| geneid | 2259 |
|---|---|
| ensemblid | ENSG00000102466.17 |
| hgncid | 3671 |
| symbol | FGF14 |
| name | fibroblast growth factor 14 |
| refseq_nuc | NM_004115.4 |
| refseq_prot | NP_004106.1 |
| ensembl_nuc | ENST00000376143.5 |
| ensembl_prot | ENSP00000365313.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 101710804 |
| end | 101916945 |
| strand | - |
| ver | v1.2 |
| region | chr13:101710804-101916945 |
| region5000 | chr13:101705804-101921945 |
| regionname0 | FGF14_chr13_101710804_101916945 |
| regionname5000 | FGF14_chr13_101705804_101921945 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 247 | 266 | 88 | 50 | 82 | 10 | 34 | 56 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 744 | 261 | 84 | 49 | 82 | 10 | 34 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| c0002 | 0/0 | 744 | 5 | 4 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 12330 | 9 | 1 | 2 | 3 | 1 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0002 | 0/0 | 12323 | 7 | 0 | 0 | 6 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0003 | 0/0 | 12332 | 6 | 0 | 2 | 2 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0004 | 0/0 | 12327 | 6 | 0 | 5 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0005 | 0/0 | 12335 | 5 | 0 | 0 | 5 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0006 | 0/0 | 12325 | 5 | 0 | 1 | 1 | 2 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0007 | 0/0 | 12329 | 5 | 0 | 3 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0008 | 0/0 | 12330 | 5 | 1 | 2 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0009 | 0/0 | 12329 | 5 | 2 | 1 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0010 | 0/0 | 12332 | 4 | 0 | 1 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0011 | 0/0 | 12323 | 4 | 1 | 1 | 1 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0012 | 0/0 | 12325 | 4 | 0 | 0 | 3 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0013 | 0/0 | 12347 | 4 | 3 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0014 | 0/0 | 12317 | 3 | 2 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0015 | 0/0 | 12325 | 3 | 1 | 0 | 0 | 1 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0016 | 0/0 | 12334 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0017 | 0/0 | 12325 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0018 | 0/0 | 12332 | 3 | 0 | 0 | 2 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0019 | 0/0 | 12343 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0020 | 0/0 | 12325 | 3 | 0 | 0 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0021 | 0/0 | 12327 | 3 | 1 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0022 | 0/0 | 12322 | 3 | 0 | 0 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0023 | 0/0 | 12334 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0024 | 0/0 | 12320 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0025 | 0/0 | 12330 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0026 | 0/0 | 12333 | 2 | 0 | 2 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0027 | 0/0 | 12333 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0028 | 0/0 | 12338 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0029 | 0/0 | 12334 | 2 | 1 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0030 | 0/0 | 12332 | 2 | 0 | 0 | 1 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0031 | 0/0 | 12338 | 2 | 0 | 1 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0032 | 0/0 | 12336 | 2 | 0 | 2 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0033 | 0/0 | 12334 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0034 | 0/0 | 12325 | 2 | 0 | 1 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0035 | 0/0 | 12320 | 2 | 1 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0036 | 0/0 | 12323 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0037 | 0/0 | 12333 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0038 | 0/0 | 12330 | 2 | 0 | 0 | 0 | 1 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0039 | 0/0 | 12325 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0040 | 0/0 | 12333 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0041 | 0/0 | 12334 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0042 | 0/0 | 12335 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0043 | 0/0 | 12332 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0044 | 0/0 | 12328 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0045 | 0/0 | 12320 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0046 | 0/0 | 12321 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0047 | 0/0 | 12331 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0048 | 0/0 | 12323 | 2 | 1 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0049 | 0/0 | 12327 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0050 | 0/0 | 12325 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0051 | 0/0 | 12331 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0052 | 0/0 | 12332 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0053 | 0/0 | 12325 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0054 | 0/0 | 12339 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0055 | 0/0 | 12325 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0056 | 0/0 | 12325 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0057 | 0/0 | 12326 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0058 | 0/0 | 12334 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0059 | 0/1 | 12337 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0060 | 0/0 | 12333 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0061 | 0/0 | 12331 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0062 | 0/0 | 12329 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0063 | 0/0 | 12329 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0064 | 0/0 | 12325 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0065 | 0/0 | 12325 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0066 | 0/0 | 12338 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0067 | 0/0 | 12330 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0068 | 0/0 | 12342 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0069 | 0/0 | 12340 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0070 | 0/0 | 12334 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0071 | 0/0 | 12334 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0072 | 0/0 | 12332 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0073 | 0/0 | 12331 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0074 | 0/0 | 12331 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0075 | 0/0 | 12332 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0076 | 0/0 | 12332 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0077 | 0/0 | 12334 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0078 | 0/0 | 12332 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0079 | 0/0 | 12321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0080 | 0/0 | 12347 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0081 | 0/0 | 12345 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0082 | 0/0 | 12341 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0083 | 0/0 | 12343 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0084 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0085 | 0/0 | 12325 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0086 | 0/0 | 12321 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0087 | 0/0 | 12332 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0088 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0089 | 0/0 | 12327 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0090 | 0/0 | 12324 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0091 | 0/0 | 12347 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0092 | 0/0 | 12330 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0093 | 0/0 | 12325 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0094 | 0/0 | 12349 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0095 | 0/0 | 12335 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0096 | 0/0 | 12346 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0097 | 0/0 | 12344 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0098 | 0/0 | 12342 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0099 | 0/0 | 12340 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0100 | 0/0 | 12321 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0101 | 0/0 | 12323 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0102 | 0/0 | 12343 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0103 | 0/0 | 12327 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0104 | 0/0 | 12334 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0105 | 0/0 | 12346 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0106 | 0/0 | 12326 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0107 | 0/0 | 12333 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0108 | 0/0 | 12333 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0109 | 0/0 | 12329 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0110 | 0/0 | 12334 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0111 | 0/0 | 12336 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0112 | 0/0 | 12337 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0113 | 0/0 | 12334 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0114 | 0/0 | 12333 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0115 | 0/0 | 12332 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0116 | 0/0 | 12332 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0117 | 0/0 | 12332 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0118 | 0/0 | 12332 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0119 | 0/0 | 12333 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0120 | 0/0 | 12332 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0121 | 0/0 | 12332 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0122 | 0/0 | 12330 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0123 | 0/0 | 12330 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0124 | 0/0 | 12328 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0125 | 0/0 | 12328 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0126 | 0/0 | 12332 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0127 | 0/0 | 12317 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0128 | 0/0 | 12317 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0129 | 0/0 | 12343 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0130 | 0/0 | 12343 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0131 | 0/0 | 12341 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0132 | 0/0 | 12336 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0133 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0134 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0135 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0136 | 0/0 | 12327 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0137 | 0/0 | 12332 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0138 | 0/0 | 12325 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0139 | 0/0 | 12323 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0140 | 0/0 | 12322 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0141 | 0/0 | 12323 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0142 | 0/0 | 12323 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0143 | 0/0 | 12320 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0144 | 0/0 | 12314 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0145 | 0/0 | 12329 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0146 | 0/0 | 12332 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0147 | 0/0 | 12331 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0148 | 0/0 | 12328 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0149 | 0/0 | 12328 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0150 | 0/0 | 12328 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0151 | 0/0 | 12338 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0152 | 0/0 | 12325 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0153 | 0/0 | 12333 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0154 | 0/0 | 12344 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0155 | 0/0 | 12325 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0156 | 0/0 | 12324 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0157 | 0/0 | 12323 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0158 | 0/0 | 12343 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0159 | 0/0 | 12343 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0160 | 0/0 | 12324 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0161 | 0/0 | 12334 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0162 | 0/0 | 12329 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| t0163 | 1/0 | 12328 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 744 | 261 | 84 | 49 | 82 | 10 | 34 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0002 | 0/0 | 744 | 5 | 4 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13073 | 9 | 1 | 2 | 3 | 1 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0002 | 0/0 | 13066 | 7 | 0 | 0 | 6 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0003 | 0/0 | 13075 | 6 | 0 | 2 | 2 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0004 | 0/0 | 13070 | 6 | 0 | 5 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0005 | 0/0 | 13078 | 5 | 0 | 0 | 5 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0006 | 0/0 | 13068 | 5 | 0 | 1 | 1 | 2 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0007 | 0/0 | 13072 | 5 | 0 | 3 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0008 | 0/0 | 13073 | 5 | 1 | 2 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0009 | 0/0 | 13072 | 5 | 2 | 1 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0010 | 0/0 | 13075 | 4 | 0 | 1 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0011 | 0/0 | 13066 | 4 | 1 | 1 | 1 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0012 | 0/0 | 13068 | 4 | 0 | 0 | 3 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0013 | 0/0 | 13090 | 4 | 3 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0015 | 0/0 | 13068 | 3 | 1 | 0 | 0 | 1 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0016 | 0/0 | 13077 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0017 | 0/0 | 13068 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0018 | 0/0 | 13075 | 3 | 0 | 0 | 2 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0019 | 0/0 | 13086 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0020 | 0/0 | 13068 | 3 | 0 | 0 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0021 | 0/0 | 13070 | 3 | 1 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0022 | 0/0 | 13065 | 3 | 0 | 0 | 3 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0023 | 0/0 | 13077 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0024 | 0/0 | 13063 | 3 | 3 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0025 | 0/0 | 13073 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0026 | 0/0 | 13076 | 2 | 0 | 2 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0027 | 0/0 | 13076 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0028 | 0/0 | 13081 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0029 | 0/0 | 13077 | 2 | 1 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0030 | 0/0 | 13075 | 2 | 0 | 0 | 1 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0031 | 0/0 | 13081 | 2 | 0 | 1 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0032 | 0/0 | 13079 | 2 | 0 | 2 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0033 | 0/0 | 13077 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0034 | 0/0 | 13068 | 2 | 0 | 1 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0035 | 0/0 | 13063 | 2 | 1 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0036 | 0/0 | 13066 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0037 | 0/0 | 13076 | 2 | 0 | 0 | 0 | 0 | 2 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0038 | 0/0 | 13073 | 2 | 0 | 0 | 0 | 1 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0039 | 0/0 | 13068 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0040 | 0/0 | 13076 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0041 | 0/0 | 13077 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0042 | 0/0 | 13078 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0043 | 0/0 | 13075 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0044 | 0/0 | 13071 | 2 | 0 | 0 | 2 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0045 | 0/0 | 13063 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0046 | 0/0 | 13064 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0047 | 0/0 | 13074 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0048 | 0/0 | 13066 | 2 | 1 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0049 | 0/0 | 13070 | 2 | 2 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0050 | 0/0 | 13068 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0051 | 0/0 | 13074 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0052 | 0/0 | 13075 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0053 | 0/0 | 13068 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0054 | 0/0 | 13082 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0055 | 0/0 | 13068 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0056 | 0/0 | 13068 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0057 | 0/0 | 13069 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0058 | 0/0 | 13077 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0059 | 0/1 | 13080 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0060 | 0/0 | 13076 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0061 | 0/0 | 13074 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0062 | 0/0 | 13072 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0063 | 0/0 | 13072 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0064 | 0/0 | 13068 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0065 | 0/0 | 13068 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0066 | 0/0 | 13081 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0067 | 0/0 | 13073 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0068 | 0/0 | 13085 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0069 | 0/0 | 13083 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0070 | 0/0 | 13077 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0071 | 0/0 | 13077 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0072 | 0/0 | 13075 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0073 | 0/0 | 13074 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0074 | 0/0 | 13074 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0075 | 0/0 | 13075 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0076 | 0/0 | 13075 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0077 | 0/0 | 13077 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0078 | 0/0 | 13075 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0079 | 0/0 | 13064 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0080 | 0/0 | 13090 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0081 | 0/0 | 13088 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0082 | 0/0 | 13084 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0083 | 0/0 | 13086 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0084 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0085 | 0/0 | 13068 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0086 | 0/0 | 13064 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0087 | 0/0 | 13075 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0088 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0089 | 0/0 | 13070 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0090 | 0/0 | 13067 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0091 | 0/0 | 13090 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0092 | 0/0 | 13073 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0093 | 0/0 | 13068 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0094 | 0/0 | 13092 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0095 | 0/0 | 13078 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0096 | 0/0 | 13089 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0097 | 0/0 | 13087 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0098 | 0/0 | 13085 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0099 | 0/0 | 13083 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0100 | 0/0 | 13064 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0101 | 0/0 | 13066 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0102 | 0/0 | 13086 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0103 | 0/0 | 13070 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0104 | 0/0 | 13077 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0105 | 0/0 | 13089 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0106 | 0/0 | 13069 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0107 | 0/0 | 13076 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0108 | 0/0 | 13076 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0109 | 0/0 | 13072 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0110 | 0/0 | 13077 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0111 | 0/0 | 13079 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0112 | 0/0 | 13080 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0113 | 0/0 | 13077 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0114 | 0/0 | 13076 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0115 | 0/0 | 13075 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0116 | 0/0 | 13075 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0117 | 0/0 | 13075 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0118 | 0/0 | 13075 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0119 | 0/0 | 13076 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0120 | 0/0 | 13075 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0121 | 0/0 | 13075 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0122 | 0/0 | 13073 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0123 | 0/0 | 13073 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0124 | 0/0 | 13071 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0125 | 0/0 | 13071 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0126 | 0/0 | 13075 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0129 | 0/0 | 13086 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0130 | 0/0 | 13086 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0131 | 0/0 | 13084 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0132 | 0/0 | 13079 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0133 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0134 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0135 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0136 | 0/0 | 13070 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0137 | 0/0 | 13075 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0138 | 0/0 | 13068 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0139 | 0/0 | 13066 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0140 | 0/0 | 13065 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0141 | 0/0 | 13066 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0142 | 0/0 | 13066 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0143 | 0/0 | 13063 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0144 | 0/0 | 13057 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0145 | 0/0 | 13072 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0146 | 0/0 | 13075 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0147 | 0/0 | 13074 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0148 | 0/0 | 13071 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0149 | 0/0 | 13071 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0150 | 0/0 | 13071 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0151 | 0/0 | 13081 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0152 | 0/0 | 13068 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0153 | 0/0 | 13076 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0154 | 0/0 | 13087 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0155 | 0/0 | 13068 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0156 | 0/0 | 13067 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0157 | 0/0 | 13066 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0158 | 0/0 | 13086 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0159 | 0/0 | 13086 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0160 | 0/0 | 13067 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0161 | 0/0 | 13077 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0162 | 0/0 | 13072 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0001t0163 | 1/0 | 13071 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0002t0014 | 0/0 | 13060 | 3 | 2 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0002t0127 | 0/0 | 13060 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| a0001c0002t0128 | 0/0 | 13060 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | copy fasta | chr13 | 101705804 | 101921945 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0010g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0010g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0012g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0012g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0013g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0017g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0017g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0018g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0019g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0019g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0020g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0020g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0020g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0021g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0021g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0022g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0023g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0023g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0024g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0024g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0025g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0026g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0026g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0027g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0027g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0028g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0029g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0029g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0030g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0030g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0031g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0031g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0032g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0032g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0033g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0033g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0034g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0034g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0035g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0035g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0036g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0036g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0037g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0037g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0038g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0038g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0039g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0039g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0040g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0040g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0041g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0041g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0042g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0042g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0043g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0043g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0044g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0044g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0045g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0045g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0046g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0046g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0047g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0047g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0048g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0048g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0049g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0049g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0050g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0051g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0052g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0053g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0054g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0055g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0056g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0057g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0058g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0059g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0060g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0061g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0062g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0063g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0064g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0065g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0066g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0067g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0068g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0069g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0070g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0071g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0072g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0073g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0074g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0075g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0076g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0077g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0078g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0079g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0080g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0081g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0082g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0083g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0084g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0085g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0086g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0087g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0088g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0089g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0090g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0091g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0092g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0093g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0094g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0095g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0096g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0097g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0098g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0099g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0100g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0101g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0102g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0103g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0104g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0105g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0106g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0107g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0108g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0109g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0110g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0111g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0112g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0113g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0114g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0115g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0116g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0117g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0118g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0119g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0120g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0121g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0122g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0123g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0124g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0125g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0126g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0129g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0130g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0131g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0132g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0133g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0134g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0135g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0136g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0137g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0138g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0139g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0140g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0141g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0142g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0143g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0144g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0145g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0146g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0147g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0148g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0149g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0150g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0151g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0152g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0153g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0154g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0155g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0156g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0157g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0158g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0159g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0160g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0161g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0162g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0001t0163g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0002t0014g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0002t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0002t0014g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0002t0127g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| a0001c0002t0128g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0031 | g0108 | EUR | GBR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00099 | hp2 | a0001 | c0001 | t0034 | g0054 | EUR | GBR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00280 | hp1 | a0001 | c0001 | t0107 | g0175 | EUR | FIN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00280 | hp2 | a0001 | c0001 | t0063 | g0090 | EUR | FIN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0097 | EUR | FIN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00323 | hp2 | a0001 | c0001 | t0122 | g0193 | EUR | FIN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00408 | hp2 | a0001 | c0001 | t0117 | g0229 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0249 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0203 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00438 | hp1 | a0001 | c0001 | t0141 | g0197 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00438 | hp2 | a0001 | c0001 | t0052 | g0003 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00544 | hp1 | a0001 | c0001 | t0009 | g0179 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0250 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00597 | hp1 | a0001 | c0001 | t0138 | g0222 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00597 | hp2 | a0001 | c0001 | t0041 | g0226 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | CHS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00642 | hp1 | a0001 | c0001 | t0088 | g0053 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG00642 | hp2 | a0001 | c0001 | t0137 | g0240 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01074 | hp1 | a0001 | c0001 | t0087 | g0050 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0255 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0153 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01081 | hp2 | a0001 | c0001 | t0158 | g0264 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01099 | hp1 | a0001 | c0001 | t0143 | g0239 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0085 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01106 | hp1 | a0001 | c0001 | t0058 | g0068 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0152 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01109 | hp1 | a0001 | c0001 | t0086 | g0079 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0143 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0042 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0043 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01169 | hp2 | a0001 | c0001 | t0026 | g0123 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01175 | hp1 | a0001 | c0001 | t0071 | g0128 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0235 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01192 | hp1 | a0001 | c0001 | t0075 | g0092 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01192 | hp2 | a0001 | c0002 | t0014 | g0118 | AMR | PUR | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01255 | hp1 | a0001 | c0001 | t0034 | g0038 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01255 | hp2 | a0001 | c0001 | t0113 | g0234 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01256 | hp1 | a0001 | c0001 | t0026 | g0027 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01256 | hp2 | a0001 | c0001 | t0032 | g0039 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01257 | hp1 | a0001 | c0001 | t0031 | g0035 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01257 | hp2 | a0001 | c0001 | t0135 | g0183 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01258 | hp1 | a0001 | c0001 | t0084 | g0040 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01258 | hp2 | a0001 | c0001 | t0132 | g0184 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01433 | hp1 | a0001 | c0001 | t0032 | g0060 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0151 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01496 | hp2 | a0001 | c0001 | t0134 | g0180 | AMR | CLM | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0083 | EUR | IBS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01516 | hp2 | a0001 | c0001 | t0015 | g0121 | EUR | IBS | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01884 | hp1 | a0001 | c0001 | t0146 | g0156 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01884 | hp2 | a0001 | c0001 | t0081 | g0120 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01891 | hp1 | a0001 | c0001 | t0089 | g0017 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0130 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0081 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01934 | hp1 | a0001 | c0001 | t0072 | g0077 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01934 | hp2 | a0001 | c0001 | t0139 | g0181 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01943 | hp2 | a0001 | c0001 | t0136 | g0204 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01952 | hp1 | a0001 | c0001 | t0133 | g0211 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01952 | hp2 | a0001 | c0001 | t0145 | g0174 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01975 | hp2 | a0001 | c0001 | t0082 | g0072 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01978 | hp1 | a0001 | c0001 | t0056 | g0107 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01978 | hp2 | a0001 | c0001 | t0065 | g0080 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0201 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02015 | hp2 | a0001 | c0001 | t0021 | g0225 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02040 | hp1 | a0001 | c0001 | t0060 | g0100 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02040 | hp2 | a0001 | c0001 | t0070 | g0028 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02055 | hp1 | a0001 | c0001 | t0159 | g0257 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0142 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02071 | hp1 | a0001 | c0001 | t0012 | g0230 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02074 | hp1 | a0001 | c0001 | t0042 | g0205 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02074 | hp2 | a0001 | c0001 | t0033 | g0049 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02135 | hp1 | a0001 | c0001 | t0114 | g0186 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02135 | hp2 | a0001 | c0001 | t0119 | g0232 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02145 | hp1 | a0001 | c0001 | t0161 | g0263 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02145 | hp2 | a0001 | c0001 | t0150 | g0146 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02257 | hp1 | a0001 | c0001 | t0047 | g0165 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02257 | hp2 | a0001 | c0001 | t0083 | g0131 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0114 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02273 | hp2 | a0001 | c0001 | t0123 | g0198 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02280 | hp1 | a0001 | c0001 | t0153 | g0154 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0012 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02300 | hp1 | a0001 | c0001 | t0048 | g0168 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PEL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0135 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02451 | hp2 | a0001 | c0001 | t0079 | g0013 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02523 | hp1 | a0001 | c0001 | t0012 | g0216 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02572 | hp1 | a0001 | c0001 | t0106 | g0163 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0010 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02615 | hp1 | a0001 | c0001 | t0047 | g0213 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02615 | hp2 | a0001 | c0001 | t0092 | g0113 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02622 | hp1 | a0001 | c0001 | t0099 | g0011 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02622 | hp2 | a0001 | c0001 | t0090 | g0015 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02630 | hp1 | a0001 | c0001 | t0162 | g0265 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02630 | hp2 | a0001 | c0001 | t0096 | g0129 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02647 | hp1 | a0001 | c0001 | t0019 | g0247 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0260 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02698 | hp2 | a0001 | c0001 | t0120 | g0245 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02723 | hp2 | a0001 | c0001 | t0048 | g0206 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02738 | hp1 | a0001 | c0001 | t0038 | g0125 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02738 | hp2 | a0001 | c0001 | t0035 | g0044 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0115 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02809 | hp2 | a0001 | c0001 | t0023 | g0164 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02818 | hp1 | a0001 | c0001 | t0157 | g0262 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0136 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02886 | hp1 | a0001 | c0001 | t0051 | g0002 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02886 | hp2 | a0001 | c0001 | t0046 | g0148 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02895 | hp1 | a0001 | c0001 | t0023 | g0158 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02895 | hp2 | a0001 | c0001 | t0097 | g0020 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02896 | hp1 | a0001 | c0001 | t0104 | g0137 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02896 | hp2 | a0001 | c0001 | t0045 | g0215 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02897 | hp1 | a0001 | c0001 | t0045 | g0214 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02897 | hp2 | a0001 | c0001 | t0023 | g0157 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02922 | hp1 | a0001 | c0001 | t0148 | g0167 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02922 | hp2 | a0001 | c0001 | t0049 | g0218 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02965 | hp1 | a0001 | c0001 | t0102 | g0138 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02965 | hp2 | a0001 | c0002 | t0014 | g0116 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0170 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0241 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0244 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0144 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03041 | hp1 | a0001 | c0002 | t0127 | g0224 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03041 | hp2 | a0001 | c0001 | t0080 | g0021 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03098 | hp1 | a0001 | c0001 | t0154 | g0145 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03098 | hp2 | a0001 | c0001 | t0050 | g0001 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0212 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03130 | hp2 | a0001 | c0001 | t0049 | g0141 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03139 | hp1 | a0001 | c0001 | t0094 | g0119 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03195 | hp1 | a0001 | c0001 | t0093 | g0111 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03195 | hp2 | a0001 | c0001 | t0118 | g0242 | AFR | ESN | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03209 | hp1 | a0001 | c0001 | t0066 | g0112 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0139 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03225 | hp1 | a0001 | c0001 | t0131 | g0162 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03225 | hp2 | a0001 | c0001 | t0028 | g0019 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03453 | hp1 | a0001 | c0001 | t0103 | g0134 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03453 | hp2 | a0001 | c0001 | t0061 | g0025 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03490 | hp1 | a0001 | c0001 | t0036 | g0062 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03490 | hp2 | a0001 | c0001 | t0015 | g0124 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0237 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0037 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0052 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03492 | hp2 | a0001 | c0001 | t0036 | g0061 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03540 | hp1 | a0001 | c0001 | t0121 | g0160 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03540 | hp2 | a0001 | c0001 | t0160 | g0258 | AFR | GWD | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03579 | hp1 | a0001 | c0001 | t0129 | g0243 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03579 | hp2 | a0001 | c0001 | t0028 | g0018 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03654 | hp1 | a0001 | c0001 | t0027 | g0026 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03669 | hp1 | a0001 | c0001 | t0037 | g0087 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03688 | hp1 | a0001 | c0001 | t0064 | g0126 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03688 | hp2 | a0001 | c0001 | t0037 | g0066 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03704 | hp1 | a0001 | c0001 | t0027 | g0046 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03704 | hp2 | a0001 | c0001 | t0074 | g0122 | SAS | PJL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03831 | hp1 | a0001 | c0001 | t0110 | g0182 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03831 | hp2 | a0001 | c0001 | t0115 | g0176 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03834 | hp1 | a0001 | c0001 | t0076 | g0069 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0223 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03942 | hp1 | a0001 | c0001 | t0077 | g0041 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03942 | hp2 | a0001 | c0001 | t0100 | g0084 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04115 | hp1 | a0001 | c0001 | t0030 | g0023 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0059 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04184 | hp1 | a0001 | c0001 | t0062 | g0056 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04184 | hp2 | a0001 | c0001 | t0078 | g0094 | SAS | BEB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04199 | hp1 | a0001 | c0001 | t0085 | g0063 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04199 | hp2 | a0001 | c0001 | t0125 | g0238 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04204 | hp2 | a0001 | c0001 | t0116 | g0246 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG04228 | hp2 | a0001 | c0001 | t0018 | g0236 | SAS | STU | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18522 | hp1 | a0001 | c0001 | t0057 | g0086 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18522 | hp2 | a0001 | c0001 | t0130 | g0219 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | CHB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18747 | hp2 | a0001 | c0001 | t0011 | g0190 | EAS | CHB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18906 | hp1 | a0001 | c0002 | t0128 | g0155 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18906 | hp2 | a0001 | c0002 | t0014 | g0074 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18941 | hp2 | a0001 | c0001 | t0020 | g0187 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18948 | hp1 | a0001 | c0001 | t0040 | g0188 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18951 | hp1 | a0001 | c0001 | t0124 | g0251 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18951 | hp2 | a0001 | c0001 | t0073 | g0045 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0248 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18962 | hp1 | a0001 | c0001 | t0022 | g0195 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18964 | hp2 | a0001 | c0001 | t0109 | g0199 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18969 | hp2 | a0001 | c0001 | t0018 | g0221 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18970 | hp1 | a0001 | c0001 | t0144 | g0200 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18970 | hp2 | a0001 | c0001 | t0043 | g0254 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18971 | hp1 | a0001 | c0001 | t0112 | g0171 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18977 | hp1 | a0001 | c0001 | t0142 | g0228 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18977 | hp2 | a0001 | c0001 | t0039 | g0185 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18978 | hp2 | a0001 | c0001 | t0055 | g0006 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18986 | hp2 | a0001 | c0001 | t0054 | g0004 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18987 | hp1 | a0001 | c0001 | t0030 | g0032 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18987 | hp2 | a0001 | c0001 | t0111 | g0202 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18988 | hp1 | a0001 | c0001 | t0021 | g0210 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18988 | hp2 | a0001 | c0001 | t0108 | g0172 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18992 | hp1 | a0001 | c0001 | t0022 | g0194 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18992 | hp2 | a0001 | c0001 | t0033 | g0095 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18993 | hp1 | a0001 | c0001 | t0140 | g0192 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA18993 | hp2 | a0001 | c0001 | t0025 | g0007 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19000 | hp1 | a0001 | c0001 | t0039 | g0177 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19000 | hp2 | a0001 | c0001 | t0025 | g0008 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19009 | hp1 | a0001 | c0001 | t0029 | g0099 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19009 | hp2 | a0001 | c0001 | t0053 | g0005 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19043 | hp1 | a0001 | c0001 | t0156 | g0256 | AFR | LWK | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19043 | hp2 | a0001 | c0001 | t0147 | g0220 | AFR | LWK | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19054 | hp2 | a0001 | c0001 | t0152 | g0140 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0191 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19060 | hp2 | a0001 | c0001 | t0044 | g0178 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19065 | hp2 | a0001 | c0001 | t0022 | g0196 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19066 | hp1 | a0001 | c0001 | t0101 | g0105 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19066 | hp2 | a0001 | c0001 | t0069 | g0024 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19070 | hp1 | a0001 | c0001 | t0040 | g0189 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19070 | hp2 | a0001 | c0001 | t0044 | g0252 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19074 | hp1 | a0001 | c0001 | t0155 | g0149 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19074 | hp2 | a0001 | c0001 | t0041 | g0209 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19084 | hp1 | a0001 | c0001 | t0018 | g0207 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19084 | hp2 | a0001 | c0001 | t0067 | g0091 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19085 | hp1 | a0001 | c0001 | t0043 | g0253 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19090 | hp1 | a0001 | c0001 | t0042 | g0231 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19090 | hp2 | a0001 | c0001 | t0020 | g0217 | EAS | JPT | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19240 | hp1 | a0001 | c0001 | t0068 | g0009 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA19240 | hp2 | a0001 | c0001 | t0046 | g0169 | AFR | YRI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20129 | hp1 | a0001 | c0001 | t0098 | g0014 | AFR | ASW | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20129 | hp2 | a0001 | c0001 | t0035 | g0089 | AFR | ASW | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20752 | hp2 | a0001 | c0001 | t0038 | g0064 | EUR | TSI | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02109 | hp1 | a0001 | c0001 | t0151 | g0147 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02109 | hp2 | a0001 | c0001 | t0126 | g0161 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02486 | hp1 | a0001 | c0001 | t0095 | g0022 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02486 | hp2 | a0001 | c0001 | t0024 | g0259 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02559 | hp1 | a0001 | c0001 | t0105 | g0133 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | ACB | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03471 | hp1 | a0001 | c0001 | t0149 | g0166 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| HG03471 | hp2 | a0001 | c0001 | t0024 | g0261 | AFR | MSL | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0227 | AFR | USA | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| NA20300 | hp2 | a0001 | c0001 | t0091 | g0117 | AFR | USA | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0059 | g0034 | REF | REF | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0163 | g0266 | REF | REF | FGF14_chr13_101705804_101921945 | FGF14 | chr13 | 101705804 | 101921945 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:101726738
