 | a0001c0001t0075g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.403-21503dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138657157 | ||||||
| chrX:138657158
|
A | T | 1 | a0001c0001t0005g0075 | 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 | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(78): 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 | a0001c0001t0077g0058 | 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 | a0001c0001t0007g0108 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0003g0052a0001c0001t0043g0054 | 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 | 21 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(18): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0003g0041 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0099g0140 | 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 | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(78): 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138660040
|
C | CA | 218 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.403-24386_403-2438 others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138660040 | ||||||
| chrX:138660084
|
T | A | 22 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(19): Show | 23 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(20): 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0036g0191a0001c0001t0113g0192 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | 7 | a0001c0001t0001g0011a0001c0001t0001g0144a0001c0001t0001g0148others(4): 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 | a0001c0001t0064g0036 | 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 | a0001c0001t0099g0140 | 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 | a0001c0001t0099g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-25692G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661347 | ||||||
| chrX:138661583
|
TTC | T | 2 | a0001c0001t0005g0069a0001c0001t0047g0170 | 2 | HG00673.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.403-25930_403-2592 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138661583 | ||||||
| chrX:138661652
|
A | G | 3 | a0001c0001t0017g0060a0001c0001t0017g0142a0001c0001t0054g0143 | 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 | a0001c0001t0129g0204 | 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 | a0001c0001t0099g0140 | 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 | 22 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(19): Show | 23 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(20): 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 | a0001c0001t0007g0108a0001c0001t0086g0109 | 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 | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(82): 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:138664558
|
T | TGAGAGA | 1 | a0001c0001t0061g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-28909_403-2890 others(10): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138664558 | ||||||
| chrX:138664560
|
A | T | 1 | a0001c0001t0083g0032 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0038g0064 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | 15 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0006g0002others(12): 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:138666256
|
TGA | T | 1 | a0001c0001t0002g0086 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.403-30603_403-3060 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138666256 | ||||||
| chrX:138666548
|
C | T | 12 | a0001c0001t0007g0083a0001c0001t0007g0108a0001c0001t0007g0110others(9): 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0045g0118a0001c0001t0069g0119 | 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 | a0001c0001t0106g0187 | 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 | a0001c0001t0106g0187 | 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 | 22 | a0001c0001t0004g0015a0001c0001t0004g0202a0001c0001t0004g0207others(19): Show | 23 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.403-31617A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667272 | ||||||
| chrX:138667274
|
G | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(29): 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0028g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.403-32205C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667860 | ||||||
| chrX:138667999
|
TA | T | 1 | a0001c0001t0006g0159 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.403-32345delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138667999 | ||||||
| chrX:138668040
|
T | C | 1 | a0001c0001t0061g0068 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138668319
|
TC | T | 1 | a0001c0001t0064g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.403-32665delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138668319 | ||||||
| chrX:138668432
|
T | C | 1 | a0001c0001t0009g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.403-32777A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138668432 | ||||||
| chrX:138669340
|
G | GA | 2 | a0001c0001t0103g0028a0001c0001t0104g0185 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.402+33643dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138669340 | ||||||
| chrX:138669544
|
CT | C | 1 | a0001c0001t0064g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.402+33439delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138669544 | ||||||
| chrX:138669592
|
T | C | 3 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190 | 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 | a0001c0001t0071g0073 | 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 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0053g0074 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | 15 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0006g0002others(12): 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 | 125 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(122): Show | 132 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(129): 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0003g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.402+31621A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671363 | ||||||
| chrX:138671398
|
TC | T | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+31585delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671398 | ||||||
| chrX:138671499
|
A | T | 1 | a0001c0001t0044g0177 | 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 | a0001c0001t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.402+31377A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671607 | ||||||
| chrX:138671630
|
CA | C | 1 | a0001c0001t0037g0020 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.402+31353delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671630 | ||||||
| chrX:138671693
|
C | T | 4 | a0001c0001t0003g0006a0001c0001t0003g0059a0001c0001t0065g0055others(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 | a0001c0001t0062g0082 | 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 | 86 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(83): 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 | a0001c0001t0004g0200a0001c0001t0004g0201 | 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:138671974