|
A | G | 1 | a0001c0002 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.481T>C | p.Leu161Leu | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/5 | 781/13071 | 481/744 | 161/247 | chr13 | 101726738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:101711096
|
G | A | 5 | a0001c0001t0016a0001c0001t0023a0001c0001t0094others(2): Show | 9 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*11735C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11735 | chr13 | 101711096 | |||||
| chr13:101711129
|
T | A | 1 | a0001c0001t0114 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11702A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11702 | chr13 | 101711129 | |||||
| chr13:101711393
|
C | A | 109 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(106): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*11438G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11438 | chr13 | 101711393 | |||||
| chr13:101711423
|
G | T | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0025others(10): Show | 28 | HG00323.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*11408C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11408 | chr13 | 101711423 | |||||
| chr13:101711450
|
G | T | 21 | a0001c0001t0013a0001c0001t0031a0001c0001t0032others(18): Show | 28 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*11381C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11381 | chr13 | 101711450 | |||||
| chr13:101711451
|
G | T | 21 | a0001c0001t0013a0001c0001t0031a0001c0001t0032others(18): Show | 28 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*11380C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 11380 | chr13 | 101711451 | |||||
| chr13:101712285
|
A | G | 1 | a0001c0001t0115 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10546T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 10546 | chr13 | 101712285 | |||||
| chr13:101712451
|
C | G | 1 | a0001c0001t0064 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10380G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 10380 | chr13 | 101712451 | |||||
| chr13:101712760
|
A | G | 13 | a0001c0001t0003a0001c0001t0018a0001c0001t0041others(10): Show | 22 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*10071T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 10071 | chr13 | 101712760 | |||||
| chr13:101712812
|
A | C | 15 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(12): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*10019T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 10019 | chr13 | 101712812 | |||||
| chr13:101712879
|
T | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*9952A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9952 | chr13 | 101712879 | |||||
| chr13:101713000
|
C | A | 1 | a0001c0001t0142 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9831G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9831 | chr13 | 101713000 | |||||
| chr13:101713098
|
C | G | 1 | a0001c0001t0119 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9733G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9733 | chr13 | 101713098 | |||||
| chr13:101713339
|
T | C | 16 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(13): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9492A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9492 | chr13 | 101713339 | |||||
| chr13:101713373
|
A | C | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9458T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9458 | chr13 | 101713373 | |||||
| chr13:101713449
|
G | A | 124 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(121): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*9382C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9382 | chr13 | 101713449 | |||||
| chr13:101713498
|
C | A | 1 | a0001c0001t0105 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9333G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9333 | chr13 | 101713498 | |||||
| chr13:101713646
|
T | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*9185A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 9185 | chr13 | 101713646 | |||||
| chr13:101713847
|
C | T | 1 | a0001c0001t0092 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8984G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8984 | chr13 | 101713847 | |||||
| chr13:101713856
|
G | A | 9 | a0001c0001t0010a0001c0001t0030a0001c0001t0071others(6): Show | 13 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8975C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8975 | chr13 | 101713856 | |||||
| chr13:101714024
|
T | C | 1 | a0001c0001t0150 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8807A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8807 | chr13 | 101714024 | |||||
| chr13:101714051
|
T | A | 1 | a0001c0001t0092 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8780A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8780 | chr13 | 101714051 | |||||
| chr13:101714116
|
C | G | 1 | a0001c0001t0092 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8715G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8715 | chr13 | 101714116 | |||||
| chr13:101714353
|
G | C | 1 | a0001c0001t0048 | 2 | HG02300.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8478C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8478 | chr13 | 101714353 | |||||
| chr13:101714381
|
C | T | 1 | a0001c0001t0068 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8450G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8450 | chr13 | 101714381 | |||||
| chr13:101714392
|
C | T | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0025others(10): Show | 28 | HG00323.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*8439G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8439 | chr13 | 101714392 | |||||
| chr13:101714475
|
A | G | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*8356T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8356 | chr13 | 101714475 | |||||
| chr13:101714665
|
A | G | 2 | a0001c0001t0133a0001c0001t0136 | 2 | HG01943.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8166T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8166 | chr13 | 101714665 | |||||
| chr13:101714766
|
T | C | 1 | a0001c0001t0151 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8065A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 8065 | chr13 | 101714766 | |||||
| chr13:101714900
|
AT | A | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0046others(2): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7930delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7930 | chr13 | 101714900 | |||||
| chr13:101714912
|
A | G | 6 | a0001c0001t0016a0001c0001t0023a0001c0001t0094others(3): Show | 10 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7919T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7919 | chr13 | 101714912 | |||||
| chr13:101715053
|
T | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7778A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7778 | chr13 | 101715053 | |||||
| chr13:101715092
|
A | G | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7739T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7739 | chr13 | 101715092 | |||||
| chr13:101715138
|
T | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(31): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7693A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7693 | chr13 | 101715138 | |||||
| chr13:101715195
|
C | T | 18 | a0001c0001t0031a0001c0001t0032a0001c0001t0033others(15): Show | 22 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7636G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7636 | chr13 | 101715195 | |||||
| chr13:101715343
|
T | G | 1 | a0001c0001t0119 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7488A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7488 | chr13 | 101715343 | |||||
| chr13:101715538
|
G | A | 16 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(13): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7293C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7293 | chr13 | 101715538 | |||||
| chr13:101715540
|
T | C | 1 | a0001c0001t0123 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7291A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7291 | chr13 | 101715540 | |||||
| chr13:101715706
|
G | T | 158 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(155): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*7125C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 7125 | chr13 | 101715706 | |||||
| chr13:101715844
|
A | G | 21 | a0001c0001t0013a0001c0001t0031a0001c0001t0032others(18): Show | 28 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*6987T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 6987 | chr13 | 101715844 | |||||
| chr13:101716094
|
A | G | 1 | a0001c0001t0122 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6737T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 6737 | chr13 | 101716094 | |||||
| chr13:101716791
|
C | CA | 119 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(116): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*6039dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 6039 | chr13 | 101716791 | |||||
| chr13:101716791
|
C | CAA | 32 | a0001c0001t0013a0001c0001t0019a0001c0001t0031others(29): Show | 43 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*6038_*6039dupTT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 6039 | chr13 | 101716791 | |||||
| chr13:101716913
|
T | C | 6 | a0001c0001t0062a0001c0001t0063a0001c0001t0064others(3): Show | 6 | HG00280.hp2 HG00408.hp2 HG01978.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5918A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5918 | chr13 | 101716913 | |||||
| chr13:101717019
|
C | A | 1 | a0001c0001t0151 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5812G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5812 | chr13 | 101717019 | |||||
| chr13:101717216
|
T | C | 1 | a0001c0001t0151 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5615A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5615 | chr13 | 101717216 | |||||
| chr13:101717256
|
C | G | 27 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(24): Show | 58 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*5575G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5575 | chr13 | 101717256 | |||||
| chr13:101717337
|
T | C | 1 | a0001c0002t0128 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5494A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5494 | chr13 | 101717337 | |||||
| chr13:101717357
|
A | C | 16 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(13): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5474T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5474 | chr13 | 101717357 | |||||
| chr13:101717611
|
T | G | 1 | a0001c0001t0088 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5220A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5220 | chr13 | 101717611 | |||||
| chr13:101717635
|
C | T | 1 | a0001c0001t0151 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5196G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5196 | chr13 | 101717635 | |||||
| chr13:101717664
|
TTC | T | 15 | a0001c0001t0002a0001c0001t0011a0001c0001t0022others(12): Show | 29 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5165_*5166delGA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5165 | chr13 | 101717664 | |||||
| chr13:101717708
|
T | A | 26 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(23): Show | 44 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5123A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 5123 | chr13 | 101717708 | |||||
| chr13:101717879
|
T | G | 2 | a0001c0001t0141a0001c0001t0142 | 2 | HG00438.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4952A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4952 | chr13 | 101717879 | |||||
| chr13:101717954
|
G | A | 4 | a0001c0001t0057a0001c0001t0106a0001c0001t0146others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4877C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4877 | chr13 | 101717954 | |||||
| chr13:101717971
|
G | A | 1 | a0001c0001t0071 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4860C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4860 | chr13 | 101717971 | |||||
| chr13:101718160
|
T | C | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(27): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*4671A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4671 | chr13 | 101718160 | |||||
| chr13:101718565
|
AATC | A | 53 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(50): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*4263_*4265delGAT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4263 | chr13 | 101718565 | |||||
| chr13:101718645
|
T | C | 27 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(24): Show | 57 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4186A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4186 | chr13 | 101718645 | |||||
| chr13:101718781
|
GA | G | 8 | a0001c0001t0024a0001c0001t0031a0001c0001t0032others(5): Show | 14 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4049delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4049 | chr13 | 101718781 | |||||
| chr13:101718782
|
A | G | 1 | a0001c0001t0158 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4049T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4049 | chr13 | 101718782 | |||||
| chr13:101718830
|
A | G | 1 | a0001c0001t0104 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4001T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 4001 | chr13 | 101718830 | |||||
| chr13:101718862
|
C | T | 1 | a0001c0001t0092 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3969G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3969 | chr13 | 101718862 | |||||
| chr13:101718896
|
G | A | 15 | a0001c0001t0013a0001c0001t0047a0001c0001t0081others(12): Show | 19 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3935C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3935 | chr13 | 101718896 | |||||
| chr13:101718933
|
AG | A | 1 | a0001c0001t0022 | 3 | NA18962.hp1 NA18992.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3897delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3897 | chr13 | 101718933 | |||||
| chr13:101718977
|
G | GA | 3 | a0001c0002t0014a0001c0002t0127a0001c0002t0128 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3853dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3853 | chr13 | 101718977 | |||||
| chr13:101719006
|
G | A | 3 | a0001c0002t0014a0001c0002t0127a0001c0002t0128 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3825C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3825 | chr13 | 101719006 | |||||
| chr13:101719008
|
T | C | 3 | a0001c0001t0034a0001c0001t0084a0001c0001t0135 | 4 | HG00099.hp2 HG01255.hp1 HG01257.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3823A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3823 | chr13 | 101719008 | |||||
| chr13:101719068
|
C | T | 1 | a0001c0001t0073 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3763G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3763 | chr13 | 101719068 | |||||
| chr13:101719140
|
T | C | 8 | a0001c0001t0031a0001c0001t0032a0001c0001t0033others(5): Show | 11 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3691A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3691 | chr13 | 101719140 | |||||
| chr13:101719169
|
C | T | 22 | a0001c0001t0006a0001c0001t0024a0001c0001t0034others(19): Show | 33 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3662G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3662 | chr13 | 101719169 | |||||
| chr13:101719170
|
G | A | 1 | a0001c0001t0121 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3661C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3661 | chr13 | 101719170 | |||||
| chr13:101719443
|
A | AAAT | 63 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(60): Show | 108 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3385_*3387dupATT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3387 | chr13 | 101719443 | |||||
| chr13:101719477
|
G | A | 2 | a0001c0001t0146a0001c0001t0148 | 2 | HG01884.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3354C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3354 | chr13 | 101719477 | |||||
| chr13:101719491
|
T | C | 1 | a0001c0001t0076 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3340A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3340 | chr13 | 101719491 | |||||
| chr13:101719548
|
C | A | 1 | a0001c0001t0036 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3283G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3283 | chr13 | 101719548 | |||||
| chr13:101719676
|
A | G | 1 | a0001c0001t0072 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3155T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3155 | chr13 | 101719676 | |||||
| chr13:101719686
|
C | T | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0046others(2): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3145G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 3145 | chr13 | 101719686 | |||||
| chr13:101719866
|
A | AG | 17 | a0001c0001t0006a0001c0001t0026a0001c0001t0034others(14): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2964dupC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2964 | chr13 | 101719866 | |||||
| chr13:101720129
|
GCAGA | G | 2 | a0001c0001t0035a0001c0001t0100 | 3 | HG02738.hp2 HG03942.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2698_*2701delTCTG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2698 | chr13 | 101720129 | |||||
| chr13:101720159
|
A | G | 1 | a0001c0001t0139 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2672T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2672 | chr13 | 101720159 | |||||
| chr13:101720530
|
C | CTG | 16 | a0001c0001t0016a0001c0001t0023a0001c0001t0033others(13): Show | 21 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2299_*2300dupCA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2300 | chr13 | 101720530 | |||||
| chr13:101720530
|
C | CTGTG | 7 | a0001c0001t0028a0001c0001t0032a0001c0001t0037others(4): Show | 10 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2297_*2300dupCACA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2300 | chr13 | 101720530 | |||||
| chr13:101720530
|
C | CTGTGTG | 15 | a0001c0001t0013a0001c0001t0019a0001c0001t0031others(12): Show | 21 | HG00099.hp1 HG01081.hp2 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2295_*2300dupCACA others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2300 | chr13 | 101720530 | |||||
| chr13:101720530
|
C | CTGTGTGT others(1): Show |
4 | a0001c0001t0068a0001c0001t0081a0001c0001t0096others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2293_*2300dupCACA others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2300 | chr13 | 101720530 | |||||
| chr13:101720530
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0080 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2291_*2300dupCACA others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2300 | chr13 | 101720530 | |||||
| chr13:101720530
|
C | G | 3 | a0001c0001t0057a0001c0001t0092a0001c0001t0106 | 3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2301G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2301 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTG | C | 44 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(41): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2299_*2300delCA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2299 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTGTG | C | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(28): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2297_*2300delCACA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2297 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTGTGTG | C | 7 | a0001c0001t0044a0001c0001t0047a0001c0001t0064others(4): Show | 9 | HG01109.hp1 HG01978.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2295_*2300delCACA others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2295 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTGTGTGT others(3): Show |
C | 3 | a0001c0002t0014a0001c0002t0127a0001c0002t0128 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2291_*2300delCACA others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2291 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0143 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289_*2300delCACA others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2289 | chr13 | 101720530 | |||||
| chr13:101720530
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0144 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287_*2300delCACA others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2287 | chr13 | 101720530 | |||||
| chr13:101720562
|
GTGTA | G | 3 | a0001c0001t0020a0001c0001t0067a0001c0001t0152 | 5 | HG00544.hp2 NA18941.hp2 NA19054.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2265_*2268delTACA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2265 | chr13 | 101720562 | |||||
| chr13:101720564
|
G | A | 1 | a0001c0001t0077 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2267C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2267 | chr13 | 101720564 | |||||
| chr13:101720566
|
A | G | 9 | a0001c0001t0028a0001c0001t0040a0001c0001t0061others(6): Show | 11 | HG01952.hp2 HG02615.hp2 HG03041.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2265T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2265 | chr13 | 101720566 | |||||
| chr13:101720611
|
T | C | 70 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(67): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2220A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2220 | chr13 | 101720611 | |||||
| chr13:101720621
|
C | A | 7 | a0001c0001t0016a0001c0001t0023a0001c0001t0061others(4): Show | 11 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2210G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2210 | chr13 | 101720621 | |||||
| chr13:101720684
|
A | G | 3 | a0001c0002t0014a0001c0002t0127a0001c0002t0128 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2147T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2147 | chr13 | 101720684 | |||||
| chr13:101720745
|
A | AAAAC | 21 | a0001c0001t0013a0001c0001t0019a0001c0001t0047others(18): Show | 27 | HG01081.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2082_*2085dupGTTT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2085 | chr13 | 101720745 | |||||
| chr13:101720786
|
T | C | 2 | a0001c0001t0090a0001c0001t0160 | 2 | HG02622.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2045A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 2045 | chr13 | 101720786 | |||||
| chr13:101721090
|
A | G | 1 | a0001c0001t0062 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1741 | chr13 | 101721090 | |||||
| chr13:101721164
|
TGAG | T | 5 | a0001c0001t0062a0001c0001t0063a0001c0001t0064others(2): Show | 5 | HG00280.hp2 HG01978.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1664_*1666delCTC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1664 | chr13 | 101721164 | |||||
| chr13:101721213
|
A | T | 140 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(137): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1618T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1618 | chr13 | 101721213 | |||||
| chr13:101721219
|
C | A | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(49): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1612G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1612 | chr13 | 101721219 | |||||
| chr13:101721384
|
T | TAA | 8 | a0001c0001t0016a0001c0001t0023a0001c0001t0094others(5): Show | 12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1445_*1446dupTT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1446 | chr13 | 101721384 | |||||
| chr13:101721440
|
C | CTTTA | 70 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(67): Show | 113 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1390dupTAAA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1390 | chr13 | 101721440 | |||||
| chr13:101721572
|
G | A | 2 | a0001c0001t0078a0001c0001t0126 | 2 | HG02109.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1259 | chr13 | 101721572 | |||||
| chr13:101721578
|
A | G | 1 | a0001c0001t0129 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1253T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1253 | chr13 | 101721578 | |||||
| chr13:101721658
|
CTAAT | C | 3 | a0001c0002t0014a0001c0002t0127a0001c0002t0128 | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1169_*1172delATTA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1169 | chr13 | 101721658 | |||||
| chr13:101721713
|
C | T | 1 | a0001c0001t0058 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1118G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1118 | chr13 | 101721713 | |||||
| chr13:101721768
|
C | T | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0046others(2): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 1063 | chr13 | 101721768 | |||||
| chr13:101721846
|
T | G | 1 | a0001c0001t0152 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 985 | chr13 | 101721846 | |||||
| chr13:101721858
|
C | CT | 63 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(60): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*972dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 972 | chr13 | 101721858 | |||||
| chr13:101722087
|
G | T | 2 | a0001c0001t0057a0001c0001t0106 | 2 | HG02572.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*744C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 744 | chr13 | 101722087 | |||||
| chr13:101722277
|
C | T | 3 | a0001c0001t0039a0001c0001t0053a0001c0001t0056 | 4 | HG01978.hp1 NA18977.hp2 NA19000.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*554G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 554 | chr13 | 101722277 | |||||
| chr13:101722320
|
T | C | 1 | a0001c0001t0093 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 511 | chr13 | 101722320 | |||||
| chr13:101722360
|
T | G | 7 | a0001c0001t0016a0001c0001t0023a0001c0001t0094others(4): Show | 11 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*471A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 471 | chr13 | 101722360 | |||||
| chr13:101722654
|
T | TG | 7 | a0001c0001t0096a0001c0001t0097a0001c0001t0098others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*176dupC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 176 | chr13 | 101722654 | |||||
| chr13:101722655
|
G | C | 2 | a0001c0001t0101a0001c0001t0155 | 2 | NA19066.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*176C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 5/5 | 176 | chr13 | 101722655 | |||||
| chr13:101916677
|
G | A | 1 | a0001c0001t0156 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 32 | chr13 | 101916677 | |||||
| chr13:101916738
|
C | T | 4 | a0001c0001t0025a0001c0001t0053a0001c0001t0054others(1): Show | 5 | NA18978.hp2 NA18986.hp2 NA18993.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 93 | chr13 | 101916738 | |||||
| chr13:101916757
|
G | A | 6 | a0001c0001t0024a0001c0001t0157a0001c0001t0158others(3): Show | 8 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-112C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 112 | chr13 | 101916757 | |||||
| chr13:101916782
|
G | T | 5 | a0001c0001t0017a0001c0001t0102a0001c0001t0103others(2): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-137C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 137 | chr13 | 101916782 | |||||
| chr13:101916792
|
G | C | 86 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(83): Show | 133 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 147 | chr13 | 101916792 | |||||
| chr13:101916792
|
G | T | 1 | a0001c0001t0052 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 147 | chr13 | 101916792 | |||||
| chr13:101916827
|
C | T | 2 | a0001c0001t0050a0001c0001t0051 | 2 | HG02886.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-182G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 182 | chr13 | 101916827 | |||||
| chr13:101916847
|
G | A | 1 | a0001c0001t0162 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-202C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 202 | chr13 | 101916847 | |||||
| chr13:101916891
|
C | G | 162 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(159): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
5_prime_UTR_variant | MODIFIER | c.-246G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/5 | 246 | chr13 | 101916891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:101722977
|
G | A | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.608-10C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101722977 | ||||||
| chr13:101723268
|
A | AAC | 163 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(160): Show | 163 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.608-303_608-302dup others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723268 | ||||||
| chr13:101723268
|
A | AACAC | 41 | a0001c0001t0001g0036a0001c0001t0013g0142a0001c0001t0013g0143others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.608-305_608-302dup others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723268 | ||||||
| chr13:101723507
|
T | C | 93 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.608-540A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723507 | ||||||
| chr13:101723758
|
G | A | 5 | a0001c0002t0014g0074a0001c0002t0014g0116a0001c0002t0014g0118others(2): Show | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-791C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723758 | ||||||
| chr13:101723816
|
ATGGT | A | 20 | a0001c0001t0006g0059a0001c0001t0006g0073a0001c0001t0006g0083others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.608-853_608-850del others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723816 | ||||||
| chr13:101723852
|
A | G | 85 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(82): Show | 85 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.608-885T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723852 | ||||||
| chr13:101723993
|
C | T | 2 | a0001c0001t0027g0026a0001c0001t0027g0046 | 2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.608-1026G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101723993 | ||||||
| chr13:101724091
|
A | G | 9 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-1124T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724091 | ||||||
| chr13:101724104
|
G | A | 2 | a0001c0001t0026g0027a0001c0001t0030g0032 | 2 | HG01256.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.608-1137C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724104 | ||||||
| chr13:101724208
|
G | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.608-1241C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724208 | ||||||
| chr13:101724286
|
A | C | 1 | a0001c0001t0072g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.608-1319T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724286 | ||||||
| chr13:101724431
|
C | G | 227 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.608-1464G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724431 | ||||||
| chr13:101724453
|
G | C | 1 | a0001c0001t0035g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.608-1486C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724453 | ||||||
| chr13:101724545
|
A | G | 9 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-1578T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724545 | ||||||
| chr13:101724597
|
A | AATATAT | 4 | a0001c0001t0103g0134a0001c0002t0014g0074a0001c0002t0127g0224others(1): Show | 4 | HG03041.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-1636_608-1631d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(3): Show |
8 | a0001c0001t0007g0037a0001c0001t0007g0052a0001c0001t0007g0081others(5): Show | 8 | HG01074.hp2 HG01928.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-1640_608-1631d others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(5): Show |
1 | a0001c0001t0088g0053 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.608-1642_608-1631d others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(7): Show |
1 | a0001c0001t0024g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.608-1644_608-1631d others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(9): Show |
6 | a0001c0001t0024g0261a0001c0001t0037g0066a0001c0001t0040g0189others(3): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-1646_608-1631d others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(11): Show |
1 | a0001c0001t0040g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.608-1648_608-1631d others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(13): Show |
3 | a0001c0001t0024g0259a0001c0001t0038g0064a0001c0001t0046g0148 | 3 | HG02486.hp2 HG02886.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.608-1650_608-1631d others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(15): Show |
1 | a0001c0001t0009g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.608-1652_608-1631d others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
A | AATATATA others(17): Show |
1 | a0001c0001t0087g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.608-1654_608-1631d others(26): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AAT | A | 9 | a0001c0001t0002g0096a0001c0001t0005g0067a0001c0001t0005g0103others(6): Show | 9 | HG00099.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-1632_608-1631d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATAT | A | 28 | a0001c0001t0002g0098a0001c0001t0005g0047a0001c0001t0005g0048others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.608-1634_608-1631d others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATATAT | A | 83 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0127others(80): Show | 83 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.608-1636_608-1631d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATATATA others(1): Show |
A | 65 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.608-1638_608-1631d others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATATATA others(3): Show |
A | 34 | a0001c0001t0006g0059a0001c0001t0006g0073a0001c0001t0006g0083others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.608-1640_608-1631d others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0061g0025a0001c0001t0092g0113 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.608-1642_608-1631d others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724597
|
AATATATA others(9): Show |
A | 2 | a0001c0001t0009g0241a0001c0001t0147g0220 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.608-1646_608-1631d others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724597 | ||||||
| chr13:101724623
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0134g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.608-1666_608-1657d others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724623 | ||||||
| chr13:101724631
|
T | A | 1 | a0001c0001t0123g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.608-1664A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724631 | ||||||
| chr13:101724687
|
T | TC | 261 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.608-1721dupG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724687 | ||||||
| chr13:101724689
|
A | T | 261 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.608-1722T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724689 | ||||||
| chr13:101724749
|
T | C | 90 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.608-1782A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724749 | ||||||
| chr13:101724868
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0108g0172 | 2 | NA18971.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.607+1744G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724868 | ||||||
| chr13:101724868
|
CAT | C | 9 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.607+1742_607+1743d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101724868 | ||||||
| chr13:101725469
|
A | C | 38 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.607+1143T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101725469 | ||||||
| chr13:101725543
|
T | A | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.607+1069A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101725543 | ||||||
| chr13:101726132
|
T | A | 233 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.607+480A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101726132 | ||||||
| chr13:101726204
|
T | G | 13 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+408A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101726204 | ||||||
| chr13:101726220
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.607+392T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101726220 | ||||||
| chr13:101726272
|
G | T | 4 | a0001c0001t0057g0086a0001c0001t0106g0163a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.607+340C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101726272 | ||||||
| chr13:101726552
|
A | G | 1 | a0001c0001t0145g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.607+60T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 4/4 | chr13 | 101726552 | ||||||
| chr13:101726931
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.409-121A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101726931 | ||||||
| chr13:101726945
|
C | T | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.409-135G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101726945 | ||||||
| chr13:101727217
|
T | C | 2 | a0001c0001t0002g0109a0001c0001t0108g0172 | 2 | NA18971.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.409-407A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727217 | ||||||
| chr13:101727266
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.409-456A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727266 | ||||||
| chr13:101727271
|
C | T | 4 | a0001c0001t0057g0086a0001c0001t0106g0163a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-461G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727271 | ||||||
| chr13:101727344
|
A | G | 1 | a0001c0001t0035g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.409-534T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727344 | ||||||
| chr13:101727398
|
T | A | 2 | a0001c0001t0030g0023a0001c0001t0074g0122 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.409-588A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727398 | ||||||
| chr13:101727817
|
C | G | 98 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.409-1007G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727817 | ||||||
| chr13:101727935
|
A | T | 37 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.409-1125T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101727935 | ||||||
| chr13:101728078
|
A | C | 4 | a0001c0001t0020g0187a0001c0001t0020g0217a0001c0001t0020g0250others(1): Show | 4 | HG00544.hp2 NA18941.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-1268T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101728078 | ||||||
| chr13:101728656
|
T | TA | 107 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.409-1847_409-1846i others(3): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101728656 | ||||||
| chr13:101728658
|
T | C | 107 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.409-1848A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101728658 | ||||||
| chr13:101728919
|
T | A | 1 | a0001c0001t0148g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.409-2109A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101728919 | ||||||
| chr13:101728951
|
T | G | 108 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.409-2141A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101728951 | ||||||
| chr13:101729031
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-2221G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101729031 | ||||||
| chr13:101729349
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.409-2539T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101729349 | ||||||
| chr13:101729756
|
C | CCAAAT | 229 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.409-2947_409-2946i others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101729756 | ||||||
| chr13:101729805
|
A | G | 8 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.409-2995T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101729805 | ||||||
| chr13:101730012
|
C | A | 95 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.409-3202G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730012 | ||||||
| chr13:101730181
|
G | A | 5 | a0001c0002t0014g0074a0001c0002t0014g0116a0001c0002t0014g0118others(2): Show | 5 | HG01192.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-3371C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730181 | ||||||
| chr13:101730222
|
G | A | 20 | a0001c0001t0006g0059a0001c0001t0006g0073a0001c0001t0006g0083others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.409-3412C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730222 | ||||||
| chr13:101730261
|
A | C | 1 | a0001c0001t0031g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.409-3451T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730261 | ||||||
| chr13:101730654
|
T | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-3844A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730654 | ||||||
| chr13:101730907
|
G | A | 1 | a0001c0001t0092g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.409-4097C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101730907 | ||||||
| chr13:101731184
|
A | C | 38 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.409-4374T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101731184 | ||||||
| chr13:101731330
|
T | G | 23 | a0001c0001t0006g0059a0001c0001t0006g0073a0001c0001t0006g0083others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.409-4520A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101731330 | ||||||
| chr13:101731549
|
C | T | 9 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-4739G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101731549 | ||||||
| chr13:101731833
|
G | C | 2 | a0001c0001t0061g0025a0001c0001t0092g0113 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.409-5023C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101731833 | ||||||
| chr13:101732302
|
A | C | 9 | a0001c0001t0019g0227a0001c0001t0019g0244a0001c0001t0019g0247others(6): Show | 9 | HG01081.hp2 HG01975.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.409-5492T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101732302 | ||||||
| chr13:101732439
|
T | G | 1 | a0001c0001t0143g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.409-5629A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101732439 | ||||||
| chr13:101732660
|
AATAAG | A | 56 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(53): Show | 56 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.409-5855_409-5851d others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101732660 | ||||||
| chr13:101732716
|
T | C | 1 | a0001c0001t0092g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.409-5906A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101732716 | ||||||
| chr13:101732949
|
T | C | 6 | a0001c0001t0004g0057a0001c0001t0004g0070a0001c0001t0004g0071others(3): Show | 6 | HG01496.hp1 HG01928.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-6139A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101732949 | ||||||
| chr13:101733007
|
T | C | 10 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-6197A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733007 | ||||||
| chr13:101733057
|
T | C | 11 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(8): Show | 11 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-6247A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733057 | ||||||
| chr13:101733221
|
T | C | 2 | a0001c0001t0047g0165a0001c0001t0047g0213 | 2 | HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.409-6411A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733221 | ||||||
| chr13:101733287
|
A | G | 88 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.409-6477T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733287 | ||||||
| chr13:101733456
|
G | C | 5 | a0001c0001t0004g0088a0001c0001t0012g0216a0001c0001t0021g0210others(2): Show | 5 | HG02015.hp2 HG02523.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-6646C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733456 | ||||||
| chr13:101733591
|
C | CA | 11 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(8): Show | 11 | HG01978.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-6782dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733591 | ||||||
| chr13:101733591
|
CA | C | 74 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(71): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.409-6782delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733591 | ||||||
| chr13:101733591
|
CAA | C | 20 | a0001c0001t0003g0058a0001c0001t0012g0237a0001c0001t0013g0142others(17): Show | 20 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.409-6783_409-6782d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733591 | ||||||
| chr13:101733611
|
A | G | 96 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.409-6801T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733611 | ||||||
| chr13:101733612
|
AGAGAGAG others(2): Show |
A | 96 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.409-6811_409-6803d others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733612 | ||||||
| chr13:101733614
|
AGAGAGAG | A | 3 | a0001c0001t0008g0208a0001c0001t0025g0007a0001c0001t0029g0099 | 3 | NA18978.hp1 NA18993.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.409-6811_409-6805d others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733614 | ||||||
| chr13:101733720
|
C | A | 2 | a0001c0001t0062g0056a0001c0001t0109g0199 | 2 | HG04184.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.409-6910G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733720 | ||||||
| chr13:101733747
|
G | A | 3 | a0001c0001t0032g0039a0001c0001t0032g0060a0001c0001t0132g0184 | 3 | HG01256.hp2 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.409-6937C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733747 | ||||||
| chr13:101733849
|
TTA | T | 4 | a0001c0001t0007g0042a0001c0001t0007g0043a0001c0001t0037g0066others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-7041_409-7040d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733849 | ||||||
| chr13:101733901
|
A | G | 11 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(8): Show | 11 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-7091T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101733901 | ||||||
| chr13:101734024
|
G | A | 2 | a0001c0001t0048g0168a0001c0001t0048g0206 | 2 | HG02300.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.409-7214C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734024 | ||||||
| chr13:101734269
|
G | A | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.409-7459C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734269 | ||||||
| chr13:101734347
|
A | T | 10 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-7537T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734347 | ||||||
| chr13:101734491
|
T | A | 1 | a0001c0001t0030g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.409-7681A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734491 | ||||||
| chr13:101734789
|
G | A | 4 | a0001c0001t0057g0086a0001c0001t0106g0163a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-7979C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734789 | ||||||
| chr13:101734920
|
T | C | 2 | a0001c0001t0057g0086a0001c0001t0106g0163 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-8110A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734920 | ||||||
| chr13:101734963
|
C | T | 100 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(97): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.409-8153G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101734963 | ||||||
| chr13:101735015
|
A | C | 3 | a0001c0001t0026g0027a0001c0001t0026g0123a0001c0001t0059g0034 | 3 | HG01169.hp2 HG01256.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.409-8205T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735015 | ||||||
| chr13:101735080
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.409-8270C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735080 | ||||||
| chr13:101735569
|
G | A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-8759C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735569 | ||||||
| chr13:101735670
|
G | GA | 46 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(43): Show | 46 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.409-8861dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735670 | ||||||
| chr13:101735709
|
C | T | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-8899G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735709 | ||||||
| chr13:101735816
|
C | G | 3 | a0001c0001t0058g0068a0001c0001t0078g0094a0001c0001t0126g0161 | 3 | HG01106.hp1 HG02109.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.409-9006G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735816 | ||||||
| chr13:101735830
|
G | A | 1 | a0001c0001t0152g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.409-9020C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101735830 | ||||||
| chr13:101736233
|
CATAACT | C | 3 | a0001c0001t0033g0049a0001c0001t0033g0095a0001c0001t0069g0024 | 3 | HG02074.hp2 NA18992.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.409-9429_409-9424d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101736233 | ||||||
| chr13:101736765
|
G | A | 261 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.409-9955C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101736765 | ||||||
| chr13:101736833
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.409-10023T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101736833 | ||||||
| chr13:101736851
|
C | A | 261 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.409-10041G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101736851 | ||||||
| chr13:101737016
|
T | TTCTATTT others(317): Show |
1 | a0001c0001t0056g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(328): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(320): Show |
1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(331): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(331): Show |
1 | a0001c0001t0122g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.409-10207_409-1020 others(342): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(330): Show |
1 | a0001c0001t0008g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(341): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(331): Show |
23 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0003g0076others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.409-10207_409-1020 others(342): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(332): Show |
2 | a0001c0001t0034g0038a0001c0001t0034g0054 | 2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.409-10207_409-1020 others(343): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(332): Show |
5 | a0001c0001t0006g0059a0001c0001t0006g0073a0001c0001t0134g0180others(2): Show | 5 | HG00597.hp1 HG01496.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-10207_409-1020 others(343): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(332): Show |
1 | a0001c0001t0008g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.409-10207_409-1020 others(343): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(331): Show |
1 | a0001c0001t0106g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(342): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(332): Show |
31 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0075others(28): Show | 31 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.409-10207_409-1020 others(343): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(333): Show |
1 | a0001c0001t0133g0211 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(344): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(333): Show |
3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0011g0150 | 3 | HG01099.hp2 HG01516.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.409-10207_409-1020 others(344): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(333): Show |
17 | a0001c0001t0003g0030a0001c0001t0007g0081a0001c0001t0018g0236others(14): Show | 17 | HG00642.hp1 HG01169.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.409-10207_409-1020 others(344): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(334): Show |
1 | a0001c0001t0086g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(345): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(334): Show |
1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(345): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(335): Show |
1 | a0001c0001t0060g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.409-10207_409-1020 others(346): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737016
|
T | TTCTATTT others(335): Show |
2 | a0001c0001t0001g0093a0001c0001t0118g0242 | 2 | HG03195.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.409-10207_409-1020 others(346): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737016 | ||||||
| chr13:101737099
|
C | T | 113 | a0001c0001t0001g0132a0001c0001t0002g0055a0001c0001t0002g0065others(110): Show | 113 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.409-10289G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737099 | ||||||
| chr13:101737197
|
A | T | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-10387T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737197 | ||||||
| chr13:101737203
|
A | G | 8 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(5): Show | 8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.409-10393T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737203 | ||||||
| chr13:101737225
|
A | G | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0022g0196 | 3 | NA18962.hp1 NA18992.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.409-10415T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737225 | ||||||
| chr13:101737357
|
C | A | 1 | a0001c0001t0024g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.409-10547G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737357 | ||||||
| chr13:101737436
|
CA | C | 259 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.409-10627delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737436 | ||||||
| chr13:101737443
|
A | T | 110 | a0001c0001t0001g0132a0001c0001t0002g0055a0001c0001t0002g0065others(107): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.409-10633T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737443 | ||||||
| chr13:101737993
|
A | G | 1 | a0001c0001t0108g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.409-11183T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101737993 | ||||||
| chr13:101738501
|
G | A | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-11691C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738501 | ||||||
| chr13:101738676
|
T | C | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-11866A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738676 | ||||||
| chr13:101738734
|
A | T | 93 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.409-11924T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738734 | ||||||
| chr13:101738736
|
T | C | 1 | a0001c0001t0035g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.409-11926A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738736 | ||||||
| chr13:101738956
|
G | GTA | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-12148_409-1214 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738956 | ||||||
| chr13:101738956
|
GTA | G | 35 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0009g0241others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.409-12148_409-1214 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738956 | ||||||
| chr13:101738956
|
GTATA | G | 93 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.409-12150_409-1214 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738956 | ||||||
| chr13:101738958
|
A | G | 110 | a0001c0001t0001g0132a0001c0001t0002g0055a0001c0001t0002g0065others(107): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.409-12148T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738958 | ||||||
| chr13:101738974
|
G | A | 2 | a0001c0001t0061g0025a0001c0001t0151g0147 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-12164C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738974 | ||||||
| chr13:101738992
|
A | G | 5 | a0001c0001t0004g0057a0001c0001t0004g0070a0001c0001t0004g0071others(2): Show | 5 | HG01496.hp1 HG01928.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-12182T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101738992 | ||||||
| chr13:101739014
|
C | CTA | 13 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-12206_409-1220 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739014 | ||||||
| chr13:101739043
|
A | C | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.409-12233T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739043 | ||||||
| chr13:101739089
|
G | GTA | 5 | a0001c0001t0018g0236a0001c0001t0024g0259a0001c0001t0057g0086others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-12281_409-1228 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739089 | ||||||
| chr13:101739108
|
C | T | 30 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0009g0159others(27): Show | 30 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.409-12298G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739108 | ||||||
| chr13:101739110
|
T | C | 23 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0009g0159others(20): Show | 23 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.409-12300A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739110 | ||||||
| chr13:101739110
|
T | TAC | 7 | a0001c0001t0017g0135a0001c0001t0024g0261a0001c0001t0026g0027others(4): Show | 7 | HG00099.hp1 HG01256.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-12301_409-1230 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739110 | ||||||
| chr13:101739111
|
G | A | 31 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0009g0159others(28): Show | 31 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.409-12301C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739111 | ||||||
| chr13:101739111
|
G | GTA | 4 | a0001c0001t0017g0136a0001c0001t0057g0086a0001c0001t0105g0133others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-12303_409-1230 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739111 | ||||||
| chr13:101739111
|
GTA | G | 189 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(186): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.409-12303_409-1230 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739111 | ||||||
| chr13:101739113
|
A | G | 30 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0009g0159others(27): Show | 30 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.409-12303T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739113 | ||||||
| chr13:101739401
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0151g0147 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-12591A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739401 | ||||||
| chr13:101739567
|
G | A | 108 | a0001c0001t0001g0132a0001c0001t0002g0055a0001c0001t0002g0065others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.409-12757C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739567 | ||||||
| chr13:101739584
|
G | A | 2 | a0001c0001t0035g0089a0001c0001t0100g0084 | 2 | HG03942.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.409-12774C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739584 | ||||||
| chr13:101739629
|
A | G | 1 | a0001c0001t0008g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.409-12819T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739629 | ||||||
| chr13:101739886
|
CCAGTAGT others(37): Show |
C | 1 | a0001c0001t0067g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.409-13120_409-1307 others(48): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101739886 | ||||||
| chr13:101740292
|
G | A | 2 | a0001c0001t0061g0025a0001c0001t0151g0147 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-13482C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101740292 | ||||||
| chr13:101740321
|
C | T | 8 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(5): Show | 8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.409-13511G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101740321 | ||||||
| chr13:101740665
|
C | CA | 13 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-13856dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101740665 | ||||||
| chr13:101741047
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-14237G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741047 | ||||||
| chr13:101741299
|
G | T | 1 | a0001c0001t0027g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.409-14489C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741299 | ||||||
| chr13:101741474
|
A | G | 2 | a0001c0001t0057g0086a0001c0001t0105g0133 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-14664T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741474 | ||||||
| chr13:101741504
|
G | C | 13 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-14694C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741504 | ||||||
| chr13:101741634
|
T | TA | 16 | a0001c0001t0009g0159a0001c0001t0015g0121a0001c0001t0031g0035others(13): Show | 16 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-14825dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741634 | ||||||
| chr13:101741634
|
TA | T | 126 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.409-14825delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741634 | ||||||
| chr13:101741775
|
C | T | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-14965G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101741775 | ||||||
| chr13:101742066
|
T | C | 1 | a0001c0001t0033g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.409-15256A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101742066 | ||||||
| chr13:101742660
|
A | T | 1 | a0001c0001t0121g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.409-15850T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101742660 | ||||||
| chr13:101743430
|
A | T | 11 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(8): Show | 11 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.409-16620T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101743430 | ||||||
| chr13:101743434
|
T | A | 6 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(3): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-16624A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101743434 | ||||||
| chr13:101743531
|
C | A | 20 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0009g0241others(17): Show | 20 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.409-16721G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101743531 | ||||||
| chr13:101743639
|
G | C | 2 | a0001c0001t0047g0165a0001c0001t0047g0213 | 2 | HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.409-16829C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101743639 | ||||||
| chr13:101743823
|
TA | T | 22 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0009g0241others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.409-17014delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101743823 | ||||||
| chr13:101744208
|
G | A | 2 | a0001c0001t0017g0135a0001c0001t0050g0001 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.409-17398C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101744208 | ||||||
| chr13:101744343
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409-17533C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101744343 | ||||||
| chr13:101744725
|
C | A | 149 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.409-17915G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101744725 | ||||||
| chr13:101745051
|
G | C | 26 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0009g0241others(23): Show | 26 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.409-18241C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745051 | ||||||
| chr13:101745061
|
T | A | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-18251A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745061 | ||||||
| chr13:101745084
|
G | C | 1 | a0001c0001t0123g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.409-18274C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745084 | ||||||
| chr13:101745275
|
A | T | 2 | a0001c0001t0061g0025a0001c0001t0151g0147 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-18465T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745275 | ||||||
| chr13:101745340
|
C | A | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-18530G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745340 | ||||||
| chr13:101745553
|
T | C | 13 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-18743A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745553 | ||||||
| chr13:101745609
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.409-18799C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745609 | ||||||
| chr13:101745641
|
T | G | 10 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-18831A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745641 | ||||||
| chr13:101745787
|
A | G | 2 | a0001c0001t0061g0025a0001c0001t0151g0147 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-18977T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745787 | ||||||
| chr13:101745797
|
A | C | 13 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-18987T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101745797 | ||||||
| chr13:101746312
|
T | C | 1 | a0001c0001t0159g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.409-19502A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101746312 | ||||||
| chr13:101746411
|
A | T | 1 | a0001c0002t0128g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.409-19601T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101746411 | ||||||
| chr13:101747075
|
A | G | 1 | a0001c0001t0105g0133 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.409-20265T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101747075 | ||||||
| chr13:101747085
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-20275A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101747085 | ||||||
| chr13:101747614
|
T | C | 13 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-20804A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101747614 | ||||||
| chr13:101747939
|
T | G | 3 | a0001c0001t0016g0010a0001c0001t0023g0157a0001c0001t0023g0158 | 3 | HG02572.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-21129A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101747939 | ||||||
| chr13:101747963
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-21153T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101747963 | ||||||
| chr13:101748081
|
A | G | 101 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(98): Show | 101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.409-21271T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748081 | ||||||
| chr13:101748447
|
A | G | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.409-21637T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748447 | ||||||
| chr13:101748530
|
C | T | 1 | a0001c0001t0086g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.409-21720G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748530 | ||||||
| chr13:101748534
|
G | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.409-21724C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748534 | ||||||
| chr13:101748549
|
A | G | 25 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0009g0241others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.409-21739T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748549 | ||||||
| chr13:101748747
|
TA | T | 86 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0002g0098others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-21938delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748747 | ||||||
| chr13:101748747
|
TAA | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.409-21939_409-2193 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748747 | ||||||
| chr13:101748747
|
TAAA | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0003g0031others(16): Show | 19 | HG00438.hp2 HG01099.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.409-21940_409-2193 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748747 | ||||||
| chr13:101748922
|
G | T | 151 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.409-22112C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101748922 | ||||||
| chr13:101749136
|
C | T | 1 | a0001c0001t0148g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.409-22326G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101749136 | ||||||
| chr13:101749218
|
G | A | 11 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-22408C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101749218 | ||||||
| chr13:101749500
|
A | C | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-22690T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101749500 | ||||||
| chr13:101749744
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.409-22934C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101749744 | ||||||
| chr13:101749937
|
G | C | 2 | a0001c0001t0043g0253a0001c0001t0043g0254 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.409-23127C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101749937 | ||||||
| chr13:101750335
|
T | C | 179 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.409-23525A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750335 | ||||||
| chr13:101750429
|
A | C | 4 | a0001c0001t0017g0139a0001c0001t0093g0111a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-23619T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750429 | ||||||
| chr13:101750625
|
G | T | 12 | a0001c0001t0031g0035a0001c0001t0031g0108a0001c0001t0032g0039others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-23815C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750625 | ||||||
| chr13:101750705
|
A | G | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-23895T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750705 | ||||||
| chr13:101750765
|
C | T | 2 | a0001c0001t0021g0210a0001c0001t0041g0226 | 2 | HG00597.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.409-23955G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750765 | ||||||
| chr13:101750766
|
C | A | 24 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(21): Show | 24 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.409-23956G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750766 | ||||||
| chr13:101750893
|
A | C | 25 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(22): Show | 25 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.409-24083T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750893 | ||||||
| chr13:101750900
|
A | G | 1 | a0001c0001t0037g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.409-24090T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750900 | ||||||
| chr13:101750904
|
A | G | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-24094T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101750904 | ||||||
| chr13:101751014
|
CA | C | 3 | a0001c0001t0001g0033a0001c0001t0006g0097a0001c0001t0067g0091 | 3 | HG00323.hp1 NA19065.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.409-24205delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751014 | ||||||
| chr13:101751322
|
G | C | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-24512C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751322 | ||||||
| chr13:101751493
|
A | C | 1 | a0001c0001t0082g0072 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.409-24683T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751493 | ||||||
| chr13:101751556
|
T | C | 13 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-24746A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751556 | ||||||
| chr13:101751660
|
T | G | 7 | a0001c0001t0009g0241a0001c0001t0097g0020a0001c0001t0098g0014others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-24850A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751660 | ||||||
| chr13:101751834
|
A | G | 25 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(22): Show | 25 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.409-25024T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751834 | ||||||
| chr13:101751876
|
AT | A | 24 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(21): Show | 24 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.409-25067delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751876 | ||||||
| chr13:101751877
|
T | A | 1 | a0001c0001t0114g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.409-25067A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751877 | ||||||
| chr13:101751888
|
T | A | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-25078A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751888 | ||||||
| chr13:101751952
|
A | C | 173 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(170): Show | 173 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.409-25142T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101751952 | ||||||
| chr13:101752076
|
T | C | 25 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(22): Show | 25 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.409-25266A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752076 | ||||||
| chr13:101752140
|
C | T | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-25330G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752140 | ||||||
| chr13:101752229
|
A | C | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-25419T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752229 | ||||||
| chr13:101752295
|
A | G | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-25485T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752295 | ||||||
| chr13:101752606
|
T | G | 256 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.409-25796A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752606 | ||||||
| chr13:101752615
|
G | A | 26 | a0001c0001t0001g0093a0001c0001t0010g0153a0001c0001t0010g0201others(23): Show | 26 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.409-25805C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752615 | ||||||
| chr13:101752740
|
A | C | 25 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(22): Show | 25 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.409-25930T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101752740 | ||||||
| chr13:101753270
|
TACACACA others(23): Show |
T | 11 | a0001c0001t0010g0153a0001c0001t0010g0201a0001c0001t0010g0248others(8): Show | 11 | HG00423.hp1 HG01081.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.409-26490_409-2646 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753270 | ||||||
| chr13:101753298
|
G | GAC | 6 | a0001c0001t0016g0012a0001c0001t0029g0115a0001c0001t0103g0134others(3): Show | 6 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-26490_409-2648 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753298 | ||||||
| chr13:101753298
|
GAC | G | 174 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.409-26490_409-2648 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753298 | ||||||
| chr13:101753298
|
GACAC | G | 26 | a0001c0001t0002g0101a0001c0001t0009g0241a0001c0001t0028g0018others(23): Show | 26 | HG00408.hp1 HG01175.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.409-26492_409-2648 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753298 | ||||||
| chr13:101753298
|
GACACAC | G | 3 | a0001c0001t0009g0159a0001c0001t0012g0237a0001c0001t0113g0234 | 3 | HG01255.hp2 HG03139.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.409-26494_409-2648 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753298 | ||||||
| chr13:101753340
|
T | C | 4 | a0001c0001t0010g0201a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG00423.hp1 HG02015.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-26530A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753340 | ||||||
| chr13:101753396
|
A | G | 11 | a0001c0001t0016g0010a0001c0001t0016g0012a0001c0001t0016g0130others(8): Show | 11 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.409-26586T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753396 | ||||||
| chr13:101753635
|
T | C | 21 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0013g0142others(18): Show | 21 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.409-26825A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753635 | ||||||
| chr13:101753803
|
C | CA | 20 | a0001c0001t0003g0058a0001c0001t0006g0083a0001c0001t0007g0037others(17): Show | 20 | HG00642.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.409-26994dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753803 | ||||||
| chr13:101753803
|
CA | C | 14 | a0001c0001t0003g0076a0001c0001t0004g0071a0001c0001t0017g0139others(11): Show | 14 | HG00438.hp2 HG01884.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.409-26994delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753803 | ||||||
| chr13:101753835
|
C | G | 11 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-27025G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101753835 | ||||||
| chr13:101754010
|
A | G | 13 | a0001c0001t0001g0132a0001c0001t0031g0035a0001c0001t0031g0108others(10): Show | 13 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-27200T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754010 | ||||||
| chr13:101754064
|
T | G | 2 | a0001c0001t0011g0150a0001c0001t0138g0222 | 2 | HG00597.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.409-27254A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754064 | ||||||
| chr13:101754068
|
G | A | 2 | a0001c0001t0107g0175a0001c0001t0145g0174 | 2 | HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.409-27258C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754068 | ||||||
| chr13:101754296
|
G | C | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.409-27486C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754296 | ||||||
| chr13:101754869
|
GA | G | 229 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.409-28060delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754869 | ||||||
| chr13:101754961
|
A | T | 220 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.409-28151T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754961 | ||||||
| chr13:101754964
|
T | C | 2 | a0001c0001t0009g0159a0001c0001t0092g0113 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.409-28154A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101754964 | ||||||
| chr13:101755007
|
C | G | 228 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.409-28197G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755007 | ||||||
| chr13:101755297
|
C | G | 1 | a0001c0001t0004g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.409-28487G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755297 | ||||||
| chr13:101755359
|
C | A | 1 | a0001c0001t0113g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.409-28549G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755359 | ||||||
| chr13:101755376
|
T | C | 81 | a0001c0001t0001g0033a0001c0001t0001g0093a0001c0001t0002g0055others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.409-28566A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755376 | ||||||
| chr13:101755409
|
C | CAGG | 235 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(232): Show | 235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.409-28602_409-2860 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755409 | ||||||
| chr13:101755490
|
C | T | 3 | a0001c0001t0133g0211a0001c0001t0134g0180a0001c0001t0136g0204 | 3 | HG01496.hp2 HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.409-28680G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755490 | ||||||
| chr13:101755517
|
A | G | 1 | a0001c0001t0041g0209 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.409-28707T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755517 | ||||||
| chr13:101755549
|
TAAATC | T | 4 | a0001c0001t0017g0139a0001c0001t0093g0111a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-28744_409-2874 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755549 | ||||||
| chr13:101755711
|
G | A | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.409-28901C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755711 | ||||||
| chr13:101755714
|
T | G | 1 | a0001c0001t0026g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.409-28904A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755714 | ||||||
| chr13:101755889
|
T | C | 1 | a0001c0001t0005g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.409-29079A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101755889 | ||||||
| chr13:101756072
|
C | T | 4 | a0001c0001t0020g0217a0001c0001t0020g0250a0001c0001t0140g0192others(1): Show | 4 | HG00438.hp1 HG00544.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-29262G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756072 | ||||||
| chr13:101756088
|
C | A | 1 | a0001c0001t0064g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.409-29278G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756088 | ||||||
| chr13:101756240
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-29430A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756240 | ||||||
| chr13:101756510
|
G | A | 5 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(2): Show | 5 | HG02109.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-29700C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756510 | ||||||
| chr13:101756596
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0007g0081a0001c0001t0063g0090 | 3 | HG00280.hp2 HG01928.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.409-29786C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756596 | ||||||
| chr13:101756638
|
C | G | 6 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(3): Show | 6 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-29828G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756638 | ||||||
| chr13:101756688
|
G | A | 1 | a0001c0001t0104g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.409-29878C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756688 | ||||||
| chr13:101756739
|
C | A | 103 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.409-29929G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756739 | ||||||
| chr13:101756751
|
AAAAC | A | 5 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(2): Show | 5 | HG02109.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-29945_409-2994 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756751 | ||||||
| chr13:101756870
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-30060A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756870 | ||||||
| chr13:101756887
|
A | G | 4 | a0001c0001t0017g0139a0001c0001t0093g0111a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-30077T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101756887 | ||||||
| chr13:101757197
|
G | C | 2 | a0001c0001t0003g0110a0001c0001t0110g0182 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.409-30387C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101757197 | ||||||
| chr13:101757288
|
C | T | 3 | a0001c0001t0081g0120a0001c0001t0102g0138a0001c0001t0130g0219 | 3 | HG01884.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.409-30478G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101757288 | ||||||
| chr13:101757484
|
T | C | 1 | a0001c0001t0100g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409-30674A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101757484 | ||||||
| chr13:101757686
|
T | C | 2 | a0001c0001t0057g0086a0001c0001t0105g0133 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-30876A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101757686 | ||||||
| chr13:101758020
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-31210A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758020 | ||||||
| chr13:101758646
|
C | T | 90 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.409-31836G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758646 | ||||||
| chr13:101758649
|
T | C | 2 | a0001c0001t0003g0110a0001c0001t0110g0182 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.409-31839A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758649 | ||||||
| chr13:101758683
|
A | G | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.409-31873T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758683 | ||||||
| chr13:101758696
|
C | G | 75 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(72): Show | 75 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.409-31886G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758696 | ||||||
| chr13:101758816
|
A | T | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-32006T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758816 | ||||||
| chr13:101758856
|
T | A | 11 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-32046A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101758856 | ||||||
| chr13:101759226
|
C | T | 11 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-32416G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759226 | ||||||
| chr13:101759385
|
C | T | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-32575G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759385 | ||||||
| chr13:101759412
|
G | A | 9 | a0001c0001t0017g0139a0001c0001t0081g0120a0001c0001t0093g0111others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-32602C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759412 | ||||||
| chr13:101759569
|
G | T | 11 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-32759C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759569 | ||||||
| chr13:101759630
|
T | C | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-32820A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759630 | ||||||
| chr13:101759715
|
G | T | 1 | a0001c0001t0042g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.409-32905C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759715 | ||||||
| chr13:101759724
|
T | C | 159 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(156): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.409-32914A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759724 | ||||||
| chr13:101759847
|
G | A | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-33037C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759847 | ||||||
| chr13:101759884
|
T | A | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-33074A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759884 | ||||||
| chr13:101759964
|
G | A | 63 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.409-33154C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101759964 | ||||||
| chr13:101760110
|
A | T | 1 | a0001c0001t0020g0217 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.409-33300T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101760110 | ||||||
| chr13:101760474
|
A | T | 92 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.409-33664T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101760474 | ||||||
| chr13:101760706
|
T | C | 1 | a0001c0001t0017g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.409-33896A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101760706 | ||||||
| chr13:101760748
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-33938C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101760748 | ||||||
| chr13:101760991
|
A | C | 96 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.409-34181T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101760991 | ||||||
| chr13:101761078
|
T | C | 1 | a0001c0001t0074g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.409-34268A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761078 | ||||||
| chr13:101761166
|
T | A | 5 | a0001c0001t0002g0055a0001c0001t0002g0098a0001c0001t0036g0061others(2): Show | 5 | HG03490.hp1 HG03492.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-34356A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761166 | ||||||
| chr13:101761230
|
A | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-34420T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761230 | ||||||
| chr13:101761324
|
G | C | 105 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.409-34514C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761324 | ||||||
| chr13:101761325
|
A | T | 105 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.409-34515T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761325 | ||||||
| chr13:101761675
|
G | A | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-34865C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761675 | ||||||
| chr13:101761734
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-34924A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761734 | ||||||
| chr13:101761892
|
C | T | 1 | a0001c0001t0146g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.409-35082G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761892 | ||||||
| chr13:101761932
|
G | A | 16 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(13): Show | 16 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-35122C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761932 | ||||||
| chr13:101761955
|
A | T | 1 | a0001c0001t0009g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.409-35145T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761955 | ||||||
| chr13:101761970
|
T | C | 235 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.409-35160A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101761970 | ||||||
| chr13:101762015
|
G | A | 231 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.409-35205C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762015 | ||||||
| chr13:101762028
|
A | T | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-35218T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762028 | ||||||
| chr13:101762067
|
T | C | 230 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.409-35257A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762067 | ||||||
| chr13:101762521
|
T | C | 1 | a0001c0001t0161g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.409-35711A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762521 | ||||||
| chr13:101762715
|
T | C | 236 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.409-35905A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762715 | ||||||
| chr13:101762861
|
T | G | 1 | a0001c0001t0042g0231 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.409-36051A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762861 | ||||||
| chr13:101762925
|
C | G | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-36115G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762925 | ||||||
| chr13:101762988
|
C | A | 16 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(13): Show | 16 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-36178G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101762988 | ||||||
| chr13:101763012
|
C | T | 4 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-36202G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763012 | ||||||
| chr13:101763057
|
A | G | 12 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.409-36247T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763057 | ||||||
| chr13:101763194
|
TAC | T | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-36386_409-3638 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763194 | ||||||
| chr13:101763292
|
G | C | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.409-36482C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763292 | ||||||
| chr13:101763415
|
T | C | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-36605A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763415 | ||||||
| chr13:101763469
|
A | G | 86 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-36659T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763469 | ||||||
| chr13:101763594
|
C | T | 15 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-36784G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763594 | ||||||
| chr13:101763615
|
T | C | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-36805A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763615 | ||||||
| chr13:101763677
|
T | C | 1 | a0001c0001t0004g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.409-36867A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763677 | ||||||
| chr13:101763688
|
C | T | 2 | a0001c0001t0091g0117a0001c0002t0014g0116 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.409-36878G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763688 | ||||||
| chr13:101763737
|
G | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-36927C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763737 | ||||||
| chr13:101763792
|
G | A | 2 | a0001c0001t0007g0081a0001c0001t0063g0090 | 2 | HG00280.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.409-36982C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763792 | ||||||
| chr13:101763811
|
G | A | 1 | a0001c0001t0100g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409-37001C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763811 | ||||||
| chr13:101763814
|
T | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-37004A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763814 | ||||||
| chr13:101763847
|
T | C | 11 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(8): Show | 11 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-37037A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763847 | ||||||
| chr13:101763897
|
C | T | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-37087G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101763897 | ||||||
| chr13:101764235
|
G | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-37425C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764235 | ||||||
| chr13:101764384
|
G | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-37574C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764384 | ||||||
| chr13:101764433
|
T | C | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-37623A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764433 | ||||||
| chr13:101764660
|
T | C | 5 | a0001c0001t0002g0055a0001c0001t0002g0098a0001c0001t0036g0061others(2): Show | 5 | HG03490.hp1 HG03492.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-37850A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764660 | ||||||
| chr13:101764671
|
G | A | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-37861C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764671 | ||||||
| chr13:101764688
|
C | T | 3 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.409-37878G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764688 | ||||||
| chr13:101764773
|
G | A | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-37963C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764773 | ||||||
| chr13:101764793
|
T | G | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.409-37983A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764793 | ||||||
| chr13:101764815
|
G | T | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-38005C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101764815 | ||||||
| chr13:101765045
|
G | C | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-38235C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765045 | ||||||
| chr13:101765054
|
T | C | 2 | a0001c0001t0057g0086a0001c0001t0105g0133 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-38244A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765054 | ||||||
| chr13:101765111
|
A | G | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.409-38301T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765111 | ||||||
| chr13:101765263
|
T | G | 81 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.409-38453A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765263 | ||||||
| chr13:101765440
|
A | G | 2 | a0001c0001t0003g0110a0001c0001t0110g0182 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.409-38630T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765440 | ||||||
| chr13:101765441
|
T | C | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-38631A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765441 | ||||||
| chr13:101765483
|
A | G | 1 | a0001c0001t0079g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.409-38673T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765483 | ||||||
| chr13:101765493
|
G | T | 2 | a0001c0001t0018g0221a0001c0001t0044g0178 | 2 | NA18969.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.409-38683C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765493 | ||||||
| chr13:101765544
|
G | A | 4 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-38734C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765544 | ||||||
| chr13:101765712
|
TTATTATT others(3): Show |
T | 15 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-38912_409-3890 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765712 | ||||||
| chr13:101765717
|
A | T | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-38907T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765717 | ||||||
| chr13:101765718
|
T | TTATTATT others(7): Show |
1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-38909_409-3890 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765718 | ||||||
| chr13:101765718
|
T | TTTTA | 4 | a0001c0001t0008g0208a0001c0001t0055g0006a0001c0001t0118g0242others(1): Show | 4 | HG01934.hp2 HG03195.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-38912_409-3890 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765718 | ||||||
| chr13:101765718
|
T | TTTTATTT others(13): Show |
1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-38928_409-3890 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765718 | ||||||
| chr13:101765785
|
A | G | 1 | a0001c0001t0007g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.409-38975T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765785 | ||||||
| chr13:101765799
|
G | A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-38989C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765799 | ||||||
| chr13:101765837
|
C | T | 10 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(7): Show | 10 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-39027G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765837 | ||||||
| chr13:101765953
|
T | C | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-39143A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765953 | ||||||
| chr13:101765999
|
G | A | 1 | a0001c0001t0030g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.409-39189C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101765999 | ||||||
| chr13:101766019
|
G | A | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-39209C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766019 | ||||||
| chr13:101766125
|
C | G | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-39315G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766125 | ||||||
| chr13:101766173
|
T | G | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-39363A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766173 | ||||||
| chr13:101766230
|
C | T | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-39420G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766230 | ||||||
| chr13:101766235
|
T | G | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-39425A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766235 | ||||||
| chr13:101766311
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-39501G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766311 | ||||||
| chr13:101766340
|
C | T | 1 | a0001c0001t0019g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.409-39530G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766340 | ||||||
| chr13:101766445
|
A | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-39635T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766445 | ||||||
| chr13:101766494
|
A | G | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-39684T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766494 | ||||||
| chr13:101766668
|
A | G | 253 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.409-39858T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766668 | ||||||
| chr13:101766708
|
A | C | 1 | a0001c0001t0034g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.409-39898T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766708 | ||||||
| chr13:101766758
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-39948A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766758 | ||||||
| chr13:101766868
|
T | C | 5 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-40058A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766868 | ||||||
| chr13:101766942
|
C | A | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-40132G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101766942 | ||||||
| chr13:101767126
|
T | C | 151 | a0001c0001t0001g0016a0001c0001t0002g0055a0001c0001t0002g0065others(148): Show | 151 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.409-40316A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767126 | ||||||
| chr13:101767351
|
C | G | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-40541G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767351 | ||||||
| chr13:101767372
|
A | C | 5 | a0001c0001t0047g0165a0001c0001t0047g0213a0001c0001t0091g0117others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-40562T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767372 | ||||||
| chr13:101767444
|
GAT | G | 4 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-40636_409-4063 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767444 | ||||||
| chr13:101767490
|
C | T | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-40680G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767490 | ||||||
| chr13:101767552
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.409-40742G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767552 | ||||||
| chr13:101767558
|
T | G | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-40748A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767558 | ||||||
| chr13:101767952
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-41142G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767952 | ||||||
| chr13:101767993
|
TG | T | 18 | a0001c0001t0001g0075a0001c0001t0006g0073a0001c0001t0006g0083others(15): Show | 18 | HG00099.hp2 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.409-41184delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101767993 | ||||||
| chr13:101768053
|
G | A | 2 | a0001c0001t0008g0233a0001c0001t0106g0163 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.409-41243C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768053 | ||||||
| chr13:101768292
|
T | G | 71 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.409-41482A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768292 | ||||||
| chr13:101768366
|
C | CT | 4 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-41557dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768366 | ||||||
| chr13:101768380
|
C | A | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-41570G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768380 | ||||||
| chr13:101768495
|
G | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-41685C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768495 | ||||||
| chr13:101768569
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-41759T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768569 | ||||||
| chr13:101768739
|
C | T | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-41929G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768739 | ||||||
| chr13:101768953
|
A | G | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.409-42143T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101768953 | ||||||
| chr13:101769029
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-42219T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769029 | ||||||
| chr13:101769040
|
G | A | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-42230C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769040 | ||||||
| chr13:101769061
|
T | C | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.409-42251A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769061 | ||||||
| chr13:101769190
|
T | C | 1 | a0001c0001t0011g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.409-42380A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769190 | ||||||
| chr13:101769354
|
T | TA | 140 | a0001c0001t0001g0016a0001c0001t0002g0055a0001c0001t0002g0065others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.409-42545dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769354 | ||||||
| chr13:101769417
|
T | C | 2 | a0001c0001t0093g0111a0001c0001t0113g0234 | 2 | HG01255.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.409-42607A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769417 | ||||||
| chr13:101769613
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-42803T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769613 | ||||||
| chr13:101769641
|
G | A | 247 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.409-42831C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769641 | ||||||
| chr13:101769715
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-42905G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769715 | ||||||
| chr13:101769736
|
C | T | 11 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(8): Show | 11 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-42926G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769736 | ||||||
| chr13:101769797
|
A | C | 236 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.409-42987T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769797 | ||||||
| chr13:101769831
|
A | C | 11 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(8): Show | 11 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-43021T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769831 | ||||||
| chr13:101769855
|
T | C | 1 | a0001c0001t0037g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.409-43045A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769855 | ||||||
| chr13:101769871
|
A | G | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-43061T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769871 | ||||||
| chr13:101769938
|
C | A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-43128G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769938 | ||||||
| chr13:101769973
|
G | A | 1 | a0001c0001t0027g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.409-43163C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769973 | ||||||
| chr13:101769975
|
A | G | 252 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.409-43165T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101769975 | ||||||
| chr13:101770118
|
G | A | 18 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0017g0135others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.409-43308C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770118 | ||||||
| chr13:101770127
|
TA | T | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-43318delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770127 | ||||||
| chr13:101770190
|
C | T | 247 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.409-43380G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770190 | ||||||
| chr13:101770228
|
G | A | 1 | a0001c0001t0064g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.409-43418C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770228 | ||||||
| chr13:101770329
|
G | A | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-43519C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770329 | ||||||
| chr13:101770509
|
T | G | 5 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-43699A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770509 | ||||||
| chr13:101770746
|
C | CA | 7 | a0001c0001t0047g0165a0001c0001t0047g0213a0001c0001t0057g0086others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-43937dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770746 | ||||||
| chr13:101770792
|
A | C | 265 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.409-43982T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770792 | ||||||
| chr13:101770807
|
A | G | 86 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-43997T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770807 | ||||||
| chr13:101770943
|
TAAAC | T | 7 | a0001c0001t0009g0159a0001c0001t0009g0241a0001c0001t0045g0214others(4): Show | 7 | HG02622.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-44137_409-4413 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770943 | ||||||
| chr13:101770981
|
C | G | 2 | a0001c0001t0001g0051a0001c0001t0011g0223 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.409-44171G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101770981 | ||||||
| chr13:101771126
|
G | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-44316C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771126 | ||||||
| chr13:101771295
|
T | C | 1 | a0001c0001t0008g0208 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.409-44485A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771295 | ||||||
| chr13:101771302
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.409-44492T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771302 | ||||||
| chr13:101771352
|
G | A | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-44542C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771352 | ||||||
| chr13:101771374
|
C | G | 15 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-44564G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771374 | ||||||
| chr13:101771375
|
ACC | A | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-44567_409-4456 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771375 | ||||||
| chr13:101771640
|
A | C | 1 | a0001c0001t0072g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.409-44830T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101771640 | ||||||
| chr13:101772069
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0093g0111others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-45259A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772069 | ||||||
| chr13:101772072
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.409-45262A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772072 | ||||||
| chr13:101772085
|
A | T | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-45275T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772085 | ||||||
| chr13:101772310
|
C | T | 1 | a0001c0001t0078g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.409-45500G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772310 | ||||||
| chr13:101772331
|
G | C | 2 | a0001c0001t0051g0002a0001c0001t0061g0025 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-45521C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772331 | ||||||
| chr13:101772408
|