|
TG | T | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+31009delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138671974 | ||||||
| chrX:138672020
|
TA | T | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30963delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672020 | ||||||
| chrX:138672065
|
A | T | 8 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138672184
|
AT | A | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30799delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672184 | ||||||
| chrX:138672268
|
G | A | 104 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(101): Show | 110 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.402+30716C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672268 | ||||||
| chrX:138672375
|
GA | G | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30608delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672375 | ||||||
| chrX:138672421
|
C | T | 4 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138672435
|
T | TG | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30548dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672435 | ||||||
| chrX:138672499
|
G | GC | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30484dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672499 | ||||||
| chrX:138672521
|
C | T | 4 | a0001c0001t0003g0006a0001c0001t0003g0059a0001c0001t0065g0055others(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:138672576
|
A | AT | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30407dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672576 | ||||||
| chrX:138672586
|
TTG | T | 1 | a0001c0001t0019g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+30396_402+3039 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138672586 | ||||||
| chrX:138672687
|
G | A | 1 | a0001c0001t0083g0032 | 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 | a0001c0001t0045g0118 | 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 | a0001c0001t0105g0188 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 | a0001c0001t0094g0196a0001c0001t0095g0195a0001c0001t0096g0194 | 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 | a0001c0001t0110g0189 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | a0001c0001t0009g0085 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0003g0029 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.402+27403A>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138675581 | ||||||
| chrX:138675793
|
C | CT | 1 | a0001c0001t0003g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.402+27190dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138675793 | ||||||
| chrX:138676577
|
G | A | 1 | a0001c0001t0099g0140 | 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 | a0001c0001t0028g0016a0001c0001t0030g0158 | 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 | a0001c0001t0002g0088a0001c0001t0021g0089 | 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 | a0001c0001t0072g0174 | 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 | a0001c0001t0056g0019 | 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 | a0001c0001t0062g0082 | 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 | a0001c0001t0014g0092 | 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 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0218others(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 | a0001c0001t0097g0146 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138678229
|
AGTGGGGA others(2): Show |
A | 1 | a0001c0001t0096g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.402+24746_402+2475 others(13): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678229 | ||||||
| chrX:138678420
|
CA | C | 1 | a0001c0001t0064g0036 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.402+24563delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138678420 | ||||||
| chrX:138678541
|
T | C | 1 | a0001c0001t0103g0028 | 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 | a0001c0001t0002g0025 | 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 | 21 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(18): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): 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 | a0001c0001t0097g0146 | 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 | a0001c0001t0106g0187 | 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 | a0001c0001t0011g0171 | 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 | a0001c0001t0127g0209a0001c0001t0128g0212 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0003g0063 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0063g0062 | 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 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0009g0106 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0003g0021 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | a0001c0001t0003g0029 | 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 | 17 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0002g0025others(14): 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 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0007g0125others(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 | a0001c0001t0107g0190 | 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 | a0001c0001t0011g0044 | 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 | 79 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(76): 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 | a0001c0001t0004g0015 | 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 | a0001c0001t0014g0092 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | a0001c0001t0075g0091 | 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 | a0001c0001t0004g0218 | 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 | a0001c0001t0073g0046 | 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 | a0001c0001t0094g0196 | 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 | a0001c0001t0016g0090a0001c0001t0024g0014a0001c0001t0036g0191others(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:138683415
|
T | TCACA | 1 | a0001c0001t0017g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.402+19565_402+1956 others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138683415 | ||||||
| chrX:138683417
|
A | T | 2 | a0001c0001t0035g0157a0001c0001t0066g0116 | 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 | a0001c0001t0044g0177a0001c0001t0102g0031a0001c0001t0103g0028others(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 | a0001c0001t0003g0053 | 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 | 23 | a0001c0001t0002g0009a0001c0001t0002g0077a0001c0001t0002g0096others(20): 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | a0001c0001t0003g0052a0001c0001t0043g0054 | 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 | a0001c0001t0004g0200a0001c0001t0004g0201 | 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 | a0001c0001t0125g0203 | 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 | 123 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(120): Show | 130 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(127): 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 | a0001c0001t0023g0098 | 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 | a0001c0001t0004g0210 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.402+15741G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687243 | ||||||