TTAAAC | T | 22 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0021g0170others(19): Show | 22 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.409-45603_409-4559 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772408 | ||||||
| chr13:101772557
|
C | T | 1 | a0001c0001t0080g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.409-45747G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772557 | ||||||
| chr13:101772641
|
C | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-45831G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772641 | ||||||
| chr13:101772650
|
G | C | 5 | a0001c0001t0015g0114a0001c0001t0051g0002a0001c0001t0061g0025others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-45840C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772650 | ||||||
| chr13:101772686
|
A | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-45876T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772686 | ||||||
| chr13:101772746
|
G | A | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-45936C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772746 | ||||||
| chr13:101772855
|
A | G | 5 | a0001c0001t0002g0055a0001c0001t0002g0098a0001c0001t0036g0061others(2): Show | 5 | HG03490.hp1 HG03492.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-46045T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772855 | ||||||
| chr13:101772872
|
C | T | 247 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.409-46062G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772872 | ||||||
| chr13:101772925
|
A | G | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-46115T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101772925 | ||||||
| chr13:101773025
|
G | A | 1 | a0001c0001t0044g0252 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.409-46215C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773025 | ||||||
| chr13:101773329
|
A | G | 11 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(8): Show | 11 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-46519T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773329 | ||||||
| chr13:101773360
|
C | T | 1 | a0001c0001t0030g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.409-46550G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773360 | ||||||
| chr13:101773410
|
AT | A | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-46601delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773410 | ||||||
| chr13:101773416
|
T | C | 1 | a0001c0001t0046g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.409-46606A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773416 | ||||||
| chr13:101773501
|
A | G | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-46691T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773501 | ||||||
| chr13:101773562
|
A | G | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-46752T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773562 | ||||||
| chr13:101773569
|
A | G | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.409-46759T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773569 | ||||||
| chr13:101773578
|
A | G | 1 | a0001c0001t0152g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.409-46768T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773578 | ||||||
| chr13:101773641
|
A | G | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-46831T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773641 | ||||||
| chr13:101773816
|
G | C | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-47006C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773816 | ||||||
| chr13:101773893
|
C | T | 2 | a0001c0001t0006g0083a0001c0001t0006g0085 | 2 | HG01099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.409-47083G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773893 | ||||||
| chr13:101773937
|
T | C | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-47127A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773937 | ||||||
| chr13:101773981
|
T | G | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.409-47171A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101773981 | ||||||
| chr13:101774038
|
A | G | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.409-47228T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774038 | ||||||
| chr13:101774225
|
T | C | 1 | a0001c0001t0012g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.409-47415A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774225 | ||||||
| chr13:101774263
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-47453C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774263 | ||||||
| chr13:101774347
|
C | G | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-47537G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774347 | ||||||
| chr13:101774376
|
G | C | 1 | a0001c0001t0079g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.409-47566C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774376 | ||||||
| chr13:101774443
|
C | T | 1 | a0001c0001t0038g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.409-47633G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774443 | ||||||
| chr13:101774509
|
C | T | 1 | a0001c0001t0134g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.409-47699G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774509 | ||||||
| chr13:101774515
|
G | A | 86 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-47705C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774515 | ||||||
| chr13:101774607
|
T | C | 2 | a0001c0001t0037g0066a0001c0001t0038g0125 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.409-47797A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774607 | ||||||
| chr13:101774677
|
G | A | 2 | a0001c0001t0027g0026a0001c0001t0027g0046 | 2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.409-47867C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774677 | ||||||
| chr13:101774772
|
G | A | 2 | a0001c0001t0007g0037a0001c0001t0007g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.409-47962C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774772 | ||||||
| chr13:101774968
|
T | C | 1 | a0001c0001t0030g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.409-48158A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774968 | ||||||
| chr13:101774969
|
C | CA | 12 | a0001c0001t0009g0241a0001c0001t0017g0139a0001c0001t0045g0214others(9): Show | 12 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-48160dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774969 | ||||||
| chr13:101774969
|
CA | C | 6 | a0001c0001t0015g0114a0001c0001t0023g0158a0001c0001t0089g0017others(3): Show | 6 | HG01891.hp1 HG01943.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-48160delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774969 | ||||||
| chr13:101774987
|
A | G | 2 | a0001c0001t0007g0042a0001c0001t0007g0043 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.409-48177T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101774987 | ||||||
| chr13:101775184
|
C | T | 101 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(98): Show | 101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.409-48374G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775184 | ||||||
| chr13:101775294
|
C | T | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.409-48484G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775294 | ||||||
| chr13:101775523
|
AGT | A | 95 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.409-48715_409-4871 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775523 | ||||||
| chr13:101775730
|
T | C | 6 | a0001c0001t0009g0159a0001c0001t0015g0114a0001c0001t0051g0002others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-48920A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775730 | ||||||
| chr13:101775748
|
G | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-48938C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775748 | ||||||
| chr13:101775855
|
T | C | 15 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-49045A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775855 | ||||||
| chr13:101775856
|
C | G | 6 | a0001c0001t0009g0241a0001c0001t0045g0214a0001c0001t0045g0215others(3): Show | 6 | HG02622.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-49046G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775856 | ||||||
| chr13:101775900
|
T | G | 2 | a0001c0001t0023g0157a0001c0001t0023g0158 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-49090A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101775900 | ||||||
| chr13:101776074
|
G | A | 110 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.409-49264C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776074 | ||||||
| chr13:101776076
|
T | C | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-49266A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776076 | ||||||
| chr13:101776079
|
C | T | 110 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.409-49269G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776079 | ||||||
| chr13:101776102
|
C | A | 221 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.409-49292G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776102 | ||||||
| chr13:101776142
|
C | T | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-49332G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776142 | ||||||
| chr13:101776226
|
C | A | 1 | a0001c0001t0095g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.409-49416G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776226 | ||||||
| chr13:101776262
|
A | G | 1 | a0001c0001t0011g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.409-49452T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776262 | ||||||
| chr13:101776637
|
G | C | 252 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.409-49827C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101776637 | ||||||
| chr13:101777063
|
C | T | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-50253G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777063 | ||||||
| chr13:101777109
|
T | G | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-50299A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777109 | ||||||
| chr13:101777156
|
G | A | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-50346C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777156 | ||||||
| chr13:101777180
|
T | C | 1 | a0001c0001t0003g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.409-50370A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777180 | ||||||
| chr13:101777315
|
G | A | 114 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(111): Show | 114 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.409-50505C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777315 | ||||||
| chr13:101777322
|
G | C | 2 | a0001c0001t0013g0142a0001c0001t0094g0119 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.409-50512C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777322 | ||||||
| chr13:101777352
|
G | A | 1 | a0001c0001t0059g0034 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.409-50542C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777352 | ||||||
| chr13:101777494
|
A | G | 113 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.409-50684T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777494 | ||||||
| chr13:101777496
|
A | G | 1 | a0001c0001t0011g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.409-50686T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777496 | ||||||
| chr13:101777727
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(7): Show | 10 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-50917G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777727 | ||||||
| chr13:101777734
|
G | T | 15 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-50924C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777734 | ||||||
| chr13:101777879
|
G | T | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-51069C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777879 | ||||||
| chr13:101777913
|
G | A | 112 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.409-51103C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101777913 | ||||||
| chr13:101778113
|
G | A | 233 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.409-51303C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778113 | ||||||
| chr13:101778256
|
C | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-51446G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778256 | ||||||
| chr13:101778303
|
C | A | 71 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.409-51493G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778303 | ||||||
| chr13:101778342
|
G | A | 1 | a0001c0001t0149g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.409-51532C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778342 | ||||||
| chr13:101778361
|
C | CCATCATG others(3): Show |
1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-51561_409-5155 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778361 | ||||||
| chr13:101778390
|
G | A | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-51580C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778390 | ||||||
| chr13:101778490
|
G | C | 2 | a0001c0001t0015g0114a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.409-51680C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778490 | ||||||
| chr13:101778558
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(8): Show | 11 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-51748G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778558 | ||||||
| chr13:101778623
|
CATTCTCA | C | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-51820_409-5181 others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778623 | ||||||
| chr13:101778683
|
C | T | 16 | a0001c0001t0010g0153a0001c0001t0010g0248a0001c0001t0010g0249others(13): Show | 16 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.409-51873G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778683 | ||||||
| chr13:101778685
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0084g0040a0001c0001t0135g0183 | 3 | HG01257.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.409-51875G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778685 | ||||||
| chr13:101778686
|
G | T | 111 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.409-51876C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778686 | ||||||
| chr13:101778766
|
T | C | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-51956A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778766 | ||||||
| chr13:101778814
|
G | A | 252 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.409-52004C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778814 | ||||||
| chr13:101778863
|
GA | G | 112 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.409-52054delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101778863 | ||||||
| chr13:101779001
|
G | C | 112 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.409-52191C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779001 | ||||||
| chr13:101779120
|
T | C | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409-52310A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779120 | ||||||
| chr13:101779212
|
C | T | 3 | a0001c0001t0081g0120a0001c0001t0130g0219a0001c0001t0159g0257 | 3 | HG01884.hp2 HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.409-52402G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779212 | ||||||
| chr13:101779222
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-52412G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779222 | ||||||
| chr13:101779412
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-52602A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779412 | ||||||
| chr13:101779460
|
A | C | 2 | a0001c0001t0049g0218a0001c0001t0103g0134 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.409-52650T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779460 | ||||||
| chr13:101779606
|
A | G | 1 | a0001c0001t0019g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.409-52796T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779606 | ||||||
| chr13:101779754
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-52944A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779754 | ||||||
| chr13:101779810
|
G | C | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-53000C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101779810 | ||||||
| chr13:101780336
|
C | A | 1 | a0001c0001t0009g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.409-53526G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780336 | ||||||
| chr13:101780383
|
C | T | 1 | a0001c0001t0136g0204 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.409-53573G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780383 | ||||||
| chr13:101780490
|
C | T | 2 | a0001c0001t0057g0086a0001c0001t0118g0242 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.409-53680G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780490 | ||||||
| chr13:101780594
|
T | C | 1 | a0001c0001t0094g0119 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.409-53784A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780594 | ||||||
| chr13:101780693
|
A | G | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-53883T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780693 | ||||||
| chr13:101780721
|
C | T | 1 | a0001c0001t0078g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.409-53911G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780721 | ||||||
| chr13:101780768
|
A | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-53958T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780768 | ||||||
| chr13:101780971
|
T | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-54161A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101780971 | ||||||
| chr13:101781049
|
G | T | 1 | a0001c0001t0002g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.409-54239C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781049 | ||||||
| chr13:101781117
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-54307G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781117 | ||||||
| chr13:101781136
|
GTCTCTC | G | 127 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.409-54332_409-5432 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781136 | ||||||
| chr13:101781150
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-54340G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781150 | ||||||
| chr13:101781229
|
T | A | 235 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.409-54419A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781229 | ||||||
| chr13:101781643
|
T | G | 85 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-54833A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781643 | ||||||
| chr13:101781748
|
G | T | 2 | a0001c0001t0007g0037a0001c0001t0007g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.409-54938C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781748 | ||||||
| chr13:101781901
|
G | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-55091C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781901 | ||||||
| chr13:101781922
|
C | T | 2 | a0001c0001t0037g0066a0001c0001t0038g0125 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.409-55112G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781922 | ||||||
| chr13:101781993
|
T | C | 126 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(123): Show | 126 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.409-55183A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101781993 | ||||||
| chr13:101782006
|
T | A | 1 | a0001c0001t0129g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.409-55196A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782006 | ||||||
| chr13:101782216
|
TATTTA | T | 6 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-55411_409-5540 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782216 | ||||||
| chr13:101782453
|
G | C | 2 | a0001c0001t0057g0086a0001c0001t0151g0147 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-55643C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782453 | ||||||
| chr13:101782457
|
T | G | 5 | a0001c0001t0009g0159a0001c0001t0047g0165a0001c0001t0091g0117others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-55647A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782457 | ||||||
| chr13:101782579
|
C | A | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.409-55769G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782579 | ||||||
| chr13:101782853
|
T | C | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.409-56043A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101782853 | ||||||
| chr13:101783030
|
C | G | 1 | a0001c0001t0148g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.409-56220G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783030 | ||||||
| chr13:101783109
|
G | GCATTTCT others(9): Show |
1 | a0001c0001t0041g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.409-56315_409-5630 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783109 | ||||||
| chr13:101783198
|
G | A | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.409-56388C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783198 | ||||||
| chr13:101783211
|
C | T | 1 | a0001c0001t0086g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.409-56401G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783211 | ||||||
| chr13:101783243
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-56433C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783243 | ||||||
| chr13:101783385
|
G | A | 2 | a0001c0001t0057g0086a0001c0001t0151g0147 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.409-56575C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783385 | ||||||
| chr13:101783468
|
C | CA | 88 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.409-56659dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783468 | ||||||
| chr13:101783648
|
C | A | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.409-56838G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783648 | ||||||
| chr13:101783785
|
G | A | 10 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0019g0227others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-56975C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783785 | ||||||
| chr13:101783872
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0098 | 2 | NA18986.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.409-57062C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783872 | ||||||
| chr13:101783898
|
C | G | 1 | a0001c0001t0094g0119 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.409-57088G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783898 | ||||||
| chr13:101783990
|
G | A | 1 | a0001c0001t0031g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.409-57180C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101783990 | ||||||
| chr13:101784288
|
C | A | 3 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.409-57478G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784288 | ||||||
| chr13:101784341
|
G | A | 2 | a0001c0001t0092g0113a0001c0001t0113g0234 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.409-57531C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784341 | ||||||
| chr13:101784622
|
A | G | 1 | a0001c0001t0155g0149 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.409-57812T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784622 | ||||||
| chr13:101784745
|
T | A | 3 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0090g0015 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-57935A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784745 | ||||||
| chr13:101784752
|
G | T | 245 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.409-57942C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784752 | ||||||
| chr13:101784764
|
G | A | 5 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0004g0078others(2): Show | 5 | HG01496.hp1 HG01928.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-57954C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784764 | ||||||
| chr13:101784845
|
A | G | 10 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0019g0227others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-58035T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101784845 | ||||||
| chr13:101785063
|
G | T | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-58253C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785063 | ||||||
| chr13:101785183
|
T | C | 1 | a0001c0001t0115g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.409-58373A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785183 | ||||||
| chr13:101785218
|
T | C | 1 | a0001c0001t0060g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.409-58408A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785218 | ||||||
| chr13:101785269
|
C | T | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-58459G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785269 | ||||||
| chr13:101785352
|
TA | T | 115 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(112): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.409-58543delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785352 | ||||||
| chr13:101785479
|
A | T | 17 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(14): Show | 17 | HG01255.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.409-58669T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785479 | ||||||
| chr13:101785594
|
G | A | 121 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.409-58784C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785594 | ||||||
| chr13:101785625
|
A | T | 264 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.409-58815T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785625 | ||||||
| chr13:101785638
|
T | A | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.409-58828A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785638 | ||||||
| chr13:101785696
|
T | C | 1 | a0001c0001t0006g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.409-58886A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785696 | ||||||
| chr13:101785900
|
A | G | 124 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.409-59090T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785900 | ||||||
| chr13:101785970
|
A | G | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.409-59160T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101785970 | ||||||
| chr13:101786295
|
A | G | 2 | a0001c0001t0007g0081a0001c0001t0063g0090 | 2 | HG00280.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.409-59485T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786295 | ||||||
| chr13:101786307
|
T | A | 1 | a0001c0001t0020g0187 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.409-59497A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786307 | ||||||
| chr13:101786351
|
A | G | 122 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.409-59541T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786351 | ||||||
| chr13:101786397
|
T | A | 3 | a0001c0001t0034g0038a0001c0001t0034g0054a0001c0001t0059g0034 | 3 | HG00099.hp2 HG01255.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.409-59587A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786397 | ||||||
| chr13:101786481
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(3): Show | 6 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-59671C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786481 | ||||||
| chr13:101786488
|
G | A | 17 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(14): Show | 17 | HG01255.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.409-59678C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786488 | ||||||
| chr13:101786641
|
C | T | 6 | a0001c0001t0017g0139a0001c0001t0051g0002a0001c0001t0061g0025others(3): Show | 6 | HG01884.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-59831G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786641 | ||||||
| chr13:101786787
|
A | G | 41 | a0001c0001t0002g0055a0001c0001t0002g0065a0001c0001t0002g0096others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.409-59977T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786787 | ||||||
| chr13:101786789
|
A | T | 233 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.409-59979T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786789 | ||||||
| chr13:101786833
|
A | G | 77 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.409-60023T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786833 | ||||||
| chr13:101786911
|
T | A | 1 | a0001c0001t0142g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.409-60101A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786911 | ||||||
| chr13:101786928
|
C | G | 232 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.409-60118G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101786928 | ||||||
| chr13:101787072
|
T | G | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.409-60262A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787072 | ||||||
| chr13:101787180
|
T | TC | 233 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.409-60371dupG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787180 | ||||||
| chr13:101787187
|
C | T | 1 | a0001c0001t0106g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.409-60377G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787187 | ||||||
| chr13:101787223
|
T | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-60413A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787223 | ||||||
| chr13:101787313
|
G | T | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.409-60503C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787313 | ||||||
| chr13:101787576
|
A | G | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.409-60766T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787576 | ||||||
| chr13:101787637
|
T | C | 3 | a0001c0001t0015g0114a0001c0001t0089g0017a0001c0001t0095g0022 | 3 | HG01891.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.409-60827A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787637 | ||||||
| chr13:101787707
|
A | G | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.409-60897T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787707 | ||||||
| chr13:101787775
|
C | T | 2 | a0001c0001t0029g0099a0001c0001t0039g0185 | 2 | NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.409-60965G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787775 | ||||||
| chr13:101787897
|
G | A | 1 | a0001c0001t0055g0006 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.409-61087C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101787897 | ||||||
| chr13:101788018
|
T | C | 4 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-61208A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788018 | ||||||
| chr13:101788085
|
C | T | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-61275G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788085 | ||||||
| chr13:101788245
|
C | G | 207 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.409-61435G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788245 | ||||||
| chr13:101788290
|
C | A | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-61480G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788290 | ||||||
| chr13:101788352
|
G | C | 3 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.409-61542C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788352 | ||||||
| chr13:101788431
|
C | G | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-61621G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788431 | ||||||
| chr13:101788459
|
A | C | 3 | a0001c0001t0001g0127a0001c0001t0007g0081a0001c0001t0063g0090 | 3 | HG00280.hp2 HG01928.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.409-61649T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788459 | ||||||
| chr13:101788490
|
G | A | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.409-61680C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788490 | ||||||
| chr13:101788533
|
C | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112 | 3 | HG03209.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.409-61723G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788533 | ||||||
| chr13:101788584
|
C | G | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-61774G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788584 | ||||||
| chr13:101788872
|
C | CTA | 4 | a0001c0001t0001g0029a0001c0001t0108g0172a0001c0001t0150g0146others(1): Show | 4 | HG02055.hp1 HG02145.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-62064_409-6206 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATA | 3 | a0001c0001t0010g0201a0001c0001t0011g0190a0001c0001t0138g0222 | 3 | HG00597.hp1 HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.409-62066_409-6206 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATATA | 4 | a0001c0001t0008g0151a0001c0001t0035g0044a0001c0001t0065g0080others(1): Show | 4 | HG01433.hp2 HG01978.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-62068_409-6206 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATATAT others(1): Show |
3 | a0001c0001t0018g0236a0001c0001t0067g0091a0001c0001t0068g0009 | 3 | HG04228.hp2 NA19084.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.409-62070_409-6206 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0081g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.409-62072_409-6206 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0027g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.409-62074_409-6206 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0140g0192 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.409-62078_409-6206 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
CTA | C | 3 | a0001c0001t0043g0253a0001c0001t0064g0126a0001c0001t0147g0220 | 3 | HG03688.hp1 NA19043.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.409-62064_409-6206 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
CTATA | C | 4 | a0001c0001t0006g0083a0001c0001t0008g0173a0001c0001t0038g0064others(1): Show | 4 | HG01516.hp1 HG02257.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-62066_409-6206 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788872
|
CTATATA | C | 3 | a0001c0001t0004g0071a0001c0001t0027g0046a0001c0001t0131g0162 | 3 | HG02273.hp1 HG03225.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.409-62068_409-6206 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788872 | ||||||
| chr13:101788893
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0033g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.409-62109_409-6208 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788893 | ||||||
| chr13:101788895
|
TATATATA others(17): Show |
T | 5 | a0001c0001t0013g0144a0001c0001t0013g0212a0001c0001t0049g0141others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-62109_409-6208 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788895 | ||||||
| chr13:101788895
|
TATATATA others(21): Show |
T | 1 | a0001c0001t0025g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.409-62113_409-6208 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788895 | ||||||
| chr13:101788895
|
TATATATA others(27): Show |
T | 1 | a0001c0001t0145g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.409-62119_409-6208 others(38): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788895 | ||||||
| chr13:101788897
|
TATATATA others(17): Show |
T | 6 | a0001c0001t0009g0203a0001c0001t0013g0142a0001c0001t0016g0130others(3): Show | 6 | HG00423.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-62111_409-6208 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788897 | ||||||
| chr13:101788897
|
TATATATA others(23): Show |
T | 2 | a0001c0001t0032g0039a0001c0001t0132g0184 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.409-62117_409-6208 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788897 | ||||||
| chr13:101788899
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.409-62107_409-6209 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0021g0225a0001c0001t0089g0017 | 2 | HG01891.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.409-62111_409-6209 others(26): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(17): Show |
T | 6 | a0001c0001t0002g0104a0001c0001t0003g0030a0001c0001t0004g0088others(3): Show | 6 | HG01109.hp2 HG02145.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-62113_409-6209 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(19): Show |
T | 3 | a0001c0001t0038g0125a0001c0001t0040g0188a0001c0001t0040g0189 | 3 | HG02738.hp1 NA18948.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.409-62115_409-6209 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(21): Show |
T | 3 | a0001c0001t0055g0006a0001c0001t0107g0175a0001c0001t0114g0186 | 3 | HG00280.hp1 HG02135.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.409-62117_409-6209 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(23): Show |
T | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.409-62119_409-6209 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(27): Show |
T | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.409-62123_409-6209 others(38): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788899
|
TATATATA others(33): Show |
T | 2 | a0001c0001t0047g0165a0001c0001t0154g0145 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.409-62129_409-6209 others(44): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788899 | ||||||
| chr13:101788901
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0066g0112a0001c0001t0097g0020a0001c0001t0099g0011 | 3 | HG02622.hp1 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.409-62101_409-6209 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0011g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.409-62105_409-6209 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0120g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.409-62109_409-6209 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(13): Show |
T | 3 | a0001c0001t0012g0216a0001c0001t0015g0121a0001c0001t0139g0181 | 3 | HG01516.hp2 HG01934.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.409-62111_409-6209 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0035g0089a0001c0001t0042g0205 | 2 | HG02074.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.409-62113_409-6209 others(26): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(17): Show |
T | 6 | a0001c0001t0016g0010a0001c0001t0023g0164a0001c0001t0026g0123others(3): Show | 6 | HG01169.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-62115_409-6209 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(19): Show |
T | 2 | a0001c0001t0031g0035a0001c0001t0037g0066 | 2 | HG01257.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.409-62117_409-6209 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(21): Show |
T | 2 | a0001c0001t0033g0049a0001c0001t0049g0218 | 2 | HG02074.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.409-62119_409-6209 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(23): Show |
T | 2 | a0001c0001t0001g0016a0001c0001t0032g0060 | 2 | HG01433.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.409-62121_409-6209 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788901
|
TATATATA others(33): Show |
T | 2 | a0001c0001t0091g0117a0001c0002t0014g0116 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.409-62131_409-6209 others(44): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788901 | ||||||
| chr13:101788903
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-62103_409-6209 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0001g0075a0001c0001t0006g0073 | 2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.409-62109_409-6209 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0004g0070a0001c0001t0011g0150 | 2 | HG01496.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.409-62111_409-6209 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0009g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.409-62117_409-6209 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(19): Show |
T | 4 | a0001c0001t0050g0001a0001c0001t0109g0199a0001c0001t0143g0239others(1): Show | 4 | HG01099.hp1 HG03098.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-62119_409-6209 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(21): Show |
T | 4 | a0001c0001t0010g0249a0001c0001t0044g0252a0001c0001t0069g0024others(1): Show | 4 | HG00423.hp1 HG04199.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-62121_409-6209 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788903
|
TATATATA others(23): Show |
T | 3 | a0001c0001t0008g0152a0001c0001t0053g0005a0001c0001t0122g0193 | 3 | HG00323.hp2 HG01106.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.409-62123_409-6209 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788903 | ||||||
| chr13:101788905
|
T | G | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.409-62095A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAG | T | 5 | a0001c0001t0002g0109a0001c0001t0004g0078a0001c0001t0026g0027others(2): Show | 5 | HG01256.hp1 HG01975.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-62101_409-6209 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(1): Show |
T | 6 | a0001c0001t0002g0101a0001c0001t0003g0110a0001c0001t0009g0159others(3): Show | 6 | HG00408.hp1 HG02258.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-62103_409-6209 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(3): Show |
T | 5 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0045g0214others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-62105_409-6209 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(5): Show |
T | 5 | a0001c0001t0003g0031a0001c0001t0019g0227a0001c0001t0034g0054others(2): Show | 5 | HG00099.hp2 HG02135.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-62107_409-6209 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(9): Show |
T | 2 | a0001c0001t0003g0058a0001c0001t0006g0085 | 2 | HG01099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.409-62111_409-6209 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(17): Show |
T | 2 | a0001c0001t0070g0028a0001c0001t0137g0240 | 2 | HG00642.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.409-62119_409-6209 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(19): Show |
T | 2 | a0001c0001t0010g0153a0001c0001t0017g0135 | 2 | HG01081.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.409-62121_409-6209 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(21): Show |
T | 2 | a0001c0001t0012g0191a0001c0001t0103g0134 | 2 | HG03453.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.409-62123_409-6209 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788905
|
TATATAGA others(23): Show |
T | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.409-62125_409-6209 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788905 | ||||||
| chr13:101788907
|
T | G | 2 | a0001c0001t0064g0126a0001c0001t0147g0220 | 2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.409-62097A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(5): Show |
T | 4 | a0001c0001t0009g0241a0001c0001t0041g0226a0001c0001t0121g0160others(1): Show | 4 | HG00597.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-62109_409-6209 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(7): Show |
T | 1 | a0001c0001t0034g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.409-62111_409-6209 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(17): Show |
T | 2 | a0001c0001t0142g0228a0001c0002t0128g0155 | 2 | NA18906.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.409-62121_409-6209 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(19): Show |
T | 1 | a0001c0001t0010g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.409-62123_409-6209 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(21): Show |
T | 1 | a0001c0001t0046g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.409-62125_409-6209 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(23): Show |
T | 1 | a0001c0001t0025g0007 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.409-62127_409-6209 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788907
|
TATAGAGA others(25): Show |
T | 1 | a0001c0001t0030g0032 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.409-62129_409-6209 others(36): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788907 | ||||||
| chr13:101788909
|
T | G | 5 | a0001c0001t0001g0033a0001c0001t0043g0253a0001c0001t0064g0126others(2): Show | 5 | HG03225.hp1 HG03688.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-62099A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788909 | ||||||
| chr13:101788909
|
T | TATATATA others(3): Show |
1 | a0001c0001t0006g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.409-62100_409-6209 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788909 | ||||||
| chr13:101788909
|
TAG | T | 5 | a0001c0001t0019g0244a0001c0001t0080g0021a0001c0001t0082g0072others(2): Show | 5 | HG01975.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-62101_409-6210 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788909 | ||||||
| chr13:101788909
|
TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.409-62109_409-6210 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788909 | ||||||
| chr13:101788911
|
G | T | 97 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(94): Show | 97 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.409-62101C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788911 | ||||||
| chr13:101788913
|
G | T | 85 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.409-62103C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788913 | ||||||
| chr13:101788915
|
G | T | 64 | a0001c0001t0001g0093a0001c0001t0001g0127a0001c0001t0002g0065others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.409-62105C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788915 | ||||||
| chr13:101788917
|
G | T | 46 | a0001c0001t0001g0127a0001c0001t0003g0106a0001c0001t0004g0057others(43): Show | 46 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.409-62107C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788917 | ||||||
| chr13:101788919
|
G | T | 27 | a0001c0001t0001g0127a0001c0001t0003g0106a0001c0001t0004g0057others(24): Show | 27 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.409-62109C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788919 | ||||||
| chr13:101788921
|
G | T | 12 | a0001c0001t0001g0127a0001c0001t0023g0157a0001c0001t0023g0158others(9): Show | 12 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.409-62111C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788921 | ||||||
| chr13:101788921
|
GAGAGAGA others(21): Show |
G | 1 | a0001c0001t0124g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.409-62139_409-6211 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788921 | ||||||
| chr13:101788923
|
G | T | 5 | a0001c0001t0001g0127a0001c0001t0052g0003a0001c0001t0056g0107others(2): Show | 5 | HG00438.hp1 HG00438.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-62113C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788923 | ||||||
| chr13:101788925
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0108g0172 | 2 | HG03654.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.409-62115C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788925 | ||||||
| chr13:101788925
|
GAGAGAGA others(17): Show |
G | 3 | a0001c0001t0012g0230a0001c0002t0014g0118a0001c0002t0127g0224 | 3 | HG01192.hp2 HG02071.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.409-62139_409-6211 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788925 | ||||||
| chr13:101788929
|
GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0100g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409-62139_409-6212 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788929 | ||||||
| chr13:101788931
|
GAGAGAGA others(11): Show |
G | 4 | a0001c0001t0003g0076a0001c0001t0062g0056a0001c0001t0116g0246others(1): Show | 4 | HG01943.hp1 HG01943.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-62139_409-6212 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788931 | ||||||
| chr13:101788933
|
GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0005g0102a0001c0001t0054g0004a0001c0001t0111g0202 | 3 | HG00621.hp2 NA18986.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.409-62139_409-6212 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788933 | ||||||
| chr13:101788935
|
GAGAGAGA others(7): Show |
G | 6 | a0001c0001t0048g0168a0001c0001t0059g0034a0001c0001t0071g0128others(3): Show | 6 | HG01175.hp1 HG01255.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-62139_409-6212 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788935 | ||||||
| chr13:101788937
|
GAGAGAGA others(5): Show |
G | 11 | a0001c0001t0002g0065a0001c0001t0004g0057a0001c0001t0005g0047others(8): Show | 11 | HG00621.hp1 HG01074.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-62139_409-6212 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788937 | ||||||
| chr13:101788939
|
GAGAGAGA others(3): Show |
G | 6 | a0001c0001t0002g0096a0001c0001t0005g0048a0001c0001t0005g0067others(3): Show | 6 | HG02698.hp1 HG03491.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-62139_409-6213 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788939 | ||||||
| chr13:101788941
|
GAGAGAGA others(1): Show |
G | 7 | a0001c0001t0001g0051a0001c0001t0002g0055a0001c0001t0003g0106others(4): Show | 7 | HG01169.hp1 HG01993.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-62139_409-6213 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788941 | ||||||
| chr13:101788943
|
GAGAGAC | G | 13 | a0001c0001t0007g0042a0001c0001t0007g0081a0001c0001t0011g0223others(10): Show | 13 | HG00280.hp2 HG00544.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-62139_409-6213 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788943 | ||||||
| chr13:101788945
|
GAGAC | G | 15 | a0001c0001t0001g0036a0001c0001t0007g0037a0001c0001t0007g0052others(12): Show | 15 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-62139_409-6213 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788945 | ||||||
| chr13:101788947
|
GAC | G | 6 | a0001c0001t0002g0098a0001c0001t0022g0194a0001c0001t0115g0176others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-62139_409-6213 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788947 | ||||||
| chr13:101788949
|
C | G | 126 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.409-62139G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788949 | ||||||
| chr13:101788949
|
CAGAGAGA others(3): Show |
C | 2 | a0001c0001t0009g0159a0001c0001t0051g0002 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.409-62149_409-6214 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788949 | ||||||
| chr13:101788949
|
CAGAGAGA others(7): Show |
C | 20 | a0001c0001t0002g0101a0001c0001t0002g0109a0001c0001t0004g0071others(17): Show | 20 | HG00099.hp1 HG00408.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.409-62153_409-6214 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788949 | ||||||
| chr13:101788949
|
CAGAGAGA others(9): Show |
C | 8 | a0001c0001t0006g0083a0001c0001t0008g0173a0001c0001t0044g0178others(5): Show | 8 | HG01109.hp1 HG01192.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.409-62155_409-6214 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788949 | ||||||
| chr13:101788955
|
G | C | 16 | a0001c0001t0010g0153a0001c0001t0013g0142a0001c0001t0013g0143others(13): Show | 16 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-62145C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788955 | ||||||
| chr13:101788959
|
G | C | 6 | a0001c0001t0016g0012a0001c0001t0017g0139a0001c0001t0105g0133others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.409-62149C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788959 | ||||||
| chr13:101788963
|
G | C | 103 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(100): Show | 103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.409-62153C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788963 | ||||||
| chr13:101788965
|
G | C | 65 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.409-62155C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101788965 | ||||||
| chr13:101789216
|
C | T | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-62406G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789216 | ||||||
| chr13:101789259
|
C | G | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.409-62449G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789259 | ||||||
| chr13:101789319
|
C | T | 91 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.409-62509G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789319 | ||||||
| chr13:101789345
|
A | G | 130 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.409-62535T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789345 | ||||||
| chr13:101789604
|
A | G | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-62794T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789604 | ||||||
| chr13:101789632
|
G | T | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-62822C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789632 | ||||||
| chr13:101789842
|
T | G | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.409-63032A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789842 | ||||||
| chr13:101789846
|
TCAGA | T | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-63040_409-6303 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789846 | ||||||
| chr13:101789900
|
C | T | 15 | a0001c0001t0009g0159a0001c0001t0021g0170a0001c0001t0023g0157others(12): Show | 15 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-63090G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789900 | ||||||
| chr13:101789987
|
T | C | 7 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(4): Show | 7 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-63177A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101789987 | ||||||
| chr13:101790126
|
TG | T | 87 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.409-63317delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790126 | ||||||
| chr13:101790128
|
G | GTT | 8 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0009g0159others(5): Show | 8 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.409-63320_409-6331 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790128 | ||||||
| chr13:101790128
|
GT | G | 133 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.409-63319delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790128 | ||||||
| chr13:101790199
|
ACTT | A | 7 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(4): Show | 7 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-63392_409-6339 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790199 | ||||||
| chr13:101790255
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0098 | 2 | NA18986.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.409-63445T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790255 | ||||||
| chr13:101790268
|
T | C | 1 | a0001c0001t0005g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.409-63458A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790268 | ||||||
| chr13:101790297
|
G | A | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.409-63487C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790297 | ||||||
| chr13:101790372
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-63562C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790372 | ||||||
| chr13:101790409
|
C | CT | 76 | a0001c0001t0002g0101a0001c0001t0002g0104a0001c0001t0002g0109others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.409-63600dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790409 | ||||||
| chr13:101790409
|
CTTT | C | 92 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.409-63602_409-6360 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790409 | ||||||
| chr13:101790718
|
G | A | 93 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.409-63908C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790718 | ||||||
| chr13:101790893
|
G | A | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-64083C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790893 | ||||||