| chrX:138687400
|
AAT | A | 1 | a0001c0001t0106g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402+15582_402+1558 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687400 | ||||||
| chrX:138687731
|
C | T | 1 | a0001c0001t0004g0200 | 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 | a0001c0001t0004g0015 | 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 | a0001c0001t0058g0114 | 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 | 8 | a0001c0001t0001g0156a0001c0001t0003g0052a0001c0001t0003g0053others(5): 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:138687953
|
A | ATT | 1 | a0001c0001t0099g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+15029_402+1503 others(6): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687953 | ||||||
| chrX:138687953
|
AT | A | 3 | a0001c0001t0003g0063a0001c0001t0090g0094a0001c0001t0122g0211 | 3 | HG02451.hp1 NA18953.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.402+15030delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138687953 | ||||||
| chrX:138687992
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0186 | 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 | a0001c0001t0010g0127a0001c0001t0058g0114a0001c0001t0093g0123 | 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:138688131
|
AT | A | 1 | a0001c0001t0090g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.402+14852delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688131 | ||||||
| chrX:138688446
|
A | G | 1 | a0001c0001t0044g0177 | 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 | 187 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(184): Show | 204 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.402+14376G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688608 | ||||||
| chrX:138688625
|
T | TA | 1 | a0001c0001t0046g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.402+14358dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138688625 | ||||||
| chrX:138688835
|
C | T | 8 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | a0001c0001t0004g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+13628A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138689356 | ||||||
| chrX:138689412
|
G | GC | 218 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.402+13571dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138689412 | ||||||
| chrX:138689488
|
G | A | 8 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0014g0154 | 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 | 84 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(81): 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:138690520
|
CT | C | 1 | a0001c0001t0090g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.402+12463delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138690520 | ||||||
| chrX:138691023
|
T | C | 1 | a0001c0001t0041g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+11961A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691023 | ||||||
| chrX:138691101
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+11882dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691101 | ||||||
| chrX:138691134
|
C | A | 1 | a0001c0001t0128g0212 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | 79 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(76): 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 | a0001c0001t0002g0077a0001c0001t0002g0096a0001c0001t0002g0097others(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 | a0001c0001t0066g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.402+11362G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691622 | ||||||
| chrX:138691776
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+11207dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138691776 | ||||||
| chrX:138691925
|
C | A | 8 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | 21 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(18): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.402+10939A>C | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692045 | ||||||
| chrX:138692387
|
G | GT | 4 | a0001c0001t0001g0178a0001c0001t0004g0201a0001c0001t0004g0218others(1): Show | 4 | HG02647.hp1 HG03516.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+10596dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692387 | ||||||
| chrX:138692387
|
GT | G | 3 | a0001c0001t0041g0197a0001c0001t0054g0143a0001c0001t0118g0198 | 3 | HG02074.hp1 HG02622.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.402+10596delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692387 | ||||||
| chrX:138692401
|
T | C | 4 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138692620
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+10363dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692620 | ||||||
| chrX:138692642
|
C | T | 1 | a0001c0001t0041g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+10342G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692642 | ||||||
| chrX:138692694
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+10289dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692694 | ||||||
| chrX:138692720
|
A | ATG | 5 | a0001c0001t0008g0001a0001c0001t0008g0030a0001c0001t0008g0043others(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 | a0001c0001t0024g0014 | 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:138692909
|
A | AT | 3 | a0001c0001t0001g0172a0001c0001t0016g0095a0001c0001t0051g0153 | 3 | HG01516.hp2 HG03942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.402+10074dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138692909 | ||||||
| chrX:138693324
|
T | A | 8 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0099g0140 | 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 | a0001c0001t0018g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+8624C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694360 | ||||||
| chrX:138694434
|
C | CTT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8548_402+8549d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694434 | ||||||
| chrX:138694450
|
T | TA | 3 | a0001c0001t0094g0196a0001c0001t0095g0195a0001c0001t0096g0194 | 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 | a0001c0001t0024g0014 | 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 | a0001c0001t0094g0196a0001c0001t0095g0195a0001c0001t0096g0194 | 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:138694451
|
CT | C | 3 | a0001c0001t0033g0076a0001c0001t0100g0018a0001c0001t0109g0065 | 3 | NA18951.hp1 NA18951.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.402+8532delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694451 | ||||||
| chrX:138694454
|
T | TTC | 1 | a0001c0001t0029g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.402+8529_402+8530i others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694454 | ||||||
| chrX:138694537
|
G | A | 2 | a0001c0001t0009g0081a0001c0001t0009g0115 | 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:138694569
|
G | GC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8414dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694569 | ||||||
| chrX:138694617