| chr13:101790922
|
C | T | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-64112G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790922 | ||||||
| chr13:101790968
|
C | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-64158G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101790968 | ||||||
| chr13:101791048
|
A | G | 93 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.409-64238T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791048 | ||||||
| chr13:101791066
|
TG | T | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-64257delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791066 | ||||||
| chr13:101791345
|
A | G | 93 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.409-64535T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791345 | ||||||
| chr13:101791377
|
C | G | 1 | a0001c0001t0009g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.409-64567G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791377 | ||||||
| chr13:101791401
|
G | A | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.409-64591C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791401 | ||||||
| chr13:101791408
|
T | C | 246 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.409-64598A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791408 | ||||||
| chr13:101791573
|
C | T | 109 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.409-64763G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791573 | ||||||
| chr13:101791577
|
C | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-64767G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791577 | ||||||
| chr13:101791790
|
TA | T | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-64981delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791790 | ||||||
| chr13:101791920
|
C | A | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-65110G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101791920 | ||||||
| chr13:101792005
|
T | C | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.409-65195A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792005 | ||||||
| chr13:101792074
|
T | C | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-65264A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792074 | ||||||
| chr13:101792146
|
T | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-65336A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792146 | ||||||
| chr13:101792237
|
G | T | 207 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.409-65427C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792237 | ||||||
| chr13:101792246
|
A | G | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-65436T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792246 | ||||||
| chr13:101792271
|
T | C | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-65461A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792271 | ||||||
| chr13:101792584
|
C | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-65774G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792584 | ||||||
| chr13:101792608
|
T | C | 124 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.409-65798A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792608 | ||||||
| chr13:101792736
|
T | G | 1 | a0001c0001t0005g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.409-65926A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792736 | ||||||
| chr13:101792787
|
C | T | 1 | a0001c0001t0027g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.409-65977G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792787 | ||||||
| chr13:101792793
|
G | T | 15 | a0001c0001t0009g0159a0001c0001t0021g0170a0001c0001t0023g0157others(12): Show | 15 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-65983C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792793 | ||||||
| chr13:101792837
|
C | T | 1 | a0001c0001t0073g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.409-66027G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792837 | ||||||
| chr13:101792841
|
G | C | 246 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.409-66031C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792841 | ||||||
| chr13:101792872
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(3): Show | 6 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-66062G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792872 | ||||||
| chr13:101792877
|
T | C | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.409-66067A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792877 | ||||||
| chr13:101792899
|
T | TTA | 16 | a0001c0001t0016g0012a0001c0001t0021g0170a0001c0001t0023g0157others(13): Show | 16 | HG01255.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-66091_409-6609 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792899 | ||||||
| chr13:101792960
|
A | G | 1 | a0001c0001t0004g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.409-66150T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101792960 | ||||||
| chr13:101793029
|
A | T | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-66219T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793029 | ||||||
| chr13:101793177
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-66367A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793177 | ||||||
| chr13:101793182
|
C | A | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-66372G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793182 | ||||||
| chr13:101793193
|
T | C | 207 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.409-66383A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793193 | ||||||
| chr13:101793217
|
T | A | 15 | a0001c0001t0009g0159a0001c0001t0021g0170a0001c0001t0023g0157others(12): Show | 15 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-66407A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793217 | ||||||
| chr13:101793453
|
T | C | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-66643A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793453 | ||||||
| chr13:101793493
|
G | A | 133 | a0001c0001t0001g0075a0001c0001t0002g0055a0001c0001t0002g0065others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.409-66683C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793493 | ||||||
| chr13:101793513
|
C | T | 226 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-66703G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793513 | ||||||
| chr13:101793566
|
A | G | 10 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0019g0227others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-66756T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793566 | ||||||
| chr13:101793679
|
C | A | 254 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.409-66869G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793679 | ||||||
| chr13:101793785
|
T | C | 15 | a0001c0001t0009g0159a0001c0001t0021g0170a0001c0001t0023g0157others(12): Show | 15 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-66975A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793785 | ||||||
| chr13:101793954
|
A | G | 15 | a0001c0001t0009g0159a0001c0001t0021g0170a0001c0001t0023g0157others(12): Show | 15 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-67144T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793954 | ||||||
| chr13:101793999
|
C | T | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-67189G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101793999 | ||||||
| chr13:101794047
|
T | C | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-67237A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794047 | ||||||
| chr13:101794082
|
C | T | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-67272G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794082 | ||||||
| chr13:101794127
|
T | C | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.409-67317A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794127 | ||||||
| chr13:101794197
|
CT | C | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-67388delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794197 | ||||||
| chr13:101794211
|
T | C | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.409-67401A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794211 | ||||||
| chr13:101794231
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-67421G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794231 | ||||||
| chr13:101794247
|
GCT | G | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-67439_409-6743 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794247 | ||||||
| chr13:101794307
|
T | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-67497A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794307 | ||||||
| chr13:101794469
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-67659G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794469 | ||||||
| chr13:101794493
|
C | G | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-67683G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794493 | ||||||
| chr13:101794509
|
C | A | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-67699G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794509 | ||||||
| chr13:101794512
|
G | A | 2 | a0001c0001t0017g0135a0001c0001t0050g0001 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.409-67702C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794512 | ||||||
| chr13:101794538
|
C | A | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-67728G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794538 | ||||||
| chr13:101794539
|
TG | T | 5 | a0001c0001t0009g0159a0001c0001t0047g0165a0001c0001t0091g0117others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-67730delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794539 | ||||||
| chr13:101794552
|
G | A | 3 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.409-67742C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794552 | ||||||
| chr13:101794562
|
T | G | 94 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.409-67752A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794562 | ||||||
| chr13:101794609
|
T | C | 3 | a0001c0001t0017g0139a0001c0001t0146g0156a0001c0001t0148g0167 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.409-67799A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794609 | ||||||
| chr13:101794668
|
T | C | 21 | a0001c0001t0001g0075a0001c0001t0002g0101a0001c0001t0002g0109others(18): Show | 21 | HG00408.hp1 HG00621.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.409-67858A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794668 | ||||||
| chr13:101794692
|
A | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-67882T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794692 | ||||||
| chr13:101794745
|
T | C | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-67935A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794745 | ||||||
| chr13:101794879
|
T | C | 14 | a0001c0001t0021g0170a0001c0001t0023g0157a0001c0001t0023g0158others(11): Show | 14 | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.409-68069A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794879 | ||||||
| chr13:101794966
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-68156A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101794966 | ||||||
| chr13:101795007
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-68197A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795007 | ||||||
| chr13:101795087
|
T | G | 9 | a0001c0001t0017g0139a0001c0001t0047g0165a0001c0001t0051g0002others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-68277A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795087 | ||||||
| chr13:101795176
|
T | C | 224 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.409-68366A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795176 | ||||||
| chr13:101795275
|
CTGCCCT | C | 9 | a0001c0001t0017g0139a0001c0001t0047g0165a0001c0001t0051g0002others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.409-68471_409-6846 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795275 | ||||||
| chr13:101795285
|
C | T | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-68475G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795285 | ||||||
| chr13:101795422
|
G | C | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.409-68612C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795422 | ||||||
| chr13:101795488
|
T | C | 1 | a0001c0001t0134g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.409-68678A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795488 | ||||||
| chr13:101795538
|
T | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0093a0001c0001t0006g0097others(4): Show | 7 | HG00323.hp1 HG02015.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-68728A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795538 | ||||||
| chr13:101795589
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.409-68779T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795589 | ||||||
| chr13:101795668
|
G | A | 1 | a0001c0001t0008g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.409-68858C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795668 | ||||||
| chr13:101795744
|
A | G | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.409-68934T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101795744 | ||||||
| chr13:101796079
|
G | C | 1 | a0001c0001t0008g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.409-69269C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796079 | ||||||
| chr13:101796115
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-69305G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796115 | ||||||
| chr13:101796204
|
A | G | 2 | a0001c0001t0007g0042a0001c0001t0007g0043 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.409-69394T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796204 | ||||||
| chr13:101796329
|
C | G | 1 | a0001c0001t0046g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.409-69519G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796329 | ||||||
| chr13:101796346
|
T | C | 79 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.409-69536A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796346 | ||||||
| chr13:101796389
|
C | T | 258 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.409-69579G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796389 | ||||||
| chr13:101796472
|
T | A | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.409-69662A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796472 | ||||||
| chr13:101796519
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-69709G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796519 | ||||||
| chr13:101796807
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.409-69997G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796807 | ||||||
| chr13:101796811
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.409-70001G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796811 | ||||||
| chr13:101796823
|
C | G | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-70013G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796823 | ||||||
| chr13:101796878
|
A | T | 7 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0032g0039others(4): Show | 7 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-70068T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796878 | ||||||
| chr13:101796940
|
A | G | 225 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.409-70130T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796940 | ||||||
| chr13:101796961
|
C | T | 1 | a0001c0001t0033g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.409-70151G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796961 | ||||||
| chr13:101796973
|
A | G | 5 | a0001c0001t0017g0139a0001c0001t0051g0002a0001c0001t0146g0156others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-70163T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101796973 | ||||||
| chr13:101797118
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-70308G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797118 | ||||||
| chr13:101797138
|
AAC | A | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-70330_409-7032 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797138 | ||||||
| chr13:101797392
|
C | A | 2 | a0001c0001t0009g0241a0001c0001t0051g0002 | 2 | HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.409-70582G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797392 | ||||||
| chr13:101797416
|
T | G | 224 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.409-70606A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797416 | ||||||
| chr13:101797578
|
A | T | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-70768T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797578 | ||||||
| chr13:101797583
|
G | A | 2 | a0001c0001t0049g0218a0001c0001t0103g0134 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.409-70773C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797583 | ||||||
| chr13:101797734
|
G | GAT | 4 | a0001c0001t0075g0092a0001c0001t0089g0017a0001c0001t0118g0242others(1): Show | 4 | HG01192.hp1 HG01891.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797734 | ||||||
| chr13:101797735
|
A | ATATG | 65 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTG | 26 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0010g0153others(23): Show | 26 | HG00544.hp2 HG00621.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(1): Show |
31 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0004g0078others(28): Show | 31 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(3): Show |
22 | a0001c0001t0002g0055a0001c0001t0002g0098a0001c0001t0003g0030others(19): Show | 22 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(5): Show |
19 | a0001c0001t0002g0101a0001c0001t0002g0109a0001c0001t0003g0076others(16): Show | 19 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(7): Show |
22 | a0001c0001t0001g0075a0001c0001t0002g0104a0001c0001t0003g0058others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(9): Show |
7 | a0001c0001t0003g0031a0001c0001t0009g0203a0001c0001t0011g0150others(4): Show | 7 | HG00423.hp2 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-70926_409-7092 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATATGTGT others(11): Show |
1 | a0001c0001t0038g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.409-70926_409-7092 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
A | ATG | 7 | a0001c0001t0001g0132a0001c0001t0028g0018a0001c0001t0028g0019others(4): Show | 7 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-70927_409-7092 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
ATG | A | 12 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0019g0227others(9): Show | 12 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-70927_409-7092 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0002t0014g0116 | 3 | HG02257.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.409-70935_409-7092 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-70939_409-7092 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797735
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.409-70941_409-7092 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797735 | ||||||
| chr13:101797737
|
G | A | 25 | a0001c0001t0001g0016a0001c0001t0008g0152a0001c0001t0015g0124others(22): Show | 25 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.409-70927C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797737 | ||||||
| chr13:101797739
|
G | A | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.409-70929C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797739 | ||||||
| chr13:101797741
|
G | A | 1 | a0001c0001t0039g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.409-70931C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797741 | ||||||
| chr13:101797772
|
T | C | 207 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.408+70953A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGCGCGCG others(1): Show |
7 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(4): Show | 7 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+70952_408+7095 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGTGCGCG others(3): Show |
3 | a0001c0001t0046g0148a0001c0001t0046g0169a0001c0001t0079g0013 | 3 | HG02451.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+70952_408+7095 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGTGTGCG others(3): Show |
1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+70952_408+7095 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGTGTGCG others(3): Show |
1 | a0001c0001t0095g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.408+70952_408+7095 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.408+70952_408+7095 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797772
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+70952_408+7095 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797772 | ||||||
| chr13:101797774
|
T | C | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+70951A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797774 | ||||||
| chr13:101797847
|
C | A | 11 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0018g0221others(8): Show | 11 | HG01993.hp2 HG02074.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+70878G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797847 | ||||||
| chr13:101797879
|
A | C | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.408+70846T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797879 | ||||||
| chr13:101797988
|
G | T | 4 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0090g0015others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+70737C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101797988 | ||||||
| chr13:101798012
|
C | T | 3 | a0001c0001t0016g0012a0001c0001t0105g0133a0001c0001t0118g0242 | 3 | HG02280.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.408+70713G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798012 | ||||||
| chr13:101798019
|
C | T | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0113g0234others(2): Show | 5 | HG01255.hp2 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+70706G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798019 | ||||||
| chr13:101798107
|
T | A | 9 | a0001c0001t0017g0139a0001c0001t0047g0165a0001c0001t0051g0002others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.408+70618A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798107 | ||||||
| chr13:101798131
|
A | G | 3 | a0001c0001t0016g0012a0001c0001t0105g0133a0001c0001t0118g0242 | 3 | HG02280.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.408+70594T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798131 | ||||||
| chr13:101798133
|
A | C | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+70592T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798133 | ||||||
| chr13:101798154
|
C | T | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.408+70571G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798154 | ||||||
| chr13:101798194
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.408+70531G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798194 | ||||||
| chr13:101798217
|
C | T | 3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0011g0235 | 3 | HG01099.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.408+70508G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798217 | ||||||
| chr13:101798309
|
A | G | 2 | a0001c0001t0043g0253a0001c0001t0043g0254 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.408+70416T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798309 | ||||||
| chr13:101798312
|
G | C | 234 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.408+70413C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798312 | ||||||
| chr13:101798332
|
T | G | 222 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.408+70393A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798332 | ||||||
| chr13:101798339
|
T | G | 1 | a0001c0001t0144g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.408+70386A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798339 | ||||||
| chr13:101798382
|
C | T | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.408+70343G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798382 | ||||||
| chr13:101798592
|
T | C | 5 | a0001c0001t0017g0139a0001c0001t0051g0002a0001c0001t0146g0156others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+70133A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798592 | ||||||
| chr13:101798679
|
G | A | 131 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0002g0055others(128): Show | 131 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.408+70046C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798679 | ||||||
| chr13:101798769
|
C | T | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+69956G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798769 | ||||||
| chr13:101798792
|
G | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+69933C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798792 | ||||||
| chr13:101798881
|
C | T | 6 | a0001c0001t0004g0088a0001c0001t0009g0179a0001c0001t0009g0203others(3): Show | 6 | HG00423.hp2 HG00544.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+69844G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798881 | ||||||
| chr13:101798984
|
T | C | 1 | a0001c0001t0150g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.408+69741A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101798984 | ||||||
| chr13:101799168
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+69557G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799168 | ||||||
| chr13:101799226
|
T | C | 1 | a0001c0001t0027g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.408+69499A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799226 | ||||||
| chr13:101799382
|
A | T | 217 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.408+69343T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799382 | ||||||
| chr13:101799682
|
T | C | 235 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.408+69043A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799682 | ||||||
| chr13:101799683
|
G | A | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+69042C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799683 | ||||||
| chr13:101799841
|
G | C | 6 | a0001c0001t0005g0103a0001c0001t0012g0230a0001c0001t0021g0225others(3): Show | 6 | HG00597.hp2 HG01934.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+68884C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799841 | ||||||
| chr13:101799842
|
GACACCGA others(6): Show |
G | 6 | a0001c0001t0005g0103a0001c0001t0012g0230a0001c0001t0021g0225others(3): Show | 6 | HG00597.hp2 HG01934.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+68870_408+6888 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799842 | ||||||
| chr13:101799848
|
G | A | 1 | a0001c0001t0038g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.408+68877C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799848 | ||||||
| chr13:101799855
|
A | G | 1 | a0001c0001t0142g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.408+68870T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101799855 | ||||||
| chr13:101800076
|
T | C | 11 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0018g0221others(8): Show | 11 | HG01993.hp2 HG02074.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+68649A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800076 | ||||||
| chr13:101800411
|
T | A | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+68314A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800411 | ||||||
| chr13:101800497
|
G | A | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+68228C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800497 | ||||||
| chr13:101800629
|
C | A | 3 | a0001c0001t0025g0008a0001c0001t0043g0253a0001c0001t0043g0254 | 3 | NA18970.hp2 NA19000.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.408+68096G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800629 | ||||||
| chr13:101800663
|
A | T | 11 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0018g0221others(8): Show | 11 | HG01993.hp2 HG02074.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+68062T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800663 | ||||||
| chr13:101800727
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.408+67998G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800727 | ||||||
| chr13:101800790
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+67935T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800790 | ||||||
| chr13:101800918
|
C | G | 77 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.408+67807G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101800918 | ||||||
| chr13:101801064
|
C | T | 7 | a0001c0001t0047g0165a0001c0001t0061g0025a0001c0001t0091g0117others(4): Show | 7 | HG02257.hp1 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+67661G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801064 | ||||||
| chr13:101801212
|
T | A | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+67513A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801212 | ||||||
| chr13:101801274
|
C | T | 1 | a0001c0001t0033g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.408+67451G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801274 | ||||||
| chr13:101801352
|
AT | A | 19 | a0001c0001t0009g0159a0001c0001t0023g0157a0001c0001t0023g0158others(16): Show | 19 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.408+67372delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801352 | ||||||
| chr13:101801357
|
T | A | 207 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.408+67368A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801357 | ||||||
| chr13:101801773
|
G | T | 197 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.408+66952C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801773 | ||||||
| chr13:101801782
|
G | A | 1 | a0001c0001t0021g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.408+66943C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801782 | ||||||
| chr13:101801918
|
C | T | 1 | a0001c0001t0138g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.408+66807G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101801918 | ||||||
| chr13:101802117
|
G | A | 197 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(194): Show | 197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.408+66608C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802117 | ||||||
| chr13:101802154
|
A | T | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.408+66571T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802154 | ||||||
| chr13:101802168
|
C | T | 12 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(9): Show | 12 | HG01081.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.408+66557G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802168 | ||||||
| chr13:101802308
|
T | G | 264 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.408+66417A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802308 | ||||||
| chr13:101802397
|
G | C | 3 | a0001c0001t0040g0188a0001c0001t0040g0189a0001c0001t0109g0199 | 3 | NA18948.hp1 NA18964.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.408+66328C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802397 | ||||||
| chr13:101802442
|
G | A | 185 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.408+66283C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802442 | ||||||
| chr13:101802533
|
C | T | 264 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.408+66192G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802533 | ||||||
| chr13:101802733
|
G | T | 2 | a0001c0001t0131g0162a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.408+65992C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802733 | ||||||
| chr13:101802736
|
G | A | 2 | a0001c0001t0084g0040a0001c0001t0135g0183 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.408+65989C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802736 | ||||||
| chr13:101802839
|
G | A | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+65886C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802839 | ||||||
| chr13:101802840
|
T | C | 1 | a0001c0001t0086g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.408+65885A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802840 | ||||||
| chr13:101802956
|
A | C | 32 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0006g0085others(29): Show | 32 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.408+65769T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101802956 | ||||||
| chr13:101803128
|
C | CT | 11 | a0001c0001t0015g0114a0001c0001t0034g0054a0001c0001t0035g0044others(8): Show | 11 | HG00099.hp2 HG00597.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+65596dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803128 | ||||||
| chr13:101803128
|
CT | C | 43 | a0001c0001t0001g0127a0001c0001t0005g0103a0001c0001t0006g0083others(40): Show | 43 | HG01081.hp2 HG01109.hp2 HG01516.hp1 others(40): Show |
intron_variant | MODIFIER | c.408+65596delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803128 | ||||||
| chr13:101803257
|
C | A | 76 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(73): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.408+65468G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803257 | ||||||
| chr13:101803306
|
A | T | 137 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0002g0055others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.408+65419T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803306 | ||||||
| chr13:101803461
|
G | A | 32 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0006g0085others(29): Show | 32 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.408+65264C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803461 | ||||||
| chr13:101803546
|
TTTGTATG others(29): Show |
T | 169 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0132others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.408+65143_408+6517 others(40): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803546 | ||||||
| chr13:101803916
|
G | A | 1 | a0001c0001t0047g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.408+64809C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101803916 | ||||||
| chr13:101804089
|
T | G | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.408+64636A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804089 | ||||||
| chr13:101804599
|
C | G | 1 | a0001c0001t0106g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.408+64126G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804599 | ||||||
| chr13:101804673
|
C | CAT | 17 | a0001c0001t0003g0110a0001c0001t0008g0152a0001c0001t0010g0153others(14): Show | 17 | HG00323.hp2 HG00423.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.408+64050_408+6405 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804673 | ||||||
| chr13:101804687
|
T | C | 1 | a0001c0001t0083g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.408+64038A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804687 | ||||||
| chr13:101804735
|
T | A | 6 | a0001c0001t0001g0016a0001c0001t0017g0139a0001c0001t0021g0170others(3): Show | 6 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+63990A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804735 | ||||||
| chr13:101804793
|
C | G | 9 | a0001c0001t0003g0110a0001c0001t0008g0152a0001c0001t0032g0039others(6): Show | 9 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+63932G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804793 | ||||||
| chr13:101804816
|
T | C | 5 | a0001c0001t0009g0159a0001c0001t0028g0018a0001c0001t0028g0019others(2): Show | 5 | HG03139.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+63909A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804816 | ||||||
| chr13:101804818
|
G | C | 1 | a0001c0001t0085g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.408+63907C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804818 | ||||||
| chr13:101804833
|
A | T | 39 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.408+63892T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804833 | ||||||
| chr13:101804909
|
T | C | 31 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0006g0085others(28): Show | 31 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.408+63816A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804909 | ||||||
| chr13:101804948
|
C | T | 2 | a0001c0001t0021g0170a0001c0001t0051g0002 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.408+63777G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101804948 | ||||||
| chr13:101805047
|
T | C | 2 | a0001c0001t0131g0162a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.408+63678A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805047 | ||||||
| chr13:101805146
|
A | G | 76 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(73): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.408+63579T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805146 | ||||||
| chr13:101805205
|
G | A | 1 | a0001c0001t0142g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.408+63520C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805205 | ||||||
| chr13:101805320
|
A | G | 33 | a0001c0001t0001g0132a0001c0001t0005g0067a0001c0001t0006g0083others(30): Show | 33 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.408+63405T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805320 | ||||||
| chr13:101805633
|
A | C | 76 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(73): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.408+63092T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805633 | ||||||
| chr13:101805671
|
G | A | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+63054C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805671 | ||||||
| chr13:101805750
|
A | C | 1 | a0001c0001t0130g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.408+62975T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805750 | ||||||
| chr13:101805809
|
C | A | 183 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0132others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.408+62916G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805809 | ||||||
| chr13:101805858
|
C | G | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+62867G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805858 | ||||||
| chr13:101805965
|
G | C | 10 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0015g0114others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+62760C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805965 | ||||||
| chr13:101805983
|
T | C | 1 | a0001c0001t0089g0017 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.408+62742A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101805983 | ||||||
| chr13:101806197
|
G | T | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+62528C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806197 | ||||||
| chr13:101806235
|
C | T | 1 | a0001c0001t0098g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.408+62490G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806235 | ||||||
| chr13:101806413
|
C | T | 1 | a0001c0001t0012g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.408+62312G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806413 | ||||||
| chr13:101806423
|
G | GAAA | 8 | a0001c0001t0008g0233a0001c0001t0009g0241a0001c0001t0045g0214others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+62299_408+6230 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806423 | ||||||
| chr13:101806423
|
GA | G | 30 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(27): Show | 30 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+62301delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806423 | ||||||
| chr13:101806452
|
T | C | 30 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(27): Show | 30 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+62273A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806452 | ||||||
| chr13:101806463
|
A | T | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+62262T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806463 | ||||||
| chr13:101806474
|
A | T | 30 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(27): Show | 30 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+62251T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806474 | ||||||
| chr13:101806475
|
T | A | 215 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.408+62250A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806475 | ||||||
| chr13:101806551
|
G | A | 1 | a0001c0001t0081g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+62174C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806551 | ||||||
| chr13:101806714
|
T | G | 4 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0154g0145others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+62011A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806714 | ||||||
| chr13:101806917
|
T | G | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+61808A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806917 | ||||||
| chr13:101806953
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0017g0139a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+61772G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101806953 | ||||||
| chr13:101807036
|
C | A | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+61689G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807036 | ||||||
| chr13:101807062
|
G | A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+61663C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807062 | ||||||
| chr13:101807199
|
T | C | 208 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.408+61526A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807199 | ||||||
| chr13:101807214
|
T | C | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.408+61511A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807214 | ||||||
| chr13:101807235
|
A | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+61490T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807235 | ||||||
| chr13:101807251
|
T | C | 208 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.408+61474A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807251 | ||||||
| chr13:101807383
|
T | C | 208 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.408+61342A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807383 | ||||||
| chr13:101807509
|
G | C | 208 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.408+61216C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807509 | ||||||
| chr13:101807576
|
A | G | 208 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.408+61149T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807576 | ||||||
| chr13:101807675
|
T | A | 1 | a0001c0001t0025g0007 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.408+61050A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807675 | ||||||
| chr13:101807708
|
T | C | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+61017A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807708 | ||||||
| chr13:101807714
|
C | T | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+61011G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807714 | ||||||
| chr13:101807715
|
G | A | 5 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0018g0221others(2): Show | 5 | HG01993.hp2 HG02074.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+61010C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807715 | ||||||
| chr13:101807810
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0084g0040a0001c0001t0135g0183 | 3 | HG01257.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.408+60915A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807810 | ||||||
| chr13:101807872
|
A | C | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+60853T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807872 | ||||||
| chr13:101807962
|
A | G | 2 | a0001c0001t0131g0162a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.408+60763T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807962 | ||||||
| chr13:101807991
|
G | A | 206 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.408+60734C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101807991 | ||||||
| chr13:101808055
|
T | C | 1 | a0001c0001t0114g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.408+60670A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808055 | ||||||
| chr13:101808098
|
T | C | 206 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.408+60627A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808098 | ||||||
| chr13:101808141
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+60584A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808141 | ||||||
| chr13:101808414
|
T | C | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+60311A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808414 | ||||||
| chr13:101808679
|
A | G | 170 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(167): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.408+60046T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808679 | ||||||
| chr13:101808717
|
T | C | 2 | a0001c0001t0073g0045a0001c0001t0139g0181 | 2 | HG01934.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.408+60008A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808717 | ||||||
| chr13:101808741
|
A | AT | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+59983dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808741 | ||||||
| chr13:101808788
|
A | G | 206 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.408+59937T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808788 | ||||||
| chr13:101808815
|
G | T | 32 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0006g0085others(29): Show | 32 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.408+59910C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808815 | ||||||
| chr13:101808839
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.408+59886A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808839 | ||||||
| chr13:101808901
|
A | C | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+59824T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808901 | ||||||
| chr13:101808934
|
G | A | 9 | a0001c0001t0003g0110a0001c0001t0008g0152a0001c0001t0032g0039others(6): Show | 9 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+59791C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808934 | ||||||
| chr13:101808956
|
G | A | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+59769C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101808956 | ||||||
| chr13:101809036
|
T | C | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0022g0196 | 3 | NA18962.hp1 NA18992.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.408+59689A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809036 | ||||||
| chr13:101809161
|
C | CCT | 189 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(186): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.408+59563_408+5956 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809161 | ||||||
| chr13:101809181
|
C | A | 260 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.408+59544G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809181 | ||||||
| chr13:101809567
|
A | C | 1 | a0001c0001t0038g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.408+59158T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809567 | ||||||
| chr13:101809626
|
G | T | 1 | a0001c0001t0042g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.408+59099C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809626 | ||||||
| chr13:101809643
|
C | G | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0102g0138others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+59082G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809643 | ||||||
| chr13:101809797
|
A | C | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0102g0138others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+58928T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809797 | ||||||
| chr13:101809949
|
A | C | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+58776T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101809949 | ||||||
| chr13:101810056
|
A | G | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+58669T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810056 | ||||||
| chr13:101810078
|
T | A | 1 | a0001c0001t0046g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.408+58647A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810078 | ||||||
| chr13:101810179
|
A | G | 1 | a0001c0001t0039g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.408+58546T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810179 | ||||||
| chr13:101810260
|
T | C | 7 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0139others(4): Show | 7 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+58465A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810260 | ||||||
| chr13:101810321
|
G | C | 205 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.408+58404C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810321 | ||||||
| chr13:101810441
|
T | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408+58284A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810441 | ||||||
| chr13:101810454
|
T | C | 1 | a0001c0001t0066g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.408+58271A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810454 | ||||||
| chr13:101810506
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+58219G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810506 | ||||||
| chr13:101810507
|
A | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+58218T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810507 | ||||||
| chr13:101810530
|
T | G | 205 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.408+58195A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810530 | ||||||
| chr13:101810539
|
T | C | 173 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(170): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.408+58186A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810539 | ||||||
| chr13:101810730
|
C | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+57995G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810730 | ||||||
| chr13:101810827
|
G | A | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+57898C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810827 | ||||||
| chr13:101810844
|
G | A | 30 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(27): Show | 30 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.408+57881C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810844 | ||||||
| chr13:101810880
|
G | T | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+57845C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810880 | ||||||
| chr13:101810924
|
T | C | 173 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(170): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.408+57801A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810924 | ||||||
| chr13:101810926
|
T | A | 1 | a0001c0001t0108g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.408+57799A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810926 | ||||||
| chr13:101810975
|
C | T | 30 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(27): Show | 30 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.408+57750G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101810975 | ||||||
| chr13:101811031
|
C | T | 3 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0090g0015 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.408+57694G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811031 | ||||||
| chr13:101811032
|
GC | G | 9 | a0001c0001t0003g0110a0001c0001t0008g0152a0001c0001t0032g0039others(6): Show | 9 | HG00323.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+57692delG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811032 | ||||||
| chr13:101811033
|
C | CCCCCCG | 27 | a0001c0001t0001g0029a0001c0001t0002g0104a0001c0001t0004g0082others(24): Show | 27 | HG00597.hp2 HG01099.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.408+57691_408+5769 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811033 | ||||||
| chr13:101811034
|
C | CCCCCG | 147 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0036others(144): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.408+57690_408+5769 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811034 | ||||||
| chr13:101811038
|
C | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+57687G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811038 | ||||||
| chr13:101811041
|
G | C | 174 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(171): Show | 174 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.408+57684C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811041 | ||||||
| chr13:101811048
|
G | A | 174 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(171): Show | 174 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.408+57677C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811048 | ||||||
| chr13:101811115
|
T | C | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.408+57610A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811115 | ||||||
| chr13:101811324
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0011g0223 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.408+57401A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811324 | ||||||
| chr13:101811504
|
T | C | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.408+57221A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811504 | ||||||
| chr13:101811526
|
G | A | 1 | a0001c0001t0108g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.408+57199C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811526 | ||||||
| chr13:101811694
|
T | C | 264 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.408+57031A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811694 | ||||||
| chr13:101811838
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.408+56887C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811838 | ||||||
| chr13:101811861
|
C | G | 1 | a0001c0001t0005g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.408+56864G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811861 | ||||||
| chr13:101811996
|
T | C | 30 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(27): Show | 30 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.408+56729A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101811996 | ||||||
| chr13:101812060
|
G | A | 204 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.408+56665C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812060 | ||||||
| chr13:101812060
|
G | T | 30 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(27): Show | 30 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+56665C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812060 | ||||||
| chr13:101812069
|
G | A | 30 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(27): Show | 30 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.408+56656C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812069 | ||||||
| chr13:101812112
|
A | G | 6 | a0001c0001t0019g0244a0001c0001t0028g0018a0001c0001t0028g0019others(3): Show | 6 | HG02630.hp1 HG02976.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+56613T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812112 | ||||||
| chr13:101812371
|
T | C | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+56354A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812371 | ||||||
| chr13:101812611
|
CTA | C | 4 | a0001c0001t0031g0035a0001c0001t0045g0214a0001c0001t0084g0040others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+56112_408+5611 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATA | C | 15 | a0001c0001t0001g0036a0001c0001t0011g0150a0001c0001t0013g0142others(12): Show | 15 | HG00280.hp2 HG01168.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.408+56110_408+5611 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATA | C | 20 | a0001c0001t0003g0058a0001c0001t0007g0037a0001c0001t0007g0042others(17): Show | 20 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.408+56108_408+5611 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(1): Show |