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8366dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694617 | ||||||
| chrX:138694638
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8345dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694638 | ||||||
| chrX:138694732
|
TC | T | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8251delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694732 | ||||||
| chrX:138694763
|
C | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.402+8221G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694763 | ||||||
| chrX:138694764
|
A | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 239 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.402+8220T>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694764 | ||||||
| chrX:138694917
|
A | AC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+8066dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694917 | ||||||
| chrX:138694984
|
GAAA | G | 1 | a0001c0001t0005g0149 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.402+7997_402+7999d others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694984 | ||||||
| chrX:138694985
|
AAAC | A | 1 | a0001c0001t0089g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.402+7996_402+7998d others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694985 | ||||||
| chrX:138694986
|
A | AAC | 18 | a0001c0001t0003g0029a0001c0001t0005g0075a0001c0001t0008g0043others(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 | 27 | a0001c0001t0002g0008a0001c0001t0002g0025a0001c0001t0002g0086others(24): 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
|
A | AACACAC | 1 | a0001c0001t0060g0070 | 1 | HG01496.hp2 | 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
|
A | AC | 1 | a0001c0001t0016g0090 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.402+7997_402+7998i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | ||||||
| chrX:138694986
|
A | ACAC | 1 | a0001c0001t0001g0150 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.402+7997_402+7998i others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138694986 | ||||||
| chrX:138694986
|
AAC | A | 28 | a0001c0001t0003g0061a0001c0001t0004g0202a0001c0001t0005g0079others(25): 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 | a0001c0001t0002g0124a0001c0001t0004g0200a0001c0001t0004g0213others(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 | 26 | a0001c0001t0001g0178a0001c0001t0004g0015a0001c0001t0004g0201others(23): Show | 27 | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(24): 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 | 35 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(32): 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 | a0001c0001t0103g0028 | 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 | a0001c0001t0007g0125a0001c0001t0018g0126 | 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 | a0001c0001t0104g0185 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138695032
|
CA | C | 1 | a0001c0001t0062g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.402+7951delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695032 | ||||||
| chrX:138695033
|
A | AC | 1 | a0001c0001t0085g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.402+7950_402+7951i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695033 | ||||||
| chrX:138695033
|
A | ACAC | 1 | a0001c0001t0117g0034 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.402+7950_402+7951i others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695033 | ||||||
| chrX:138695033
|
A | ACACAC | 3 | a0001c0001t0005g0069a0001c0001t0021g0084a0001c0001t0057g0033 | 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:138695033
|
AAAC | A | 1 | a0001c0001t0011g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.402+7948_402+7950d others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695033 | ||||||
| chrX:138695110
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+7873dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695110 | ||||||
| chrX:138695363
|
C | T | 4 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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:138695422
|
T | TA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+7561dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138695422 | ||||||
| chrX:138696121
|
A | C | 3 | a0001c0001t0007g0083a0001c0001t0007g0134a0001c0001t0062g0082 | 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 | a0001c0001t0003g0061 | 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 | a0001c0001t0044g0177a0001c0001t0102g0031a0001c0001t0103g0028 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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:138696659
|
G | GT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+6324dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696659 | ||||||
| chrX:138696796
|
C | T | 1 | a0001c0001t0103g0028 | 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 | a0001c0001t0009g0081 | 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:138696946
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+6037dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696946 | ||||||
| chrX:138696961
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+6022dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696961 | ||||||
| chrX:138696967
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+6016dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696967 | ||||||
| chrX:138696991
|
A | AAC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5991_402+5992d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696991 | ||||||
| chrX:138696997
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5986_402+5987i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138696997 | ||||||
| chrX:138697004
|
A | AC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5979_402+5980i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697004 | ||||||
| chrX:138697121
|
TA | T | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5862delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697121 | ||||||
| chrX:138697159
|
A | AGT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5823_402+5824d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697159 | ||||||
| chrX:138697177
|
C | CA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5806dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697177 | ||||||
| chrX:138697359
|
A | AGT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5623_402+5624d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697359 | ||||||
| chrX:138697377
|
A | ACTG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5604_402+5606d others(5): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697377 | ||||||
| chrX:138697443
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5540dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697443 | ||||||
| chrX:138697471
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5512_402+5513i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697471 | ||||||
| chrX:138697489
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5494_402+5495i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697489 | ||||||
| chrX:138697495
|
C | A | 1 | a0001c0001t0041g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+5489G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697495 | ||||||
| chrX:138697564
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5419dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697564 | ||||||
| chrX:138697627
|
G | GT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5356dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697627 | ||||||
| chrX:138697633
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5350_402+5351i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697633 | ||||||
| chrX:138697646
|
A | T | 12 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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:138697718
|
A | AAT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5265_402+5266i others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697718 | ||||||
| chrX:138697736
|
T | TG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5247dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697736 | ||||||
| chrX:138697784
|
C | CT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5199dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697784 | ||||||
| chrX:138697820
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5163_402+5164i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697820 | ||||||
| chrX:138697859
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5124dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697859 | ||||||
| chrX:138697879
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5104dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697879 | ||||||
| chrX:138697939
|
CA | C | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+5044delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697939 | ||||||
| chrX:138697992
|
C | CA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4991dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138697992 | ||||||
| chrX:138698029
|
C | CAT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4954_402+4955i others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698029 | ||||||
| chrX:138698061
|
C | CA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4922dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698061 | ||||||
| chrX:138698082
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0052g0147 | 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:138698134
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4849dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698134 | ||||||
| chrX:138698164
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.402+4820C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698164 | ||||||
| chrX:138698186
|
A | AG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4797dupC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698186 | ||||||
| chrX:138698216
|
T | C | 1 | a0001c0001t0074g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.402+4768A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698216 | ||||||
| chrX:138698244
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4739dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698244 | ||||||
| chrX:138698284
|
T | C | 5 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0218others(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:138698330
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4653_402+4654i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698330 | ||||||
| chrX:138698334
|
T | TACTAG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4649_402+4650i others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698334 | ||||||
| chrX:138698340
|
A | T | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4644T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698340 | ||||||
| chrX:138698353
|
A | AAG | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4629_402+4630d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698353 | ||||||
| chrX:138698369
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4614dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698369 | ||||||
| chrX:138698377
|
GATAAA | G | 1 | a0001c0001t0003g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.402+4602_402+4606d others(7): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698377 | ||||||
| chrX:138698402
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4581dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698402 | ||||||
| chrX:138698419
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4564dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698419 | ||||||
| chrX:138698471
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4512dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698471 | ||||||
| chrX:138698632
|
G | A | 1 | a0001c0001t0112g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.402+4352C>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698632 | ||||||
| chrX:138698632
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4351dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698632 | ||||||
| chrX:138698643
|
T | TA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4340_402+4341i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698643 | ||||||
| chrX:138698648
|
A | AC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4335_402+4336i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698648 | ||||||
| chrX:138698702
|
A | AT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4281_402+4282i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698702 | ||||||
| chrX:138698809
|
G | GT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+4174dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138698809 | ||||||
| chrX:138699032
|
C | CA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3951dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699032 | ||||||
| chrX:138699066
|
T | G | 1 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3915G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699069 | ||||||
| chrX:138699118
|
G | GA | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3865dupT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699118 | ||||||
| chrX:138699124
|
T | C | 1 | a0001c0001t0074g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.402+3860A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699124 | ||||||
| chrX:138699184
|
AC | A | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3799delG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699184 | ||||||
| chrX:138699277
|
TA | T | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3706delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699277 | ||||||
| chrX:138699476
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3507dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699476 | ||||||
| chrX:138699625
|
C | A | 8 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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:138699626
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3357dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699626 | ||||||
| chrX:138699631
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3352_402+3353i others(3): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699631 | ||||||
| chrX:138699695
|