C | 16 | a0001c0001t0003g0030a0001c0001t0003g0076a0001c0001t0006g0059others(13): Show | 16 | HG00544.hp1 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.408+56106_408+5611 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(3): Show |
C | 13 | a0001c0001t0001g0033a0001c0001t0001g0075a0001c0001t0001g0093others(10): Show | 13 | HG00408.hp1 HG02523.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.408+56104_408+5611 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(5): Show |
C | 5 | a0001c0001t0004g0057a0001c0001t0010g0248a0001c0001t0030g0032others(2): Show | 5 | HG02074.hp1 HG02300.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+56102_408+5611 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(7): Show |
C | 8 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0020g0250others(5): Show | 8 | HG00544.hp2 HG01192.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+56100_408+5611 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(9): Show |
C | 3 | a0001c0001t0009g0241a0001c0001t0039g0185a0001c0001t0101g0105 | 3 | HG02970.hp2 NA18977.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.408+56098_408+5611 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(11): Show |
C | 3 | a0001c0001t0002g0096a0001c0001t0036g0062a0001c0001t0140g0192 | 3 | HG02698.hp1 HG03490.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.408+56096_408+5611 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(13): Show |
C | 4 | a0001c0001t0015g0114a0001c0001t0018g0221a0001c0001t0019g0244others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+56094_408+5611 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812611
|
CTATATAT others(17): Show |
C | 4 | a0001c0001t0002g0104a0001c0001t0021g0225a0001c0001t0139g0181others(1): Show | 4 | HG01934.hp2 HG02015.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+56090_408+5611 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812611 | ||||||
| chr13:101812626
|
TATATATA others(18): Show |
T | 1 | a0001c0001t0073g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.408+56074_408+5609 others(29): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812626 | ||||||
| chr13:101812631
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0005g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.408+56070_408+5609 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812631 | ||||||
| chr13:101812632
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0030g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.408+56072_408+5609 others(25): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812632 | ||||||
| chr13:101812633
|
ATATATAT others(15): Show |
A | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+56070_408+5609 others(26): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812633 | ||||||
| chr13:101812633
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.408+56068_408+5609 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812633 | ||||||
| chr13:101812633
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0089g0017 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.408+56063_408+5609 others(33): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812633 | ||||||
| chr13:101812634
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0011g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.408+56072_408+5609 others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812634 | ||||||
| chr13:101812635
|
ATATATAT others(12): Show |
A | 12 | a0001c0001t0002g0055a0001c0001t0002g0098a0001c0001t0004g0070others(9): Show | 12 | HG00438.hp2 HG00597.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+56071_408+5608 others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812635 | ||||||
| chr13:101812635
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0004g0088a0001c0001t0012g0237 | 2 | HG03491.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.408+56070_408+5608 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812635 | ||||||
| chr13:101812635
|
ATATATAT others(20): Show |
A | 2 | a0001c0001t0023g0157a0001c0001t0023g0158 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.408+56063_408+5608 others(31): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812635 | ||||||
| chr13:101812636
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0036g0061 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.408+56072_408+5608 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812636 | ||||||
| chr13:101812637
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0039g0177a0001c0001t0064g0126 | 2 | HG03688.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.408+56071_408+5608 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812637 | ||||||
| chr13:101812637
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0041g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.408+56070_408+5608 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812637 | ||||||
| chr13:101812637
|
ATATATAT others(12): Show |
A | 8 | a0001c0001t0008g0152a0001c0001t0020g0187a0001c0001t0032g0039others(5): Show | 8 | HG00323.hp2 HG00438.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+56069_408+5608 others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812637 | ||||||
| chr13:101812637
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+56065_408+5608 others(27): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812637 | ||||||
| chr13:101812638
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0022g0195a0001c0001t0131g0162 | 2 | HG03225.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.408+56076_408+5608 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812638 | ||||||
| chr13:101812638
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0055g0006 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.408+56074_408+5608 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812638 | ||||||
| chr13:101812638
|
TATATATA others(8): Show |
T | 3 | a0001c0001t0029g0099a0001c0001t0033g0049a0001c0001t0117g0229 | 3 | HG00408.hp2 HG02074.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.408+56072_408+5608 others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812638 | ||||||
| chr13:101812639
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0006g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.408+56071_408+5608 others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812639 | ||||||
| chr13:101812639
|
ATATATAT others(9): Show |
A | 3 | a0001c0001t0003g0110a0001c0001t0010g0153a0001c0001t0027g0026 | 3 | HG01081.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.408+56070_408+5608 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812639 | ||||||
| chr13:101812639
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0108g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.408+56069_408+5608 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812639 | ||||||
| chr13:101812639
|
ATATATAT others(12): Show |
A | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0102g0138others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+56067_408+5608 others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812639 | ||||||
| chr13:101812639
|
ATATATAT others(13): Show |
A | 4 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+56066_408+5608 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812639 | ||||||
| chr13:101812640
|
TATATATA | T | 4 | a0001c0001t0001g0132a0001c0001t0109g0199a0001c0001t0121g0160others(1): Show | 4 | HG01099.hp1 HG02258.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+56078_408+5608 others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812640 | ||||||
| chr13:101812640
|
TATATATA others(4): Show |
T | 4 | a0001c0001t0006g0097a0001c0001t0022g0194a0001c0001t0022g0196others(1): Show | 4 | HG00323.hp1 HG03195.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+56074_408+5608 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812640 | ||||||
| chr13:101812640
|
TATATATA others(6): Show |
T | 5 | a0001c0001t0003g0106a0001c0001t0010g0249a0001c0001t0033g0095others(2): Show | 5 | HG00423.hp1 HG01993.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+56072_408+5608 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812640 | ||||||
| chr13:101812641
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0065a0001c0001t0026g0027 | 2 | HG00621.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.408+56071_408+5608 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812641 | ||||||
| chr13:101812641
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0018g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.408+56070_408+5608 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812641 | ||||||
| chr13:101812641
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+56069_408+5608 others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812641 | ||||||
| chr13:101812641
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+56068_408+5608 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812641 | ||||||
| chr13:101812641
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0090g0015a0001c0001t0160g0258 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.408+56063_408+5608 others(25): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812641 | ||||||
| chr13:101812642
|
TATATATA | T | 3 | a0001c0001t0015g0124a0001c0001t0021g0210a0001c0001t0038g0125 | 3 | HG02738.hp1 HG03490.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.408+56076_408+5608 others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812642 | ||||||
| chr13:101812642
|
TATATATA others(2): Show |
T | 6 | a0001c0001t0003g0031a0001c0001t0008g0208a0001c0001t0025g0008others(3): Show | 6 | NA18962.hp2 NA18970.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+56074_408+5608 others(13): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812642 | ||||||
| chr13:101812642
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0005g0102a0001c0001t0112g0171 | 2 | HG00621.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.408+56072_408+5608 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812642 | ||||||
| chr13:101812643
|
A | T | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+56082T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812643 | ||||||
| chr13:101812643
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0054g0004 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408+56071_408+5608 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812643 | ||||||
| chr13:101812643
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+56070_408+5608 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812643 | ||||||
| chr13:101812643
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0020g0217a0001c0001t0042g0231 | 2 | NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.408+56068_408+5608 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812643 | ||||||
| chr13:101812643
|
ATATATAT others(9): Show |
A | 2 | a0001c0001t0046g0169a0001c0001t0074g0122 | 2 | HG03704.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+56066_408+5608 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812643 | ||||||
| chr13:101812644
|
TATATATA | T | 8 | a0001c0001t0007g0043a0001c0001t0013g0212a0001c0001t0017g0136others(5): Show | 8 | HG01169.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+56074_408+5608 others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812644 | ||||||
| chr13:101812645
|
A | T | 2 | a0001c0001t0092g0113a0001c0001t0147g0220 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.408+56080T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812645
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0103g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408+56070_408+5607 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812645
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0146g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.408+56069_408+5607 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812645
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0044g0178a0001c0001t0156g0256 | 2 | NA19043.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.408+56068_408+5607 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812645
|
ATATATAT others(6): Show |
A | 1 | a0001c0002t0127g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.408+56067_408+5607 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812645
|
ATATATAT others(7): Show |
A | 1 | a0001c0002t0128g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.408+56066_408+5607 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812645 | ||||||
| chr13:101812646
|
TATATA | T | 4 | a0001c0001t0001g0127a0001c0001t0011g0223a0001c0001t0013g0143others(1): Show | 4 | HG01109.hp2 HG02738.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+56074_408+5607 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812646 | ||||||
| chr13:101812646
|
TATATATA | T | 4 | a0001c0001t0013g0144a0001c0001t0049g0141a0001c0001t0095g0022others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+56072_408+5607 others(11): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812646 | ||||||
| chr13:101812647
|
A | T | 14 | a0001c0001t0009g0203a0001c0001t0031g0035a0001c0001t0037g0066others(11): Show | 14 | HG00423.hp2 HG00642.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+56078T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812647 | ||||||
| chr13:101812647
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0049g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.408+56068_408+5607 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812647 | ||||||
| chr13:101812647
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0016a0001c0001t0017g0139 | 2 | HG01993.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.408+56067_408+5607 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812647 | ||||||
| chr13:101812648
|
TATATA | T | 3 | a0001c0001t0016g0130a0001c0001t0047g0213a0001c0001t0130g0219 | 3 | HG01891.hp2 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.408+56072_408+5607 others(9): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812648 | ||||||
| chr13:101812649
|
A | ATT | 3 | a0001c0001t0001g0051a0001c0001t0011g0235a0001c0001t0133g0211 | 3 | HG01175.hp2 HG01952.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.408+56075_408+5607 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812649 | ||||||
| chr13:101812649
|
A | T | 37 | a0001c0001t0001g0132a0001c0001t0008g0233a0001c0001t0009g0179others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.408+56076T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812649 | ||||||
| chr13:101812651
|
A | T | 71 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.408+56074T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812651 | ||||||
| chr13:101812653
|
A | ATATATTT others(6): Show |
1 | a0001c0001t0026g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.408+56071_408+5607 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812653 | ||||||
| chr13:101812653
|
A | ATATTTTT others(5): Show |
1 | a0001c0001t0056g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.408+56071_408+5607 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812653 | ||||||
| chr13:101812653
|
A | T | 134 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.408+56072T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812653 | ||||||
| chr13:101812682
|
T | A | 42 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(39): Show | 42 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.408+56043A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812682 | ||||||
| chr13:101812735
|
C | T | 152 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.408+55990G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812735 | ||||||
| chr13:101812797
|
G | A | 31 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(28): Show | 31 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.408+55928C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101812797 | ||||||
| chr13:101813177
|
C | G | 2 | a0001c0001t0019g0244a0001c0001t0162g0265 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.408+55548G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813177 | ||||||
| chr13:101813301
|
G | A | 207 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.408+55424C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813301 | ||||||
| chr13:101813502
|
CA | C | 18 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+55222delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813502 | ||||||
| chr13:101813510
|
A | G | 1 | a0001c0001t0085g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.408+55215T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813510 | ||||||
| chr13:101813523
|
T | G | 3 | a0001c0001t0032g0039a0001c0001t0032g0060a0001c0001t0132g0184 | 3 | HG01256.hp2 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.408+55202A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813523 | ||||||
| chr13:101813612
|
C | G | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+55113G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813612 | ||||||
| chr13:101813665
|
T | C | 2 | a0001c0001t0015g0124a0001c0001t0110g0182 | 2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.408+55060A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813665 | ||||||
| chr13:101813676
|
GA | G | 41 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0006g0073others(38): Show | 41 | HG00423.hp1 HG01081.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.408+55048delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813676 | ||||||
| chr13:101813985
|
G | T | 24 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0013g0142others(21): Show | 24 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.408+54740C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101813985 | ||||||
| chr13:101814250
|
G | A | 1 | a0001c0001t0114g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.408+54475C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814250 | ||||||
| chr13:101814495
|
A | G | 1 | a0001c0001t0123g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.408+54230T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814495 | ||||||
| chr13:101814768
|
T | C | 1 | a0001c0001t0052g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.408+53957A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814768 | ||||||
| chr13:101814772
|
A | T | 2 | a0001c0001t0028g0018a0001c0001t0028g0019 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.408+53953T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814772 | ||||||
| chr13:101814907
|
G | A | 130 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0002g0055others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.408+53818C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814907 | ||||||
| chr13:101814911
|
G | A | 2 | a0001c0001t0019g0244a0001c0001t0162g0265 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.408+53814C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814911 | ||||||
| chr13:101814973
|
G | A | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+53752C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814973 | ||||||
| chr13:101814990
|
CT | C | 75 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.408+53734delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814990 | ||||||
| chr13:101814991
|
T | C | 1 | a0001c0001t0037g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.408+53734A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101814991 | ||||||
| chr13:101815043
|
G | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+53682C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815043 | ||||||
| chr13:101815086
|
T | C | 2 | a0001c0001t0089g0017a0001c0001t0093g0111 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.408+53639A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815086 | ||||||
| chr13:101815122
|
G | A | 10 | a0001c0001t0015g0124a0001c0001t0023g0157a0001c0001t0023g0158others(7): Show | 10 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+53603C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815122 | ||||||
| chr13:101815178
|
G | C | 130 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0002g0055others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.408+53547C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815178 | ||||||
| chr13:101815305
|
T | C | 207 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.408+53420A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815305 | ||||||
| chr13:101815650
|
AGGG | A | 17 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.408+53072_408+5307 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815650 | ||||||
| chr13:101815654
|
A | T | 17 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.408+53071T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815654 | ||||||
| chr13:101815729
|
C | T | 103 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.408+52996G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815729 | ||||||
| chr13:101815822
|
G | A | 90 | a0001c0001t0001g0132a0001c0001t0003g0106a0001c0001t0003g0110others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.408+52903C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815822 | ||||||
| chr13:101815906
|
A | T | 134 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(131): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.408+52819T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815906 | ||||||
| chr13:101815927
|
A | G | 3 | a0001c0001t0019g0244a0001c0001t0066g0112a0001c0001t0162g0265 | 3 | HG02630.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.408+52798T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815927 | ||||||
| chr13:101815995
|
G | C | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+52730C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101815995 | ||||||
| chr13:101816015
|
T | TA | 140 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.408+52709dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816015 | ||||||
| chr13:101816037
|
G | A | 2 | a0001c0001t0089g0017a0001c0001t0093g0111 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.408+52688C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816037 | ||||||
| chr13:101816162
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.408+52563A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816162 | ||||||
| chr13:101816176
|
A | G | 4 | a0001c0001t0009g0159a0001c0001t0118g0242a0001c0001t0131g0162others(1): Show | 4 | HG02818.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+52549T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816176 | ||||||
| chr13:101816178
|
C | G | 135 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.408+52547G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816178 | ||||||
| chr13:101816269
|
C | CA | 6 | a0001c0001t0008g0208a0001c0001t0022g0194a0001c0001t0039g0177others(3): Show | 6 | HG01175.hp1 HG02280.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+52455dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAA | 7 | a0001c0001t0003g0110a0001c0001t0008g0152a0001c0001t0032g0039others(4): Show | 7 | HG00323.hp2 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+52450_408+5245 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0023g0157a0001c0001t0047g0165a0001c0001t0091g0117others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+52447_408+5245 others(13): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(3): Show |
26 | a0001c0001t0001g0132a0001c0001t0011g0235a0001c0001t0023g0158others(23): Show | 26 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.408+52446_408+5245 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0006g0083a0001c0001t0046g0148a0001c0001t0056g0107others(4): Show | 7 | HG01081.hp2 HG01516.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+52445_408+5245 others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0017g0135a0001c0001t0050g0001a0001c0001t0066g0112others(2): Show | 5 | HG02451.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+52444_408+5245 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0103g0134a0001c0001t0150g0146a0001c0001t0157g0262 | 3 | HG02145.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.408+52443_408+5245 others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+52442_408+5245 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0019g0244a0001c0001t0162g0265 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.408+52441_408+5245 others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0010g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.408+52455_408+5245 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0124g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.408+52455_408+5245 others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0010g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.408+52455_408+5245 others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0009g0241a0001c0001t0026g0027a0001c0001t0061g0025 | 3 | HG01256.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.408+52455_408+5245 others(27): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0016g0012a0001c0002t0127g0224 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.408+52455_408+5245 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(18): Show |
7 | a0001c0001t0018g0236a0001c0001t0021g0170a0001c0001t0030g0032others(4): Show | 7 | HG02559.hp1 HG02970.hp1 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+52455_408+5245 others(29): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(19): Show |
7 | a0001c0001t0008g0173a0001c0001t0010g0153a0001c0001t0012g0191others(4): Show | 7 | HG01081.hp1 HG01192.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+52455_408+5245 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+52455_408+5245 others(31): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0006g0073a0001c0001t0044g0178 | 2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.408+52455_408+5245 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(22): Show |
3 | a0001c0001t0003g0106a0001c0001t0004g0057a0001c0001t0114g0186 | 3 | HG01993.hp2 HG02135.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.408+52455_408+5245 others(33): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(24): Show |
3 | a0001c0001t0025g0007a0001c0001t0053g0005a0001c0001t0055g0006 | 3 | NA18978.hp2 NA18993.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.408+52455_408+5245 others(35): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0042g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.408+52455_408+5245 others(36): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816269
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+52455_408+5245 others(38): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816269 | ||||||
| chr13:101816286
|
T | G | 90 | a0001c0001t0001g0132a0001c0001t0003g0106a0001c0001t0003g0110others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.408+52439A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816286 | ||||||
| chr13:101816298
|
G | A | 90 | a0001c0001t0001g0132a0001c0001t0003g0106a0001c0001t0003g0110others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.408+52427C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816298 | ||||||
| chr13:101816304
|
T | C | 32 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0009g0159others(29): Show | 32 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.408+52421A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816304 | ||||||
| chr13:101816411
|
A | G | 2 | a0001c0001t0006g0059a0001c0001t0011g0223 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.408+52314T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816411 | ||||||
| chr13:101816545
|
G | T | 3 | a0001c0001t0009g0159a0001c0001t0131g0162a0001c0001t0157g0262 | 3 | HG02818.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.408+52180C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816545 | ||||||
| chr13:101816675
|
A | G | 2 | a0001c0001t0150g0146a0001c0001t0158g0264 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.408+52050T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816675 | ||||||
| chr13:101816713
|
T | C | 2 | a0001c0001t0089g0017a0001c0001t0093g0111 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.408+52012A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816713 | ||||||
| chr13:101816768
|
A | G | 265 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.408+51957T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816768 | ||||||
| chr13:101816858
|
T | C | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+51867A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101816858 | ||||||
| chr13:101817105
|
T | A | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.408+51620A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817105 | ||||||
| chr13:101817171
|
A | G | 135 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.408+51554T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817171 | ||||||
| chr13:101817197
|
G | C | 2 | a0001c0001t0137g0240a0001c0001t0143g0239 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.408+51528C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817197 | ||||||
| chr13:101817199
|
A | G | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.408+51526T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817199 | ||||||
| chr13:101817221
|
A | G | 46 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.408+51504T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817221 | ||||||
| chr13:101817256
|
T | G | 2 | a0001c0001t0019g0244a0001c0001t0162g0265 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.408+51469A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817256 | ||||||
| chr13:101817314
|
C | T | 2 | a0001c0001t0089g0017a0001c0001t0093g0111 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.408+51411G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817314 | ||||||
| chr13:101817437
|
A | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+51288T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817437 | ||||||
| chr13:101817598
|
T | C | 80 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(77): Show | 80 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.408+51127A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817598 | ||||||
| chr13:101817692
|
C | T | 1 | a0001c0001t0018g0221 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.408+51033G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817692 | ||||||
| chr13:101817744
|
G | A | 1 | a0001c0001t0060g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.408+50981C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101817744 | ||||||
| chr13:101818035
|
C | T | 1 | a0001c0001t0106g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.408+50690G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818035 | ||||||
| chr13:101818114
|
G | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+50611C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818114 | ||||||
| chr13:101818171
|
C | T | 5 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0067others(2): Show | 5 | NA18747.hp1 NA18960.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+50554G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818171 | ||||||
| chr13:101818425
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.408+50300G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818425 | ||||||
| chr13:101818479
|
T | C | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.408+50246A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818479 | ||||||
| chr13:101818623
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+50102G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818623 | ||||||
| chr13:101818726
|
T | A | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+49999A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818726 | ||||||
| chr13:101818981
|
C | A | 5 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0067others(2): Show | 5 | NA18747.hp1 NA18960.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+49744G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101818981 | ||||||
| chr13:101819065
|
ATACCCAG others(7): Show |
A | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+49646_408+4965 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819065 | ||||||
| chr13:101819100
|
C | G | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+49625G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819100 | ||||||
| chr13:101819160
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+49565C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819160 | ||||||
| chr13:101819412
|
A | C | 137 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.408+49313T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819412 | ||||||
| chr13:101819727
|
T | A | 1 | a0001c0001t0009g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.408+48998A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819727 | ||||||
| chr13:101819733
|
T | A | 135 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.408+48992A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819733 | ||||||
| chr13:101819750
|
A | C | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+48975T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819750 | ||||||
| chr13:101819769
|
A | G | 135 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.408+48956T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819769 | ||||||
| chr13:101819902
|
T | C | 37 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0009g0159others(34): Show | 37 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.408+48823A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819902 | ||||||
| chr13:101819921
|
T | C | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+48804A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819921 | ||||||
| chr13:101819957
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+48768T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101819957 | ||||||
| chr13:101820018
|
C | T | 75 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.408+48707G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820018 | ||||||
| chr13:101820197
|
T | C | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+48528A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820197 | ||||||
| chr13:101820253
|
A | C | 38 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(35): Show | 38 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.408+48472T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820253 | ||||||
| chr13:101820290
|
T | A | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+48435A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820290 | ||||||
| chr13:101820310
|
A | G | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0102g0138others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+48415T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820310 | ||||||
| chr13:101820327
|
T | C | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0066g0112 | 3 | HG03209.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.408+48398A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820327 | ||||||
| chr13:101820439
|
C | G | 18 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+48286G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820439 | ||||||
| chr13:101820487
|
C | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+48238G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820487 | ||||||
| chr13:101820723
|
A | T | 1 | a0001c0001t0041g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.408+48002T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820723 | ||||||
| chr13:101820755
|
A | AGAAAAGC others(56): Show |
4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47969_408+4797 others(67): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820755 | ||||||
| chr13:101820756
|
C | A | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47969G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820756 | ||||||
| chr13:101820756
|
C | G | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47969G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820756 | ||||||
| chr13:101820757
|
A | AAAAGCTA others(94): Show |
78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47967_408+4796 others(105): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820757 | ||||||
| chr13:101820758
|
G | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47967C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820758 | ||||||
| chr13:101820759
|
T | C | 5 | a0001c0001t0047g0165a0001c0001t0091g0117a0001c0001t0102g0138others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+47966A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820759 | ||||||
| chr13:101820759
|
T | TATA | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47965_408+4796 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820759 | ||||||
| chr13:101820761
|
C | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47964G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820761 | ||||||
| chr13:101820762
|
A | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47963T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820762 | ||||||
| chr13:101820763
|
C | G | 76 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.408+47962G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820763 | ||||||
| chr13:101820763
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47962G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820763 | ||||||
| chr13:101820764
|
A | C | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47961T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820764 | ||||||
| chr13:101820765
|
C | T | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47960G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820765 | ||||||
| chr13:101820768
|
AC | A | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47956delG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820768 | ||||||
| chr13:101820769
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47956G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820769 | ||||||
| chr13:101820770
|
A | G | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47955T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820770 | ||||||
| chr13:101820771
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47954G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820771 | ||||||
| chr13:101820771
|
CCACACAC others(8): Show |
C | 6 | a0001c0001t0016g0012a0001c0001t0028g0018a0001c0001t0028g0019others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+47939_408+4795 others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820771 | ||||||
| chr13:101820771
|
CCACACAC others(10): Show |
C | 59 | a0001c0001t0001g0051a0001c0001t0001g0132a0001c0001t0002g0055others(56): Show | 59 | HG00099.hp2 HG00597.hp2 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.408+47937_408+4795 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820771 | ||||||
| chr13:101820772
|
C | T | 82 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.408+47953G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820772 | ||||||
| chr13:101820772
|
CACACACC others(27): Show |
C | 18 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+47919_408+4795 others(38): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820772 | ||||||
| chr13:101820774
|
C | A | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47951G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820774 | ||||||
| chr13:101820776
|
C | G | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47949G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820776 | ||||||
| chr13:101820777
|
A | T | 82 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.408+47948T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820777 | ||||||
| chr13:101820778
|
C | A | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47947G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820778 | ||||||
| chr13:101820778
|
C | G | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47947G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820778 | ||||||
| chr13:101820778
|
CCACA | C | 4 | a0001c0001t0009g0159a0001c0001t0118g0242a0001c0001t0131g0162others(1): Show | 4 | HG02818.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+47943_408+4794 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820778 | ||||||
| chr13:101820780
|
A | C | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47945T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820780 | ||||||
| chr13:101820782
|
A | AAGTATTA others(10): Show |
4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47942_408+4794 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820782 | ||||||
| chr13:101820783
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47942G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820783 | ||||||
| chr13:101820787
|
C | G | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47938G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820787 | ||||||
| chr13:101820788
|
A | AC | 78 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.408+47936dupG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820788 | ||||||
| chr13:101820788
|
A | C | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47937T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820788 | ||||||
| chr13:101820789
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47936G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820789 | ||||||
| chr13:101820792
|
A | AG | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47932_408+4793 others(5): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820792 | ||||||
| chr13:101820793
|
C | T | 4 | a0001c0001t0008g0173a0001c0001t0012g0191a0001c0001t0033g0095others(1): Show | 4 | HG04184.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47932G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820793 | ||||||
| chr13:101820800
|
ACAC | A | 4 | a0001c0001t0001g0016a0001c0001t0017g0139a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47922_408+4792 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820800 | ||||||
| chr13:101820805
|
CA | C | 4 | a0001c0001t0001g0016a0001c0001t0017g0139a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+47919delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820805 | ||||||
| chr13:101820805
|
CAACA | C | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+47916_408+4791 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820805 | ||||||
| chr13:101820806
|
A | C | 134 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.408+47919T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820806 | ||||||
| chr13:101820874
|
A | T | 162 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.408+47851T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820874 | ||||||
| chr13:101820882
|
GCTT | G | 98 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(95): Show | 98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.408+47840_408+4784 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820882 | ||||||
| chr13:101820895
|
C | CCA | 162 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.408+47828_408+4782 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820895 | ||||||
| chr13:101820954
|
C | CT | 8 | a0001c0001t0001g0093a0001c0001t0016g0010a0001c0001t0027g0026others(5): Show | 8 | HG02145.hp2 HG02572.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+47770dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820954 | ||||||
| chr13:101820997
|
G | C | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+47728C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101820997 | ||||||
| chr13:101821000
|
T | A | 2 | a0001c0001t0049g0218a0001c0001t0103g0134 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.408+47725A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821000 | ||||||
| chr13:101821009
|
A | G | 176 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(173): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.408+47716T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821009 | ||||||
| chr13:101821010
|
T | C | 167 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(164): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.408+47715A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821010 | ||||||
| chr13:101821010
|
T | G | 9 | a0001c0001t0004g0088a0001c0001t0009g0203a0001c0001t0021g0210others(6): Show | 9 | HG00423.hp2 NA18948.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+47715A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821010 | ||||||
| chr13:101821028
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0020g0217 | 2 | NA18971.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.408+47697C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821028 | ||||||
| chr13:101821037
|
C | T | 4 | a0001c0001t0002g0109a0001c0001t0020g0217a0001c0001t0049g0218others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+47688G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821037 | ||||||
| chr13:101821044
|
A | G | 186 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.408+47681T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821044 | ||||||
| chr13:101821074
|
A | G | 106 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(103): Show | 106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.408+47651T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821074 | ||||||
| chr13:101821086
|
G | C | 167 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(164): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.408+47639C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821086 | ||||||
| chr13:101821100
|
T | C | 163 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.408+47625A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821100 | ||||||
| chr13:101821109
|
G | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+47616C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821109 | ||||||
| chr13:101821111
|
G | A | 2 | a0001c0001t0021g0170a0001c0001t0147g0220 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.408+47614C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821111 | ||||||
| chr13:101821131
|
G | A | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+47594C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821131 | ||||||
| chr13:101821157
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.408+47568G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821157 | ||||||
| chr13:101821165
|
T | G | 38 | a0001c0001t0001g0093a0001c0001t0001g0132a0001c0001t0006g0083others(35): Show | 38 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.408+47560A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821165 | ||||||
| chr13:101821289
|
G | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+47436C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821289 | ||||||
| chr13:101821327
|
T | C | 5 | a0001c0001t0017g0135a0001c0001t0050g0001a0001c0001t0121g0160others(2): Show | 5 | HG01081.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+47398A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821327 | ||||||
| chr13:101821465
|
C | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+47260G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821465 | ||||||
| chr13:101821471
|
G | C | 1 | a0001c0001t0085g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.408+47254C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821471 | ||||||
| chr13:101821843
|
T | C | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+46882A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821843 | ||||||
| chr13:101821859
|
A | T | 3 | a0001c0001t0080g0021a0001c0001t0082g0072a0001c0001t0129g0243 | 3 | HG01975.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.408+46866T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821859 | ||||||
| chr13:101821863
|
T | G | 3 | a0001c0001t0080g0021a0001c0001t0082g0072a0001c0001t0129g0243 | 3 | HG01975.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.408+46862A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821863 | ||||||
| chr13:101821918
|
G | A | 1 | a0001c0001t0008g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.408+46807C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101821918 | ||||||
| chr13:101822074
|
G | A | 1 | a0001c0001t0086g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.408+46651C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822074 | ||||||
| chr13:101822112
|
C | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+46613G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822112 | ||||||
| chr13:101822262
|
G | C | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+46463C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822262 | ||||||
| chr13:101822274
|
C | T | 1 | a0001c0001t0033g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.408+46451G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822274 | ||||||
| chr13:101822387
|
T | C | 165 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(162): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.408+46338A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822387 | ||||||
| chr13:101822494
|
CA | C | 142 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.408+46230delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822494 | ||||||
| chr13:101822494
|
CAA | C | 9 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+46229_408+4623 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822494 | ||||||
| chr13:101822521
|
C | T | 163 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.408+46204G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822521 | ||||||
| chr13:101822525
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0017g0139a0001c0001t0146g0156others(2): Show | 5 | HG01884.hp1 HG01993.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+46200G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822525 | ||||||
| chr13:101822565
|
T | A | 2 | a0001c0001t0051g0002a0001c0001t0061g0025 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+46160A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822565 | ||||||
| chr13:101822630
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.408+46095A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822630 | ||||||
| chr13:101822667
|
C | T | 23 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(20): Show | 23 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.408+46058G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822667 | ||||||
| chr13:101822679
|
G | A | 1 | a0001c0001t0145g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.408+46046C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822679 | ||||||
| chr13:101822684
|
A | G | 2 | a0001c0001t0023g0157a0001c0001t0023g0158 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.408+46041T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822684 | ||||||
| chr13:101822800
|
T | C | 1 | a0001c0001t0025g0008 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.408+45925A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822800 | ||||||
| chr13:101822934
|
C | T | 3 | a0001c0001t0010g0248a0001c0001t0010g0249a0001c0001t0124g0251 | 3 | HG00423.hp1 NA18951.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.408+45791G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101822934 | ||||||
| chr13:101823130
|
T | A | 1 | a0001c0001t0066g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.408+45595A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823130 | ||||||
| chr13:101823166
|
G | A | 10 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(7): Show | 10 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+45559C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823166 | ||||||
| chr13:101823209
|
T | C | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+45516A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823209 | ||||||
| chr13:101823227
|
T | A | 2 | a0001c0001t0015g0124a0001c0001t0110g0182 | 2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.408+45498A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823227 | ||||||
| chr13:101823275
|
C | CAG | 171 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(168): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.408+45449_408+4545 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823275 | ||||||
| chr13:101823300
|
C | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+45425G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823300 | ||||||
| chr13:101823532
|
G | C | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+45193C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823532 | ||||||
| chr13:101823626
|
G | A | 1 | a0001c0001t0005g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.408+45099C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823626 | ||||||
| chr13:101823807
|
A | T | 1 | a0001c0001t0066g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.408+44918T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823807 | ||||||
| chr13:101823858
|
A | T | 167 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(164): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.408+44867T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823858 | ||||||
| chr13:101823915
|
T | TAATC | 161 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.408+44809_408+4481 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101823915 | ||||||
| chr13:101824058
|
T | C | 1 | a0001c0001t0115g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.408+44667A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824058 | ||||||
| chr13:101824258
|
T | C | 161 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.408+44467A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824258 | ||||||
| chr13:101824336
|
C | T | 3 | a0001c0001t0009g0159a0001c0001t0131g0162a0001c0001t0157g0262 | 3 | HG02818.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.408+44389G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824336 | ||||||
| chr13:101824337
|
G | A | 1 | a0001c0001t0026g0027 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.408+44388C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824337 | ||||||
| chr13:101824369
|
T | A | 161 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.408+44356A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824369 | ||||||
| chr13:101824432
|
T | C | 185 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(182): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.408+44293A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824432 | ||||||
| chr13:101824724
|
A | G | 2 | a0001c0001t0075g0092a0001c0001t0120g0245 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.408+44001T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824724 | ||||||
| chr13:101824818
|
G | A | 183 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(180): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.408+43907C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824818 | ||||||
| chr13:101824898
|
A | G | 56 | a0001c0001t0001g0132a0001c0001t0003g0110a0001c0001t0006g0083others(53): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.408+43827T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824898 | ||||||
| chr13:101824909
|
C | A | 1 | a0001c0001t0118g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.408+43816G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824909 | ||||||
| chr13:101824963
|
G | T | 1 | a0001c0001t0101g0105 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.408+43762C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101824963 | ||||||
| chr13:101825019
|
T | C | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.408+43706A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825019 | ||||||
| chr13:101825097
|
T | C | 1 | a0001c0001t0060g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.408+43628A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825097 | ||||||
| chr13:101825285
|
T | G | 196 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(193): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.408+43440A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825285 | ||||||