C | T | 1 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0036g0191a0001c0001t0041g0197a0001c0001t0084g0193others(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 | a0001c0001t0002g0129 | 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 | a0001c0001t0049g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.402+3140G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699844 | ||||||
| chrX:138699921
|
T | TC | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+3062dupG | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138699921 | ||||||
| chrX:138700014
|
G | GT | 1 | a0001c0001t0009g0081 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.402+2969dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138700014 | ||||||
| chrX:138700388
|
G | A | 1 | a0001c0001t0102g0031 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 | a0001c0001t0006g0067 | 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 | 21 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(18): Show | 22 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(19): 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 | a0001c0001t0001g0172 | 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 | 20 | a0001c0001t0004g0015a0001c0001t0004g0200a0001c0001t0004g0201others(17): Show | 21 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(18): 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 | a0001c0001t0044g0177 | 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 | a0001c0001t0063g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.402+1805A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701179 | ||||||
| chrX:138701214
|
T | C | 1 | a0001c0001t0121g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.402+1770A>G | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138701214 | ||||||
| chrX:138701321
|
C | G | 1 | a0001c0001t0099g0140 | 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 | a0001c0001t0006g0002a0001c0001t0006g0007a0001c0001t0006g0067others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0083g0032 | 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 | a0001c0001t0044g0177a0001c0001t0097g0146a0001c0001t0103g0028 | 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 | 92 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 99 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.402+789T>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702195 | ||||||
| chrX:138702195
|
AAATTAAT others(1): Show |
A | 1 | a0001c0001t0007g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.402+781_402+788del others(8): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702195 | ||||||
| chrX:138702199
|
T | A | 11 | a0001c0001t0003g0063a0001c0001t0038g0064a0001c0001t0039g0131others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | 4 | a0001c0001t0078g0139a0001c0001t0079g0136a0001c0001t0080g0137others(1): Show | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0006g0002a0001c0001t0006g0007a0001c0001t0006g0067others(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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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 | a0001c0001t0018g0138 | 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 | a0001c0001t0024g0014a0001c0001t0094g0196a0001c0001t0095g0195others(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:138702616
|
G | GT | 1 | a0001c0001t0004g0015 | 2 | NA18954.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.402+367dupA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 3/4 | chrX | 138702616 | ||||||
| chrX:138702778
|
A | T | 1 | a0001c0001t0114g0027 | 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 | a0001c0001t0111g0026 | 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 | a0001c0001t0001g0144a0001c0001t0022g0145 | 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:138703280
|
CAGAT | C | 1 | a0001c0001t0078g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.299-197_299-194del others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138703280 | ||||||
| chrX:138704362
|
T | C | 1 | a0001c0001t0041g0197 | 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 | a0001c0001t0004g0200a0001c0001t0004g0201 | 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 | a0001c0001t0017g0142a0001c0001t0054g0143a0001c0001t0089g0141 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 | a0001c0001t0061g0068 | 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 | a0001c0001t0105g0188a0001c0001t0106g0187a0001c0001t0107g0190others(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 | 101 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0025others(98): Show | 107 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.298+2631delC | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706186 | ||||||
| chrX:138706274
|
T | C | 1 | a0001c0001t0099g0140 | 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 | a0001c0001t0002g0025a0002c0002t0108g0024 | 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 | a0001c0001t0104g0185 | 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 | a0001c0001t0059g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+1907G>A | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138706911 | ||||||
| chrX:138707169
|
G | GGT | 1 | a0001c0001t0059g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298+1647_298+1648d others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707169 | ||||||
| chrX:138707267
|
CT | C | 1 | a0001c0001t0002g0173 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.298+1550delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138707267 | ||||||
| chrX:138707268
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(39): 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 | 11 | a0001c0001t0003g0021a0001c0001t0025g0179a0001c0001t0025g0183others(8): 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 | a0001c0001t0072g0174 | 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 | 2 | a0001c0001t0012g0004a0001c0001t0031g0175 | 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 | a0001c0001t0049g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+461G>T | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138708357 | ||||||
| chrX:138708644
|
TAGAC | T | 1 | a0001c0001t0106g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.298+170_298+173del others(4): Show |
FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 2/4 | chrX | 138708644 | ||||||
| chrX:138708968
|
T | C | 1 | a0001c0001t0044g0177 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0005 | 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 | 7 | a0001c0001t0025g0179a0001c0001t0025g0183a0001c0001t0026g0180others(4): 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:138710218
|
CT | C | 1 | a0001c0001t0104g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+598delA | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710218 | ||||||
| chrX:138710233
|
CA | C | 1 | a0001c0001t0100g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.187+583delT | FGF13 | ENSG00000129682.16 | transcript | ENST00000315930.11 | protein_coding | 1/4 | chrX | 138710233 | ||||||
| chrX:138710404
|
A | T | 1 | a0001c0001t0074g0017 | 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 | a0001c0001t0004g0218a0001c0001t0004g0219 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0024g0014a0001c0001t0036g0191a0001c0001t0041g0197others(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 |