| chr13:101825325
|
T | C | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+43400A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825325 | ||||||
| chr13:101825354
|
G | C | 1 | a0001c0001t0142g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.408+43371C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825354 | ||||||
| chr13:101825358
|
A | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+43367T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825358 | ||||||
| chr13:101825396
|
T | A | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+43329A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825396 | ||||||
| chr13:101825703
|
T | G | 24 | a0001c0001t0001g0132a0001c0001t0006g0083a0001c0001t0011g0235others(21): Show | 24 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.408+43022A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101825703 | ||||||
| chr13:101826093
|
C | T | 2 | a0001c0001t0029g0099a0001c0001t0039g0185 | 2 | NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.408+42632G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826093 | ||||||
| chr13:101826128
|
G | T | 183 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(180): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.408+42597C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826128 | ||||||
| chr13:101826230
|
A | G | 2 | a0001c0001t0021g0170a0001c0001t0147g0220 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.408+42495T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826230 | ||||||
| chr13:101826257
|
C | T | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+42468G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826257 | ||||||
| chr13:101826261
|
C | T | 1 | a0001c0001t0097g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.408+42464G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826261 | ||||||
| chr13:101826262
|
G | C | 3 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0068g0009 | 3 | HG03225.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+42463C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826262 | ||||||
| chr13:101826376
|
C | T | 17 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.408+42349G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826376 | ||||||
| chr13:101826382
|
T | G | 3 | a0001c0001t0007g0042a0001c0001t0007g0043a0001c0001t0087g0050 | 3 | HG01074.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.408+42343A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826382 | ||||||
| chr13:101826421
|
A | G | 2 | a0001c0001t0043g0253a0001c0001t0043g0254 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.408+42304T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826421 | ||||||
| chr13:101826538
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.408+42187G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826538 | ||||||
| chr13:101826539
|
G | A | 2 | a0001c0001t0028g0018a0001c0001t0028g0019 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.408+42186C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826539 | ||||||
| chr13:101826646
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+42079A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826646 | ||||||
| chr13:101826731
|
C | T | 30 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+41994G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826731 | ||||||
| chr13:101826780
|
C | G | 9 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+41945G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826780 | ||||||
| chr13:101826802
|
C | A | 1 | a0001c0001t0121g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.408+41923G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826802 | ||||||
| chr13:101826965
|
A | G | 11 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+41760T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101826965 | ||||||
| chr13:101827403
|
T | C | 1 | a0001c0001t0037g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.408+41322A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827403 | ||||||
| chr13:101827409
|
A | G | 27 | a0001c0001t0001g0132a0001c0001t0008g0233a0001c0001t0013g0142others(24): Show | 27 | HG01109.hp2 HG01192.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.408+41316T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827409 | ||||||
| chr13:101827498
|
C | A | 64 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0004g0088others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.408+41227G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827498 | ||||||
| chr13:101827811
|
G | A | 1 | a0001c0001t0012g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.408+40914C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827811 | ||||||
| chr13:101827844
|
T | A | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0022g0196 | 3 | NA18962.hp1 NA18992.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.408+40881A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827844 | ||||||
| chr13:101827921
|
T | A | 102 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(99): Show | 102 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.408+40804A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827921 | ||||||
| chr13:101827924
|
TA | T | 6 | a0001c0001t0017g0135a0001c0001t0023g0164a0001c0001t0047g0213others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+40800delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827924 | ||||||
| chr13:101827950
|
AG | A | 102 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(99): Show | 102 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.408+40774delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827950 | ||||||
| chr13:101827951
|
G | A | 12 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0135others(9): Show | 12 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+40774C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101827951 | ||||||
| chr13:101828113
|
C | T | 2 | a0001c0001t0016g0130a0001c0001t0161g0263 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.408+40612G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828113 | ||||||
| chr13:101828119
|
C | T | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+40606G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828119 | ||||||
| chr13:101828230
|
C | T | 159 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0132others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.408+40495G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828230 | ||||||
| chr13:101828409
|
A | C | 200 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(197): Show | 200 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.408+40316T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828409 | ||||||
| chr13:101828412
|
G | A | 3 | a0001c0001t0008g0152a0001c0001t0032g0060a0001c0001t0122g0193 | 3 | HG00323.hp2 HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.408+40313C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828412 | ||||||
| chr13:101828470
|
G | T | 2 | a0001c0001t0008g0208a0001c0001t0041g0209 | 2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.408+40255C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828470 | ||||||
| chr13:101828472
|
C | CT | 57 | a0001c0001t0001g0075a0001c0001t0002g0065a0001c0001t0002g0096others(54): Show | 57 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.408+40252dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828472 | ||||||
| chr13:101828472
|
C | CTT | 23 | a0001c0001t0008g0233a0001c0001t0013g0142a0001c0001t0013g0143others(20): Show | 23 | HG01109.hp2 HG01192.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.408+40251_408+4025 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828472 | ||||||
| chr13:101828472
|
CT | C | 16 | a0001c0001t0004g0057a0001c0001t0015g0114a0001c0001t0023g0157others(13): Show | 16 | HG01891.hp1 HG02258.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.408+40252delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828472 | ||||||
| chr13:101828518
|
T | C | 94 | a0001c0001t0001g0075a0001c0001t0001g0132a0001c0001t0002g0065others(91): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.408+40207A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828518 | ||||||
| chr13:101828594
|
G | C | 199 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(196): Show | 199 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.408+40131C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828594 | ||||||
| chr13:101828623
|
G | C | 199 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(196): Show | 199 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.408+40102C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828623 | ||||||
| chr13:101828628
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.408+40097G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828628 | ||||||
| chr13:101828763
|
T | C | 2 | a0001c0001t0017g0135a0001c0001t0050g0001 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.408+39962A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828763 | ||||||
| chr13:101828820
|
T | C | 3 | a0001c0001t0026g0027a0001c0001t0092g0113a0001c0001t0113g0234 | 3 | HG01255.hp2 HG01256.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.408+39905A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828820 | ||||||
| chr13:101828863
|
A | G | 1 | a0001c0001t0044g0252 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.408+39862T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828863 | ||||||
| chr13:101828874
|
T | C | 200 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(197): Show | 200 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.408+39851A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101828874 | ||||||
| chr13:101829031
|
T | C | 100 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.408+39694A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829031 | ||||||
| chr13:101829101
|
C | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+39624G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829101 | ||||||
| chr13:101829170
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+39555T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829170 | ||||||
| chr13:101829507
|
T | C | 8 | a0001c0001t0003g0110a0001c0001t0007g0081a0001c0001t0008g0152others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+39218A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829507 | ||||||
| chr13:101829676
|
C | T | 169 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0132others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.408+39049G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829676 | ||||||
| chr13:101829694
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.408+39031T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829694 | ||||||
| chr13:101829871
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.408+38854G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829871 | ||||||
| chr13:101829972
|
T | C | 5 | a0001c0001t0015g0121a0001c0001t0031g0035a0001c0001t0031g0108others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+38753A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101829972 | ||||||
| chr13:101830075
|
T | A | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.408+38650A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830075 | ||||||
| chr13:101830198
|
C | G | 1 | a0001c0001t0079g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.408+38527G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830198 | ||||||
| chr13:101830264
|
T | C | 6 | a0001c0001t0017g0135a0001c0001t0047g0213a0001c0001t0050g0001others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+38461A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830264 | ||||||
| chr13:101830268
|
C | T | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.408+38457G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830268 | ||||||
| chr13:101830370
|
T | C | 11 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+38355A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830370 | ||||||
| chr13:101830435
|
T | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+38290A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830435 | ||||||
| chr13:101830472
|
A | G | 2 | a0001c0001t0015g0114a0001c0001t0104g0137 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.408+38253T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830472 | ||||||
| chr13:101830638
|
T | A | 1 | a0001c0001t0069g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.408+38087A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830638 | ||||||
| chr13:101830782
|
T | C | 18 | a0001c0001t0008g0233a0001c0001t0013g0142a0001c0001t0013g0143others(15): Show | 18 | HG01109.hp2 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+37943A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830782 | ||||||
| chr13:101830893
|
C | G | 3 | a0001c0001t0026g0027a0001c0001t0092g0113a0001c0001t0113g0234 | 3 | HG01255.hp2 HG01256.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.408+37832G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830893 | ||||||
| chr13:101830928
|
C | A | 10 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+37797G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830928 | ||||||
| chr13:101830981
|
T | A | 1 | a0001c0001t0039g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.408+37744A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101830981 | ||||||
| chr13:101831186
|
G | A | 2 | a0001c0001t0017g0136a0001c0001t0121g0160 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.408+37539C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831186 | ||||||
| chr13:101831240
|
C | CTATT | 4 | a0001c0001t0018g0236a0001c0001t0080g0021a0001c0001t0112g0171others(1): Show | 4 | HG01081.hp2 HG03041.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+37481_408+3748 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831240 | ||||||
| chr13:101831240
|
CTATT | C | 43 | a0001c0001t0001g0029a0001c0001t0002g0055a0001c0001t0006g0073others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.408+37481_408+3748 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831240 | ||||||
| chr13:101831240
|
CTATTTAT others(1): Show |
C | 78 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0093others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.408+37477_408+3748 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831240 | ||||||
| chr13:101831240
|
CTATTTAT others(5): Show |
C | 19 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0002g0101others(16): Show | 19 | HG00408.hp1 HG00621.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.408+37473_408+3748 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831240 | ||||||
| chr13:101831450
|
C | G | 19 | a0001c0001t0008g0233a0001c0001t0013g0142a0001c0001t0013g0143others(16): Show | 19 | HG01109.hp2 HG01192.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.408+37275G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831450 | ||||||
| chr13:101831518
|
C | A | 1 | a0001c0001t0079g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.408+37207G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831518 | ||||||
| chr13:101831584
|
A | G | 1 | a0001c0001t0140g0192 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.408+37141T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831584 | ||||||
| chr13:101831602
|
A | T | 2 | a0001c0001t0061g0025a0001c0001t0093g0111 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+37123T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831602 | ||||||
| chr13:101831614
|
T | C | 2 | a0001c0001t0017g0135a0001c0001t0050g0001 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.408+37111A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831614 | ||||||
| chr13:101831637
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0093g0111 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+37088A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831637 | ||||||
| chr13:101831658
|
T | C | 2 | a0001c0001t0016g0012a0001c0001t0105g0133 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.408+37067A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831658 | ||||||
| chr13:101831744
|
G | C | 7 | a0001c0001t0013g0212a0001c0001t0017g0136a0001c0001t0019g0227others(4): Show | 7 | HG02630.hp1 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+36981C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831744 | ||||||
| chr13:101831867
|
G | A | 3 | a0001c0001t0010g0201a0001c0001t0011g0150a0001c0001t0155g0149 | 3 | HG02015.hp1 HG02559.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.408+36858C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831867 | ||||||
| chr13:101831898
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0135others(8): Show | 11 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.408+36827C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831898 | ||||||
| chr13:101831915
|
T | C | 2 | a0001c0001t0015g0114a0001c0001t0104g0137 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.408+36810A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831915 | ||||||
| chr13:101831917
|
G | C | 1 | a0001c0001t0159g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.408+36808C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831917 | ||||||
| chr13:101831998
|
C | T | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+36727G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101831998 | ||||||
| chr13:101832054
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0139others(4): Show | 7 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+36671C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832054 | ||||||
| chr13:101832109
|
G | A | 1 | a0001c0001t0024g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+36616C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832109 | ||||||
| chr13:101832132
|
G | A | 1 | a0001c0001t0031g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.408+36593C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832132 | ||||||
| chr13:101832175
|
T | C | 10 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+36550A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832175 | ||||||
| chr13:101832199
|
G | A | 1 | a0001c0001t0081g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+36526C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832199 | ||||||
| chr13:101832858
|
A | C | 1 | a0001c0001t0008g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.408+35867T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101832858 | ||||||
| chr13:101833128
|
G | C | 14 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0135others(11): Show | 14 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+35597C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101833128 | ||||||
| chr13:101833145
|
C | A | 61 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0004g0088others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.408+35580G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101833145 | ||||||
| chr13:101833173
|
C | T | 1 | a0001c0001t0011g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.408+35552G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101833173 | ||||||
| chr13:101833586
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.408+35139A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101833586 | ||||||
| chr13:101833588
|
T | C | 1 | a0001c0001t0027g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.408+35137A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101833588 | ||||||
| chr13:101834032
|
G | A | 11 | a0001c0001t0015g0114a0001c0001t0023g0157a0001c0001t0023g0158others(8): Show | 11 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+34693C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834032 | ||||||
| chr13:101834035
|
T | C | 10 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0024g0259others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+34690A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834035 | ||||||
| chr13:101834093
|
C | T | 211 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(208): Show | 211 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.408+34632G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834093 | ||||||
| chr13:101834121
|
T | G | 2 | a0001c0001t0061g0025a0001c0001t0093g0111 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+34604A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834121 | ||||||
| chr13:101834580
|
C | T | 13 | a0001c0001t0015g0114a0001c0001t0023g0157a0001c0001t0023g0158others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.408+34145G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834580 | ||||||
| chr13:101834765
|
A | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408+33960T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834765 | ||||||
| chr13:101834832
|
G | A | 1 | a0001c0001t0077g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.408+33893C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834832 | ||||||
| chr13:101834850
|
T | C | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.408+33875A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834850 | ||||||
| chr13:101834893
|
T | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408+33832A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101834893 | ||||||
| chr13:101835215
|
G | C | 59 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0002g0098others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.408+33510C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835215 | ||||||
| chr13:101835232
|
T | G | 1 | a0001c0001t0004g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.408+33493A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835232 | ||||||
| chr13:101835421
|
A | T | 198 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(195): Show | 198 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.408+33304T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835421 | ||||||
| chr13:101835514
|
A | T | 3 | a0001c0001t0078g0094a0001c0001t0115g0176a0001c0001t0126g0161 | 3 | HG02109.hp2 HG03831.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.408+33211T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835514 | ||||||
| chr13:101835573
|
G | T | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+33152C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835573 | ||||||
| chr13:101835641
|
A | T | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.408+33084T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835641 | ||||||
| chr13:101835937
|
C | T | 40 | a0001c0001t0004g0088a0001c0001t0006g0083a0001c0001t0009g0179others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.408+32788G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101835937 | ||||||
| chr13:101836025
|
T | A | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+32700A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836025 | ||||||
| chr13:101836160
|
G | C | 1 | a0001c0001t0081g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+32565C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836160 | ||||||
| chr13:101836391
|
A | C | 3 | a0001c0001t0007g0042a0001c0001t0007g0043a0001c0001t0087g0050 | 3 | HG01074.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.408+32334T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836391 | ||||||
| chr13:101836402
|
T | C | 17 | a0001c0001t0001g0132a0001c0001t0008g0233a0001c0001t0015g0114others(14): Show | 17 | HG01192.hp2 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.408+32323A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836402 | ||||||
| chr13:101836436
|
G | T | 1 | a0001c0001t0009g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.408+32289C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836436 | ||||||
| chr13:101836552
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+32173C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836552 | ||||||
| chr13:101836559
|
T | G | 4 | a0001c0001t0051g0002a0001c0001t0091g0117a0001c0001t0131g0162others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+32166A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836559 | ||||||
| chr13:101836615
|
C | T | 4 | a0001c0001t0019g0247a0001c0001t0080g0021a0001c0001t0082g0072others(1): Show | 4 | HG01975.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+32110G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836615 | ||||||
| chr13:101836627
|
G | A | 38 | a0001c0001t0004g0088a0001c0001t0006g0083a0001c0001t0009g0179others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.408+32098C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836627 | ||||||
| chr13:101836787
|
G | A | 68 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0004g0088others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.408+31938C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836787 | ||||||
| chr13:101836917
|
G | A | 2 | a0001c0001t0016g0010a0001c0001t0096g0129 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.408+31808C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101836917 | ||||||
| chr13:101837055
|
C | T | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.408+31670G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837055 | ||||||
| chr13:101837164
|
CTA | C | 23 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(20): Show | 23 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.408+31559_408+3156 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837164 | ||||||
| chr13:101837176
|
GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0020g0187a0001c0001t0040g0188a0001c0001t0040g0189others(1): Show | 4 | NA18941.hp2 NA18948.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+31541_408+3154 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837176 | ||||||
| chr13:101837413
|
A | T | 22 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.408+31312T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837413 | ||||||
| chr13:101837444
|
A | G | 1 | a0001c0001t0054g0004 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408+31281T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837444 | ||||||
| chr13:101837485
|
G | A | 5 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+31240C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837485 | ||||||
| chr13:101837489
|
T | C | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408+31236A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837489 | ||||||
| chr13:101837543
|
G | A | 2 | a0001c0001t0026g0027a0001c0001t0092g0113 | 2 | HG01256.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.408+31182C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837543 | ||||||
| chr13:101837564
|
T | C | 1 | a0001c0001t0003g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.408+31161A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837564 | ||||||
| chr13:101837684
|
C | T | 38 | a0001c0001t0004g0088a0001c0001t0006g0083a0001c0001t0009g0179others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.408+31041G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837684 | ||||||
| chr13:101837690
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.408+31035A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837690 | ||||||
| chr13:101837868
|
T | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.408+30857A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837868 | ||||||
| chr13:101837980
|
C | T | 3 | a0001c0001t0037g0066a0001c0001t0038g0125a0001c0001t0071g0128 | 3 | HG01175.hp1 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.408+30745G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837980 | ||||||
| chr13:101837996
|
C | G | 11 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0013g0142others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.408+30729G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101837996 | ||||||
| chr13:101838049
|
C | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+30676G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101838049 | ||||||
| chr13:101838695
|
T | C | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+30030A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101838695 | ||||||
| chr13:101838988
|
A | G | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+29737T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101838988 | ||||||
| chr13:101839079
|
C | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+29646G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839079 | ||||||
| chr13:101839170
|
G | A | 4 | a0001c0001t0019g0227a0001c0001t0024g0259a0001c0001t0024g0260others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+29555C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839170 | ||||||
| chr13:101839279
|
A | G | 3 | a0001c0002t0014g0118a0001c0002t0127g0224a0001c0002t0128g0155 | 3 | HG01192.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.408+29446T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839279 | ||||||
| chr13:101839439
|
A | G | 1 | a0001c0001t0159g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.408+29286T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839439 | ||||||
| chr13:101839547
|
G | C | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+29178C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839547 | ||||||
| chr13:101839822
|
T | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.408+28903A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839822 | ||||||
| chr13:101839882
|
G | A | 77 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0004g0088others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.408+28843C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839882 | ||||||
| chr13:101839901
|
C | T | 1 | a0001c0001t0004g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.408+28824G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839901 | ||||||
| chr13:101839954
|
C | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+28771G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101839954 | ||||||
| chr13:101840125
|
A | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+28600T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840125 | ||||||
| chr13:101840137
|
C | T | 4 | a0001c0001t0019g0227a0001c0001t0024g0259a0001c0001t0024g0260others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+28588G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840137 | ||||||
| chr13:101840475
|
T | G | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+28250A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840475 | ||||||
| chr13:101840606
|
C | A | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.408+28119G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840606 | ||||||
| chr13:101840624
|
G | C | 1 | a0001c0001t0103g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408+28101C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840624 | ||||||
| chr13:101840746
|
T | C | 1 | a0001c0001t0019g0227 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408+27979A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840746 | ||||||
| chr13:101840804
|
G | C | 1 | a0001c0001t0020g0187 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.408+27921C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840804 | ||||||
| chr13:101840873
|
A | G | 214 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(211): Show | 214 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.408+27852T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101840873 | ||||||
| chr13:101841068
|
G | T | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+27657C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841068 | ||||||
| chr13:101841211
|
T | C | 106 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(103): Show | 106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.408+27514A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841211 | ||||||
| chr13:101841259
|
A | G | 9 | a0001c0001t0016g0130a0001c0001t0023g0157a0001c0001t0023g0158others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.408+27466T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841259 | ||||||
| chr13:101841326
|
G | A | 49 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0002g0098others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.408+27399C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841326 | ||||||
| chr13:101841431
|
G | C | 13 | a0001c0001t0008g0233a0001c0001t0015g0114a0001c0001t0023g0164others(10): Show | 13 | HG01192.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+27294C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841431 | ||||||
| chr13:101841568
|
C | T | 3 | a0001c0001t0009g0241a0001c0001t0150g0146a0001c0001t0158g0264 | 3 | HG01081.hp2 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.408+27157G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841568 | ||||||
| chr13:101841575
|
G | T | 1 | a0001c0001t0023g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.408+27150C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841575 | ||||||
| chr13:101841645
|
C | T | 10 | a0001c0001t0016g0130a0001c0001t0023g0157a0001c0001t0023g0158others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+27080G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841645 | ||||||
| chr13:101841720
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+27005C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841720 | ||||||
| chr13:101841799
|
G | A | 49 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0002g0098others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.408+26926C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841799 | ||||||
| chr13:101841887
|
T | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+26838A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841887 | ||||||
| chr13:101841944
|
T | C | 25 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.408+26781A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101841944 | ||||||
| chr13:101842038
|
G | A | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+26687C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842038 | ||||||
| chr13:101842119
|
G | C | 1 | a0001c0001t0056g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.408+26606C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842119 | ||||||
| chr13:101842141
|
T | C | 82 | a0001c0001t0001g0132a0001c0001t0002g0065a0001c0001t0002g0096others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.408+26584A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842141 | ||||||
| chr13:101842189
|
T | C | 10 | a0001c0001t0016g0130a0001c0001t0023g0157a0001c0001t0023g0158others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+26536A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842189 | ||||||
| chr13:101842230
|
G | T | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.408+26495C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842230 | ||||||
| chr13:101842398
|
C | T | 1 | a0001c0001t0013g0142 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.408+26327G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842398 | ||||||
| chr13:101842485
|
G | C | 10 | a0001c0001t0016g0130a0001c0001t0023g0157a0001c0001t0023g0158others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+26240C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842485 | ||||||
| chr13:101842732
|
A | G | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0046g0169others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+25993T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842732 | ||||||
| chr13:101842804
|
A | G | 4 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0046g0169others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+25921T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842804 | ||||||
| chr13:101842887
|
C | G | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+25838G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842887 | ||||||
| chr13:101842952
|
C | T | 2 | a0001c0001t0137g0240a0001c0001t0143g0239 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.408+25773G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842952 | ||||||
| chr13:101842975
|
T | C | 1 | a0001c0001t0060g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.408+25750A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101842975 | ||||||
| chr13:101843103
|
G | A | 177 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0055others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.408+25622C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843103 | ||||||
| chr13:101843302
|
G | T | 35 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(32): Show | 35 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.408+25423C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843302 | ||||||
| chr13:101843388
|
G | A | 13 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0013g0142others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.408+25337C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843388 | ||||||
| chr13:101843486
|
G | A | 2 | a0001c0001t0008g0208a0001c0001t0041g0209 | 2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.408+25239C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843486 | ||||||
| chr13:101843789
|
G | A | 10 | a0001c0001t0016g0130a0001c0001t0023g0157a0001c0001t0023g0158others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+24936C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843789 | ||||||
| chr13:101843812
|
T | C | 29 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.408+24913A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843812 | ||||||
| chr13:101843818
|
G | A | 15 | a0001c0001t0006g0083a0001c0001t0011g0235a0001c0001t0016g0010others(12): Show | 15 | HG00099.hp2 HG01106.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.408+24907C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101843818 | ||||||
| chr13:101844100
|
T | G | 1 | a0001c0001t0085g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.408+24625A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101844100 | ||||||
| chr13:101844527
|
A | C | 6 | a0001c0001t0017g0135a0001c0001t0047g0213a0001c0001t0050g0001others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+24198T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101844527 | ||||||
| chr13:101844696
|
T | C | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.408+24029A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101844696 | ||||||
| chr13:101844760
|
G | A | 1 | a0001c0001t0015g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.408+23965C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101844760 | ||||||
| chr13:101845077
|
G | A | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.408+23648C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845077 | ||||||
| chr13:101845104
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.408+23621C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845104 | ||||||
| chr13:101845119
|
A | T | 4 | a0001c0001t0049g0218a0001c0001t0095g0022a0001c0001t0103g0134others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+23606T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845119 | ||||||
| chr13:101845328
|
A | T | 225 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(222): Show | 225 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.408+23397T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845328 | ||||||
| chr13:101845341
|
C | G | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+23384G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845341 | ||||||
| chr13:101845592
|
A | G | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+23133T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845592 | ||||||
| chr13:101845703
|
C | T | 50 | a0001c0001t0001g0075a0001c0001t0002g0065a0001c0001t0002g0096others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.408+23022G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845703 | ||||||
| chr13:101845924
|
AGTGAACA others(160): Show |
A | 1 | a0001c0001t0054g0004 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408+22634_408+2280 others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845924 | ||||||
| chr13:101845940
|
C | T | 4 | a0001c0001t0056g0107a0001c0001t0133g0211a0001c0001t0134g0180others(1): Show | 4 | HG01496.hp2 HG01943.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+22785G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845940 | ||||||
| chr13:101845985
|
A | G | 47 | a0001c0001t0001g0016a0001c0001t0003g0110a0001c0001t0007g0081others(44): Show | 47 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.408+22740T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101845985 | ||||||
| chr13:101846048
|
G | A | 48 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0002g0098others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.408+22677C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846048 | ||||||
| chr13:101846054
|
G | T | 4 | a0001c0001t0012g0216a0001c0001t0017g0135a0001c0001t0050g0001others(1): Show | 4 | HG02451.hp1 HG02523.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+22671C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846054 | ||||||
| chr13:101846093
|
C | A | 1 | a0001c0001t0054g0004 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.408+22632G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846093 | ||||||
| chr13:101846282
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.408+22443A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846282 | ||||||
| chr13:101846312
|
A | T | 1 | a0001c0001t0065g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.408+22413T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846312 | ||||||
| chr13:101846335
|
T | C | 2 | a0001c0001t0035g0044a0001c0001t0077g0041 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.408+22390A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846335 | ||||||
| chr13:101846379
|
T | C | 3 | a0001c0001t0009g0159a0001c0001t0009g0241a0001c0001t0161g0263 | 3 | HG02145.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.408+22346A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846379 | ||||||
| chr13:101846502
|
C | T | 2 | a0001c0001t0150g0146a0001c0001t0158g0264 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.408+22223G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846502 | ||||||
| chr13:101846618
|
C | T | 3 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0158g0264 | 3 | HG01081.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.408+22107G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846618 | ||||||
| chr13:101846697
|
T | G | 1 | a0001c0001t0019g0227 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408+22028A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846697 | ||||||
| chr13:101846960
|
C | A | 14 | a0001c0001t0003g0058a0001c0001t0007g0081a0001c0001t0008g0152others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.408+21765G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101846960 | ||||||
| chr13:101847189
|
T | G | 198 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.408+21536A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847189 | ||||||
| chr13:101847238
|
A | G | 1 | a0001c0001t0104g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.408+21487T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847238 | ||||||
| chr13:101847244
|
G | C | 7 | a0001c0001t0019g0244a0001c0001t0023g0164a0001c0001t0079g0013others(4): Show | 7 | HG01192.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+21481C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847244 | ||||||
| chr13:101847287
|
T | C | 4 | a0001c0001t0013g0143a0001c0001t0013g0144a0001c0001t0015g0114others(1): Show | 4 | HG01109.hp2 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+21438A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847287 | ||||||
| chr13:101847398
|
T | C | 3 | a0001c0001t0008g0208a0001c0001t0041g0209a0001c0001t0142g0228 | 3 | NA18977.hp1 NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.408+21327A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847398 | ||||||
| chr13:101847428
|
A | T | 20 | a0001c0001t0001g0016a0001c0001t0003g0058a0001c0001t0007g0081others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.408+21297T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847428 | ||||||
| chr13:101847486
|
A | G | 2 | a0001c0001t0068g0009a0001c0001t0147g0220 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+21239T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847486 | ||||||
| chr13:101847526
|
G | A | 1 | a0001c0001t0021g0210 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.408+21199C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847526 | ||||||
| chr13:101847592
|
T | C | 4 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0047g0165others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+21133A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847592 | ||||||
| chr13:101847605
|
T | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+21120A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847605 | ||||||
| chr13:101847697
|
C | T | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+21028G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847697 | ||||||
| chr13:101847710
|
A | G | 1 | a0001c0001t0046g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.408+21015T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847710 | ||||||
| chr13:101847755
|
T | G | 2 | a0001c0001t0018g0236a0001c0001t0032g0060 | 2 | HG01433.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.408+20970A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847755 | ||||||
| chr13:101847917
|
G | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+20808C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101847917 | ||||||
| chr13:101848004
|
G | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+20721C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848004 | ||||||
| chr13:101848039
|
T | C | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+20686A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848039 | ||||||
| chr13:101848150
|
A | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+20575T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848150 | ||||||
| chr13:101848276
|
C | T | 2 | a0001c0001t0061g0025a0001c0001t0157g0262 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408+20449G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848276 | ||||||
| chr13:101848336
|
C | G | 87 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(84): Show | 87 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.408+20389G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848336 | ||||||
| chr13:101848516
|
T | G | 1 | a0001c0002t0014g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.408+20209A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848516 | ||||||
| chr13:101848560
|
T | G | 1 | a0001c0001t0073g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.408+20165A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848560 | ||||||
| chr13:101848573
|
G | A | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+20152C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848573 | ||||||
| chr13:101848639
|
T | C | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.408+20086A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848639 | ||||||
| chr13:101848777
|
T | C | 1 | a0001c0001t0005g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.408+19948A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848777 | ||||||
| chr13:101848973
|
T | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+19752A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848973 | ||||||
| chr13:101848998
|
T | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+19727A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101848998 | ||||||
| chr13:101849292
|
G | A | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.408+19433C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849292 | ||||||
| chr13:101849517
|
C | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+19208G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849517 | ||||||
| chr13:101849560
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0136others(31): Show | 34 | HG01192.hp2 HG01884.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.408+19165C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849560 | ||||||
| chr13:101849569
|
A | G | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+19156T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849569 | ||||||
| chr13:101849678
|
G | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+19047C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849678 | ||||||
| chr13:101849759
|
T | G | 1 | a0001c0001t0092g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.408+18966A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101849759 | ||||||
| chr13:101850043
|
A | G | 1 | a0001c0001t0097g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.408+18682T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850043 | ||||||
| chr13:101850277
|
T | TA | 10 | a0001c0001t0009g0203a0001c0001t0017g0136a0001c0001t0079g0013others(7): Show | 10 | HG00423.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+18447_408+1844 others(5): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850277 | ||||||
| chr13:101850277
|
TCC | T | 36 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(33): Show | 36 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.408+18446_408+1844 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850277 | ||||||
| chr13:101850277
|
TCCAAAAA others(1): Show |
T | 14 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(11): Show | 14 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.408+18440_408+1844 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850277 | ||||||
| chr13:101850277
|
TCCAAAAA others(2): Show |
T | 22 | a0001c0001t0003g0076a0001c0001t0008g0233a0001c0001t0018g0221others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.408+18439_408+1844 others(13): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850277 | ||||||
| chr13:101850277
|
TCCAAAAA others(3): Show |
T | 1 | a0001c0001t0017g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.408+18438_408+1844 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850277 | ||||||
| chr13:101850278
|
C | A | 180 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0093others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.408+18447G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850278 | ||||||
| chr13:101850279
|
C | A | 10 | a0001c0001t0009g0203a0001c0001t0017g0136a0001c0001t0079g0013others(7): Show | 10 | HG00423.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+18446G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850279 | ||||||
| chr13:101850279
|
CA | C | 118 | a0001c0001t0001g0033a0001c0001t0001g0093a0001c0001t0002g0055others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.408+18445delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850279 | ||||||
| chr13:101850281
|
A | C | 36 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(33): Show | 36 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.408+18444T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850281 | ||||||
| chr13:101850282
|
A | C | 1 | a0001c0001t0056g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.408+18443T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850282 | ||||||
| chr13:101850286
|
A | C | 1 | a0001c0001t0095g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.408+18439T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850286 | ||||||
| chr13:101850287
|
A | C | 15 | a0001c0001t0001g0132a0001c0001t0002g0055a0001c0001t0013g0212others(12): Show | 15 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.408+18438T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850287 | ||||||
| chr13:101850288
|
A | C | 22 | a0001c0001t0003g0076a0001c0001t0008g0233a0001c0001t0018g0221others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.408+18437T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850288 | ||||||
| chr13:101850289
|
A | C | 1 | a0001c0001t0017g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.408+18436T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850289 | ||||||
| chr13:101850290
|
A | C | 1 | a0001c0001t0002g0055 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.408+18435T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850290 | ||||||
| chr13:101850311
|
G | A | 1 | a0001c0001t0141g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.408+18414C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850311 | ||||||
| chr13:101850333
|
T | A | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18392A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850333 | ||||||
| chr13:101850359
|
T | C | 1 | a0001c0001t0041g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.408+18366A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850359 | ||||||
| chr13:101850461
|
AATATATA others(60): Show |
A | 5 | a0001c0001t0073g0045a0001c0001t0133g0211a0001c0001t0134g0180others(2): Show | 5 | HG01496.hp2 HG01934.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+18197_408+1826 others(71): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850461 | ||||||
| chr13:101850462
|
ATATATAT others(58): Show |
A | 1 | a0001c0001t0144g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.408+18198_408+1826 others(69): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850462 | ||||||
| chr13:101850464
|
ATATATAT others(56): Show |
A | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+18198_408+1826 others(67): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850464 | ||||||
| chr13:101850466
|
ATATATAT others(54): Show |
A | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.408+18198_408+1825 others(65): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850466 | ||||||
| chr13:101850472
|
ATATATAT others(48): Show |
A | 1 | a0001c0001t0106g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.408+18198_408+1825 others(59): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850472 | ||||||
| chr13:101850474
|
ATATATAT others(46): Show |
A | 1 | a0001c0001t0130g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.408+18198_408+1825 others(57): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850474 | ||||||
| chr13:101850476
|
ATATATAT others(44): Show |
A | 1 | a0001c0001t0098g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.408+18198_408+1824 others(55): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850476 | ||||||
| chr13:101850477
|
TATATATA others(55): Show |
T | 2 | a0001c0001t0002g0096a0001c0001t0116g0246 | 2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.408+18186_408+1824 others(66): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850477 | ||||||
| chr13:101850478
|
ATATATAT others(42): Show |
A | 7 | a0001c0001t0003g0076a0001c0001t0020g0187a0001c0001t0055g0006others(4): Show | 7 | HG00408.hp2 HG01255.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+18198_408+1824 others(53): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850478 | ||||||
| chr13:101850480
|
ATATATAT others(40): Show |
A | 12 | a0001c0001t0007g0081a0001c0001t0021g0210a0001c0001t0040g0188others(9): Show | 12 | HG00280.hp2 HG01928.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.408+18198_408+1824 others(51): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850480 | ||||||
| chr13:101850482
|
ATATATAT others(38): Show |
A | 14 | a0001c0001t0004g0088a0001c0001t0008g0152a0001c0001t0009g0203others(11): Show | 14 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.408+18198_408+1824 others(49): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850482 | ||||||
| chr13:101850483
|
TATATATA others(49): Show |
T | 9 | a0001c0001t0050g0001a0001c0001t0051g0002a0001c0001t0081g0120others(6): Show | 9 | HG01884.hp2 HG01975.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.408+18186_408+1824 others(60): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850483 | ||||||
| chr13:101850484
|
ATATATAT others(36): Show |
A | 8 | a0001c0001t0009g0179a0001c0001t0012g0191a0001c0001t0012g0230others(5): Show | 8 | HG00438.hp1 HG00544.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+18198_408+1824 others(47): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850484 | ||||||
| chr13:101850485
|
TATATATA others(47): Show |
T | 11 | a0001c0001t0001g0016a0001c0001t0019g0227a0001c0001t0023g0157others(8): Show | 11 | HG01433.hp1 HG01884.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.408+18186_408+1823 others(58): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850485 | ||||||
| chr13:101850486
|
A | C | 2 | a0001c0001t0057g0086a0001c0001t0159g0257 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.408+18239T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850486 | ||||||
| chr13:101850486
|
ATATATAT others(34): Show |
A | 5 | a0001c0001t0008g0173a0001c0001t0036g0061a0001c0001t0036g0062others(2): Show | 5 | HG03490.hp1 HG03492.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+18198_408+1823 others(45): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850486 | ||||||
| chr13:101850487
|
TATATATA others(45): Show |
T | 3 | a0001c0001t0009g0159a0001c0001t0046g0169a0001c0001t0121g0160 | 3 | HG03139.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.408+18186_408+1823 others(56): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850487 | ||||||
| chr13:101850490
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0161g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.408+18207_408+1823 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850490 | ||||||
| chr13:101850490
|
ATATATAT others(30): Show |
A | 3 | a0001c0001t0022g0195a0001c0001t0022g0196a0001c0001t0107g0175 | 3 | HG00280.hp1 NA18962.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.408+18198_408+1823 others(41): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850490 | ||||||
| chr13:101850491
|
TATATATA others(41): Show |
T | 8 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0005g0047others(5): Show | 8 | HG00597.hp2 NA18948.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+18186_408+1823 others(52): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850491 | ||||||
| chr13:101850491
|
TATATATA others(45): Show |
T | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+18182_408+1823 others(56): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850491 | ||||||
| chr13:101850492
|
ATATATAT others(28): Show |
A | 4 | a0001c0001t0022g0194a0001c0001t0031g0108a0001c0001t0044g0178others(1): Show | 4 | HG00099.hp1 HG03831.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+18198_408+1823 others(39): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850492 | ||||||
| chr13:101850493
|
TATATATA others(39): Show |
T | 1 | a0001c0001t0074g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.408+18186_408+1823 others(50): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850493 | ||||||
| chr13:101850494
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0035g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.408+18207_408+1823 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850494 | ||||||
| chr13:101850495
|
TATATATA others(37): Show |
T | 2 | a0001c0001t0006g0097a0001c0001t0085g0063 | 2 | HG00323.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.408+18186_408+1822 others(48): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850495 | ||||||
| chr13:101850499
|
TATATATA others(33): Show |
T | 5 | a0001c0001t0003g0110a0001c0001t0016g0010a0001c0001t0025g0007others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+18186_408+1822 others(44): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850499 | ||||||
| chr13:101850500
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0160g0258 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.408+18207_408+1822 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850500 | ||||||
| chr13:101850501
|
TATATATA others(31): Show |
T | 19 | a0001c0001t0001g0036a0001c0001t0003g0106a0001c0001t0004g0082others(16): Show | 19 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.408+18186_408+1822 others(42): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850501 | ||||||
| chr13:101850502
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.408+18207_408+1822 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850502 | ||||||
| chr13:101850503
|
TATATATA others(29): Show |
T | 35 | a0001c0001t0001g0033a0001c0001t0001g0093a0001c0001t0002g0055others(32): Show | 35 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.408+18186_408+1822 others(40): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850503 | ||||||
| chr13:101850505
|
TATATATA others(27): Show |
T | 47 | a0001c0001t0001g0051a0001c0001t0001g0075a0001c0001t0001g0132others(44): Show | 47 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.408+18186_408+1821 others(38): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850505 | ||||||
| chr13:101850505
|
TATATATA others(40): Show |
T | 1 | a0001c0001t0103g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408+18173_408+1821 others(51): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850505 | ||||||
| chr13:101850507
|
TATATATA others(25): Show |
T | 21 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0002g0065others(18): Show | 21 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.408+18186_408+1821 others(36): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850507 | ||||||
| chr13:101850507
|
TATATATA others(38): Show |
T | 1 | a0001c0001t0008g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.408+18173_408+1821 others(49): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850507 | ||||||
| chr13:101850509
|
TATATAGA others(23): Show |
T | 14 | a0001c0001t0003g0058a0001c0001t0004g0057a0001c0001t0004g0078others(11): Show | 14 | HG01099.hp1 HG01099.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+18186_408+1821 others(34): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850509 | ||||||
| chr13:101850509
|
TATATAGA others(36): Show |
T | 1 | a0001c0001t0049g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.408+18173_408+1821 others(47): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850509 | ||||||
| chr13:101850511
|
TATAGAAT others(21): Show |
T | 11 | a0001c0001t0006g0059a0001c0001t0008g0208a0001c0001t0020g0250others(8): Show | 11 | HG00544.hp2 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+18186_408+1821 others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850511 | ||||||
| chr13:101850513
|
TAGAATTA others(19): Show |
T | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.408+18186_408+1821 others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850513 | ||||||
| chr13:101850514
|
AGAATTAT others(17): Show |
A | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+18187_408+1821 others(28): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850514 | ||||||
| chr13:101850526
|
T | G | 4 | a0001c0001t0035g0089a0001c0001t0131g0162a0001c0001t0160g0258others(1): Show | 4 | HG02145.hp1 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+18199A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850526 | ||||||
| chr13:101850536
|
TATA | T | 3 | a0001c0001t0131g0162a0001c0001t0160g0258a0001c0001t0161g0263 | 3 | HG02145.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.408+18186_408+1818 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850536 | ||||||
| chr13:101850539
|
A | T | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+18186T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850539 | ||||||
| chr13:101850540
|
T | G | 194 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(191): Show | 194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.408+18185A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850540 | ||||||
| chr13:101850541
|
A | C | 194 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(191): Show | 194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.408+18184T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850541 | ||||||
| chr13:101850599
|
T | A | 1 | a0001c0001t0017g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.408+18126A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850599 | ||||||
| chr13:101850604
|
T | C | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+18121A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850604 | ||||||
| chr13:101850617
|
T | C | 31 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0017g0136others(28): Show | 31 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.408+18108A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850617 | ||||||
| chr13:101850663
|
A | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18062T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850663 | ||||||
| chr13:101850664
|
T | C | 1 | a0001c0001t0109g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.408+18061A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850664 | ||||||
| chr13:101850668
|
G | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18057C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850668 | ||||||
| chr13:101850670
|
G | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18055C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850670 | ||||||
| chr13:101850671
|
A | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18054T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850671 | ||||||
| chr13:101850672
|
A | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18053T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850672 | ||||||
| chr13:101850676
|
A | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18049T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850676 | ||||||
| chr13:101850680
|
T | G | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18045A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850680 | ||||||
| chr13:101850682
|
T | A | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+18043A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850682 | ||||||
| chr13:101850721
|
G | T | 111 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0055others(108): Show | 111 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.408+18004C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101850721 | ||||||
| chr13:101851209
|
C | T | 2 | a0001c0001t0107g0175a0001c0001t0145g0174 | 2 | HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.408+17516G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851209 | ||||||
| chr13:101851221
|
C | T | 1 | a0001c0001t0019g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.408+17504G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851221 | ||||||
| chr13:101851237
|
T | C | 1 | a0001c0001t0018g0221 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.408+17488A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851237 | ||||||
| chr13:101851457
|
C | T | 14 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+17268G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851457 | ||||||
| chr13:101851572
|
T | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+17153A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851572 | ||||||
| chr13:101851635
|
C | T | 1 | a0001c0001t0048g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.408+17090G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851635 | ||||||
| chr13:101851683
|
C | T | 1 | a0001c0001t0139g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.408+17042G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101851683 | ||||||
| chr13:101852452
|
C | T | 1 | a0001c0001t0123g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.408+16273G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101852452 | ||||||
| chr13:101852560
|
T | C | 23 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0019g0227others(20): Show | 23 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.408+16165A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101852560 | ||||||
| chr13:101852594
|
T | TA | 60 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(57): Show | 60 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.408+16130dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101852594 | ||||||
| chr13:101852649
|
A | G | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+16076T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101852649 | ||||||
| chr13:101852910
|
C | A | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+15815G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101852910 | ||||||
| chr13:101853114
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.408+15611A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853114 | ||||||
| chr13:101853126
|
A | T | 45 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(42): Show | 45 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.408+15599T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853126 | ||||||
| chr13:101853233
|
C | T | 1 | a0001c0001t0004g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.408+15492G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853233 | ||||||
| chr13:101853494
|
C | T | 3 | a0001c0001t0010g0201a0001c0001t0011g0150a0001c0001t0155g0149 | 3 | HG02015.hp1 HG02559.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.408+15231G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853494 | ||||||
| chr13:101853648
|
G | T | 98 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.408+15077C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853648 | ||||||
| chr13:101853684
|
A | G | 46 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(43): Show | 46 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.408+15041T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853684 | ||||||
| chr13:101853692
|
G | A | 45 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(42): Show | 45 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.408+15033C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853692 | ||||||
| chr13:101853756
|
A | G | 1 | a0001c0001t0012g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.408+14969T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853756 | ||||||
| chr13:101853833
|
T | G | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+14892A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853833 | ||||||
| chr13:101853884
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+14841C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101853884 | ||||||
| chr13:101854097
|
G | A | 45 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(42): Show | 45 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.408+14628C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854097 | ||||||
| chr13:101854157
|
C | A | 5 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+14568G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854157 | ||||||
| chr13:101854158
|
G | A | 1 | a0001c0001t0112g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.408+14567C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854158 | ||||||
| chr13:101854160
|
A | G | 1 | a0001c0001t0026g0027 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.408+14565T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854160 | ||||||
| chr13:101854184
|
G | T | 45 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(42): Show | 45 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.408+14541C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854184 | ||||||
| chr13:101854243
|
T | A | 193 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(190): Show | 193 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.408+14482A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854243 | ||||||
| chr13:101854571
|
C | T | 14 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+14154G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854571 | ||||||
| chr13:101854633
|
G | A | 3 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243 | 3 | HG02970.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.408+14092C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854633 | ||||||
| chr13:101854636
|
A | G | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+14089T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101854636 | ||||||
| chr13:101855314
|
G | C | 2 | a0001c0001t0023g0157a0001c0001t0023g0158 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.408+13411C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855314 | ||||||
| chr13:101855501
|
C | T | 98 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.408+13224G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855501 | ||||||
| chr13:101855572
|
C | A | 97 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(94): Show | 97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.408+13153G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855572 | ||||||
| chr13:101855833
|
T | C | 1 | a0001c0001t0125g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.408+12892A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855833 | ||||||
| chr13:101855836
|
T | C | 3 | a0001c0001t0131g0162a0001c0001t0160g0258a0001c0001t0161g0263 | 3 | HG02145.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.408+12889A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855836 | ||||||
| chr13:101855897
|
C | T | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+12828G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855897 | ||||||
| chr13:101855899
|
A | G | 100 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(97): Show | 100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.408+12826T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855899 | ||||||
| chr13:101855903
|
G | GT | 148 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(145): Show | 148 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.408+12821dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855903 | ||||||
| chr13:101855903
|
G | GTT | 47 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(44): Show | 47 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.408+12820_408+1282 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101855903 | ||||||
| chr13:101856063
|
G | A | 195 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(192): Show | 195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.408+12662C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856063 | ||||||
| chr13:101856535
|
C | A | 14 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+12190G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856535 | ||||||
| chr13:101856654
|
A | G | 1 | a0001c0001t0042g0231 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.408+12071T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856654 | ||||||
| chr13:101856765
|
C | T | 5 | a0001c0001t0017g0136a0001c0001t0079g0013a0001c0001t0102g0138others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+11960G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856765 | ||||||
| chr13:101856871
|
G | T | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.408+11854C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856871 | ||||||
| chr13:101856966
|
G | T | 98 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.408+11759C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856966 | ||||||
| chr13:101856970
|
A | C | 3 | a0001c0001t0051g0002a0001c0001t0092g0113a0001c0001t0151g0147 | 3 | HG02109.hp1 HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.408+11755T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101856970 | ||||||
| chr13:101857224
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0066g0112others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+11501C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857224 | ||||||
| chr13:101857388
|
T | C | 157 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(154): Show | 157 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.408+11337A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857388 | ||||||
| chr13:101857651
|
A | C | 207 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(204): Show | 207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.408+11074T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857651 | ||||||
| chr13:101857708
|
A | G | 46 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0030others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.408+11017T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857708 | ||||||
| chr13:101857712
|
T | A | 46 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0030others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.408+11013A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857712 | ||||||
| chr13:101857780
|
C | A | 100 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(97): Show | 100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.408+10945G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857780 | ||||||
| chr13:101857816
|
A | G | 160 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(157): Show | 160 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.408+10909T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857816 | ||||||
| chr13:101857843
|
T | C | 60 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0051others(57): Show | 60 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.408+10882A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857843 | ||||||
| chr13:101857879
|
A | T | 1 | a0001c0001t0065g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.408+10846T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857879 | ||||||
| chr13:101857998
|
C | T | 101 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.408+10727G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101857998 | ||||||
| chr13:101858151
|
G | T | 1 | a0001c0001t0011g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.408+10574C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858151 | ||||||
| chr13:101858229
|
T | TA | 161 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.408+10495dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858229 | ||||||
| chr13:101858325
|
T | C | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+10400A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858325 | ||||||
| chr13:101858497
|
T | C | 1 | a0001c0001t0064g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.408+10228A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858497 | ||||||
| chr13:101858524
|
T | G | 146 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(143): Show | 146 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.408+10201A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858524 | ||||||
| chr13:101858770
|
G | C | 1 | a0001c0001t0033g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.408+9955C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858770 | ||||||
| chr13:101858804
|
A | G | 145 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.408+9921T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858804 | ||||||
| chr13:101858827
|
A | G | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+9898T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858827 | ||||||
| chr13:101858968
|
G | A | 1 | a0001c0002t0014g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.408+9757C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101858968 | ||||||
| chr13:101859005
|
T | C | 37 | a0001c0001t0003g0076a0001c0001t0003g0110a0001c0001t0008g0173others(34): Show | 37 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.408+9720A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859005 | ||||||
| chr13:101859068
|
T | A | 1 | a0001c0001t0114g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.408+9657A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859068 | ||||||
| chr13:101859118
|
C | T | 87 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(84): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.408+9607G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859118 | ||||||
| chr13:101859176
|
G | A | 98 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.408+9549C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859176 | ||||||
| chr13:101859460
|
G | A | 1 | a0001c0001t0122g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.408+9265C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859460 | ||||||
| chr13:101859484
|
A | G | 1 | a0001c0001t0015g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.408+9241T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859484 | ||||||
| chr13:101859964
|
T | A | 8 | a0001c0001t0017g0136a0001c0001t0079g0013a0001c0001t0102g0138others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+8761A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101859964 | ||||||
| chr13:101860063
|
G | A | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.408+8662C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860063 | ||||||
| chr13:101860158
|
C | T | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+8567G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860158 | ||||||
| chr13:101860190
|
C | G | 162 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.408+8535G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860190 | ||||||
| chr13:101860300
|
T | A | 96 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0065others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.408+8425A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860300 | ||||||
| chr13:101860521
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+8204A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860521 | ||||||
| chr13:101860588
|
A | T | 113 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0055others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.408+8137T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860588 | ||||||
| chr13:101860690
|
T | C | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+8035A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860690 | ||||||
| chr13:101860712
|
G | C | 1 | a0001c0001t0012g0191 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.408+8013C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860712 | ||||||
| chr13:101860756
|
T | A | 14 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+7969A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860756 | ||||||
| chr13:101860995
|
T | A | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.408+7730A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101860995 | ||||||
| chr13:101861015
|
T | C | 1 | a0001c0001t0123g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.408+7710A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861015 | ||||||
| chr13:101861188
|
T | G | 1 | a0001c0001t0154g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.408+7537A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861188 | ||||||
| chr13:101861431
|
G | C | 2 | a0001c0001t0023g0157a0001c0001t0023g0158 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.408+7294C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861431 | ||||||
| chr13:101861556
|
CA | C | 103 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0055others(100): Show | 103 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.408+7168delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861556 | ||||||
| chr13:101861603
|
T | C | 17 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.408+7122A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861603 | ||||||
| chr13:101861617
|
C | T | 1 | a0001c0002t0014g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.408+7108G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861617 | ||||||
| chr13:101861839
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0146g0156 | 2 | HG01884.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.408+6886G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861839 | ||||||
| chr13:101861908
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.408+6817T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861908 | ||||||
| chr13:101861919
|
G | T | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.408+6806C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101861919 | ||||||
| chr13:101862167
|
G | A | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+6558C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862167 | ||||||
| chr13:101862191
|
C | G | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.408+6534G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862191 | ||||||
| chr13:101862334
|
T | C | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.408+6391A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862334 | ||||||
| chr13:101862411
|
C | T | 49 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0065others(46): Show | 49 | HG00323.hp1 HG00621.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.408+6314G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862411 | ||||||
| chr13:101862548
|
G | A | 7 | a0001c0001t0016g0010a0001c0001t0029g0115a0001c0001t0045g0214others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+6177C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862548 | ||||||
| chr13:101862938
|
T | G | 1 | a0001c0001t0004g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.408+5787A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101862938 | ||||||
| chr13:101863473
|
A | G | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.408+5252T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863473 | ||||||
| chr13:101863680
|
A | G | 2 | a0001c0001t0107g0175a0001c0001t0145g0174 | 2 | HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.408+5045T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863680 | ||||||
| chr13:101863720
|
A | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+5005T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863720 | ||||||
| chr13:101863739
|
A | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+4986T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863739 | ||||||
| chr13:101863751
|
C | T | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.408+4974G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863751 | ||||||
| chr13:101863967
|
G | A | 71 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.408+4758C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101863967 | ||||||
| chr13:101864163
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.408+4562C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864163 | ||||||
| chr13:101864174
|
C | A | 2 | a0001c0001t0151g0147a0001c0002t0014g0118 | 2 | HG01192.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.408+4551G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864174 | ||||||
| chr13:101864197
|
T | C | 1 | a0001c0001t0087g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.408+4528A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864197 | ||||||
| chr13:101864443
|
T | C | 2 | a0001c0001t0023g0164a0001c0001t0148g0167 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.408+4282A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864443 | ||||||
| chr13:101864455
|
G | A | 1 | a0001c0001t0158g0264 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.408+4270C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864455 | ||||||
| chr13:101864521
|
A | G | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.408+4204T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864521 | ||||||
| chr13:101864581
|
C | T | 1 | a0001c0001t0046g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.408+4144G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864581 | ||||||
| chr13:101864967
|
G | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(144): Show | 147 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.408+3758C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101864967 | ||||||
| chr13:101865043
|
C | A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+3682G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865043 | ||||||
| chr13:101865130
|
T | C | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+3595A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865130 | ||||||
| chr13:101865208
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+3517A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865208 | ||||||
| chr13:101865234
|
G | A | 1 | a0001c0001t0064g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.408+3491C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865234 | ||||||
| chr13:101865454
|
C | T | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.408+3271G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865454 | ||||||
| chr13:101865481
|
G | T | 1 | a0001c0001t0002g0055 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.408+3244C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865481 | ||||||
| chr13:101865898
|
G | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(144): Show | 147 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.408+2827C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865898 | ||||||
| chr13:101865912
|
A | T | 29 | a0001c0001t0003g0106a0001c0001t0004g0088a0001c0001t0008g0208others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.408+2813T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101865912 | ||||||
| chr13:101866075
|
A | C | 1 | a0001c0001t0104g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.408+2650T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866075 | ||||||
| chr13:101866129
|
T | C | 149 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(146): Show | 149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.408+2596A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866129 | ||||||
| chr13:101866181
|
T | C | 4 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243others(1): Show | 4 | HG02970.hp2 HG03195.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+2544A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866181 | ||||||
| chr13:101866229
|
T | C | 1 | a0001c0001t0006g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.408+2496A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866229 | ||||||
| chr13:101866340
|
G | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(144): Show | 147 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.408+2385C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866340 | ||||||
| chr13:101866596
|
C | CTAT | 172 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(169): Show | 172 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.408+2126_408+2128d others(5): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101866596 | ||||||
| chr13:101867096
|
T | C | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.408+1629A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867096 | ||||||
| chr13:101867143
|
A | G | 156 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0132others(153): Show | 156 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.408+1582T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867143 | ||||||
| chr13:101867174
|
G | A | 1 | a0001c0001t0125g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.408+1551C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867174 | ||||||
| chr13:101867344
|
T | C | 2 | a0001c0001t0011g0223a0001c0001t0074g0122 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.408+1381A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867344 | ||||||
| chr13:101867668
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.408+1057G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867668 | ||||||
| chr13:101867875
|
A | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+850T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867875 | ||||||
| chr13:101867889
|
G | GAC | 54 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0127others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.408+834_408+835dup others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
G | GACAC | 18 | a0001c0001t0001g0075a0001c0001t0002g0101a0001c0001t0002g0109others(15): Show | 18 | HG00408.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+832_408+835dup others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
G | GACACAC | 6 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0005g0103others(3): Show | 6 | HG01074.hp1 HG01169.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+830_408+835dup others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GAC | G | 27 | a0001c0001t0002g0055a0001c0001t0006g0083a0001c0001t0008g0233others(24): Show | 27 | HG00408.hp2 HG01074.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.408+834_408+835del others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACAC | G | 37 | a0001c0001t0004g0088a0001c0001t0008g0208a0001c0001t0009g0179others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.408+832_408+835del others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACAC | G | 24 | a0001c0001t0001g0016a0001c0001t0003g0106a0001c0001t0008g0152others(21): Show | 24 | HG01106.hp2 HG01884.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.408+830_408+835del others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(1): Show |
G | 7 | a0001c0001t0021g0170a0001c0001t0021g0225a0001c0001t0051g0002others(4): Show | 7 | HG02015.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+828_408+835del others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(3): Show |
G | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.408+826_408+835del others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(5): Show |
G | 5 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+824_408+835del others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.408+822_408+835del others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(11): Show |
G | 1 | a0001c0001t0006g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.408+818_408+835del others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867889
|
GACACACA others(13): Show |
G | 1 | a0001c0001t0008g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.408+816_408+835del others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867889 | ||||||
| chr13:101867913
|
C | T | 1 | a0001c0001t0137g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.408+812G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867913 | ||||||
| chr13:101867918
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+789_408+806del others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867918 | ||||||
| chr13:101867926
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.408+789_408+798del others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867926 | ||||||
| chr13:101867928
|
ACACACAC others(1): Show |
A | 23 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0058others(20): Show | 23 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.408+789_408+796del others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867928 | ||||||
| chr13:101867930
|
ACACACG | A | 9 | a0001c0001t0012g0216a0001c0001t0017g0139a0001c0001t0028g0018others(6): Show | 9 | HG01891.hp1 HG02523.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+789_408+794del others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867930 | ||||||
| chr13:101867932
|
A | G | 5 | a0001c0001t0003g0106a0001c0001t0009g0203a0001c0001t0133g0211others(2): Show | 5 | HG00423.hp2 HG01496.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+793T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867932 | ||||||
| chr13:101867932
|
ACACG | A | 5 | a0001c0001t0016g0130a0001c0001t0036g0061a0001c0001t0036g0062others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+789_408+792del others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867932 | ||||||
| chr13:101867934
|
A | G | 46 | a0001c0001t0003g0106a0001c0001t0004g0088a0001c0001t0006g0085others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.408+791T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867934 | ||||||
| chr13:101867934
|
ACG | A | 3 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0083g0131 | 3 | HG02257.hp2 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.408+789_408+790del others(2): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867934 | ||||||
| chr13:101867936
|
G | A | 6 | a0001c0001t0016g0012a0001c0001t0026g0123a0001c0001t0046g0148others(3): Show | 6 | HG01074.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+789C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867936 | ||||||
| chr13:101867938
|
G | A | 1 | a0001c0001t0100g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.408+787C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101867938 | ||||||
| chr13:101868177
|
G | A | 1 | a0001c0001t0152g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.408+548C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868177 | ||||||
| chr13:101868186
|
G | A | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.408+539C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868186 | ||||||
| chr13:101868411
|
C | A | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+314G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868411 | ||||||
| chr13:101868424
|
T | G | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.408+301A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868424 | ||||||
| chr13:101868495
|
A | T | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+230T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868495 | ||||||
| chr13:101868534
|
C | T | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.408+191G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 3/4 | chr13 | 101868534 | ||||||
| chr13:101869069
|
T | C | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.305-241A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869069 | ||||||
| chr13:101869243
|
G | A | 1 | a0001c0001t0154g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.305-415C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869243 | ||||||
| chr13:101869309
|
C | T | 46 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0065others(43): Show | 46 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.305-481G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869309 | ||||||
| chr13:101869315
|
C | T | 44 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0002g0065others(41): Show | 44 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.305-487G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869315 | ||||||
| chr13:101869337
|
C | G | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.305-509G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869337 | ||||||
| chr13:101869495
|
A | G | 1 | a0001c0001t0121g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.305-667T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869495 | ||||||
| chr13:101869545
|
T | C | 1 | a0001c0001t0080g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.305-717A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869545 | ||||||
| chr13:101869968
|
G | A | 4 | a0001c0001t0090g0015a0001c0001t0098g0014a0001c0001t0106g0163others(1): Show | 4 | HG02572.hp1 HG02622.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-1140C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101869968 | ||||||
| chr13:101870284
|
C | G | 1 | a0001c0002t0014g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.305-1456G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870284 | ||||||
| chr13:101870413
|
T | C | 3 | a0001c0001t0090g0015a0001c0001t0106g0163a0001c0001t0130g0219 | 3 | HG02572.hp1 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.305-1585A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870413 | ||||||
| chr13:101870691
|
G | A | 2 | a0001c0001t0015g0124a0001c0002t0014g0118 | 2 | HG01192.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.305-1863C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870691 | ||||||
| chr13:101870817
|
G | A | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.305-1989C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870817 | ||||||
| chr13:101870975
|
A | AATAC | 15 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0017g0136others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.305-2151_305-2148d others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870975 | ||||||
| chr13:101870975
|
A | AATACATA others(1): Show |
31 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0058others(28): Show | 31 | HG00438.hp2 HG00621.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.305-2155_305-2148d others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870975 | ||||||
| chr13:101870975
|
A | AATACATA others(5): Show |
1 | a0001c0001t0006g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.305-2159_305-2148d others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870975 | ||||||
| chr13:101870975
|
A | C | 8 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(5): Show | 8 | HG01109.hp2 HG01192.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2147T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870975 | ||||||
| chr13:101870985
|
T | C | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.305-2157A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101870985 | ||||||
| chr13:101871103
|
G | A | 1 | a0001c0001t0101g0105 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.305-2275C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101871103 | ||||||
| chr13:101871181
|
T | C | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.305-2353A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101871181 | ||||||
| chr13:101871546
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.305-2718A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101871546 | ||||||
| chr13:101871620
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.305-2792A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101871620 | ||||||
| chr13:101871891
|
A | G | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.305-3063T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101871891 | ||||||
| chr13:101872086
|
T | A | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.304+3100A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872086 | ||||||
| chr13:101872100
|
T | G | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.304+3086A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872100 | ||||||
| chr13:101872232
|
T | C | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.304+2954A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872232 | ||||||
| chr13:101872258
|
G | T | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.304+2928C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872258 | ||||||
| chr13:101872314
|
G | C | 1 | a0001c0001t0067g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.304+2872C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872314 | ||||||
| chr13:101872364
|
A | G | 5 | a0001c0001t0013g0212a0001c0001t0017g0136a0001c0001t0079g0013others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+2822T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872364 | ||||||
| chr13:101872446
|
A | G | 1 | a0001c0001t0009g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.304+2740T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872446 | ||||||
| chr13:101872665
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304+2521G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872665 | ||||||
| chr13:101872824
|
G | A | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.304+2362C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101872824 | ||||||
| chr13:101873029
|
G | GA | 39 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0058others(36): Show | 39 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.304+2156dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873029 | ||||||
| chr13:101873029
|
GA | G | 31 | a0001c0001t0001g0132a0001c0001t0013g0142a0001c0001t0013g0143others(28): Show | 31 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.304+2156delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873029 | ||||||
| chr13:101873041
|
A | C | 18 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+2145T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873041 | ||||||
| chr13:101873439
|
T | C | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304+1747A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873439 | ||||||
| chr13:101873571
|
C | G | 6 | a0001c0001t0001g0033a0001c0001t0005g0067a0001c0001t0010g0201others(3): Show | 6 | HG02015.hp1 HG02559.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1615G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873571 | ||||||
| chr13:101873572
|
G | C | 18 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+1614C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873572 | ||||||
| chr13:101873716
|
T | C | 1 | a0001c0001t0018g0221 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.304+1470A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873716 | ||||||
| chr13:101873784
|
C | A | 18 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+1402G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873784 | ||||||
| chr13:101873897
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+1289T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873897 | ||||||
| chr13:101873962
|
A | G | 2 | a0001c0001t0036g0061a0001c0001t0036g0062 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.304+1224T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101873962 | ||||||
| chr13:101874145
|
T | A | 1 | a0001c0001t0125g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.304+1041A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101874145 | ||||||
| chr13:101874687
|
T | C | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.304+499A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101874687 | ||||||
| chr13:101874806
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.304+380C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 2/4 | chr13 | 101874806 | ||||||
| chr13:101875503
|
C | G | 3 | a0001c0001t0040g0188a0001c0001t0040g0189a0001c0001t0109g0199 | 3 | NA18948.hp1 NA18964.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.194-207G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101875503 | ||||||
| chr13:101875706
|
T | C | 1 | a0001c0001t0053g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.194-410A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101875706 | ||||||
| chr13:101875728
|
T | A | 15 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.194-432A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101875728 | ||||||
| chr13:101875905
|
G | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-609C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101875905 | ||||||
| chr13:101876187
|
T | C | 21 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.194-891A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876187 | ||||||
| chr13:101876268
|
G | A | 1 | a0001c0001t0024g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.194-972C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876268 | ||||||
| chr13:101876282
|
C | T | 17 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-986G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876282 | ||||||
| chr13:101876338
|
G | A | 1 | a0001c0001t0157g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.194-1042C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876338 | ||||||
| chr13:101876357
|
G | A | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-1061C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876357 | ||||||
| chr13:101876370
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.194-1074C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876370 | ||||||
| chr13:101876524
|
C | T | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.194-1228G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876524 | ||||||
| chr13:101876584
|
T | C | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194-1288A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876584 | ||||||
| chr13:101876736
|
T | C | 1 | a0001c0001t0038g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.194-1440A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876736 | ||||||
| chr13:101876762
|
C | T | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-1466G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876762 | ||||||
| chr13:101876799
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.194-1503C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876799 | ||||||
| chr13:101876985
|
T | C | 110 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(107): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.194-1689A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101876985 | ||||||
| chr13:101877162
|
G | A | 108 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(105): Show | 108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.194-1866C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877162 | ||||||
| chr13:101877579
|
C | A | 18 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0019g0227others(15): Show | 18 | HG01993.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.194-2283G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877579 | ||||||
| chr13:101877639
|
C | G | 110 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(107): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.194-2343G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877639 | ||||||
| chr13:101877855
|
T | G | 1 | a0001c0001t0003g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.194-2559A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877855 | ||||||
| chr13:101877870
|
A | G | 2 | a0001c0001t0029g0115a0001c0002t0014g0118 | 2 | HG01192.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.194-2574T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877870 | ||||||
| chr13:101877900
|
C | A | 2 | a0001c0001t0036g0061a0001c0001t0036g0062 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.194-2604G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101877900 | ||||||
| chr13:101878076
|
C | T | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194-2780G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878076 | ||||||
| chr13:101878452
|
A | G | 9 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-3156T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878452 | ||||||
| chr13:101878555
|
T | G | 9 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-3259A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878555 | ||||||
| chr13:101878560
|
C | A | 1 | a0001c0001t0151g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.194-3264G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878560 | ||||||
| chr13:101878580
|
A | T | 3 | a0001c0001t0005g0103a0001c0001t0033g0095a0001c0001t0069g0024 | 3 | HG02071.hp2 NA18992.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.194-3284T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878580 | ||||||
| chr13:101878582
|
A | T | 3 | a0001c0001t0005g0103a0001c0001t0033g0095a0001c0001t0069g0024 | 3 | HG02071.hp2 NA18992.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.194-3286T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878582 | ||||||
| chr13:101878684
|
A | C | 2 | a0001c0001t0021g0170a0001c0001t0110g0182 | 2 | HG02970.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.194-3388T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878684 | ||||||
| chr13:101878877
|
AT | A | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.194-3582delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878877 | ||||||
| chr13:101878880
|
T | A | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.194-3584A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878880 | ||||||
| chr13:101878942
|
T | C | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(112): Show | 115 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.194-3646A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878942 | ||||||
| chr13:101878949
|
T | TACAAGA | 243 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(240): Show | 243 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.194-3654_194-3653i others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878949 | ||||||
| chr13:101878964
|
T | A | 4 | a0001c0001t0050g0001a0001c0001t0051g0002a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-3668A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101878964 | ||||||
| chr13:101879068
|
A | G | 1 | a0001c0001t0099g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.194-3772T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879068 | ||||||
| chr13:101879391
|
C | T | 1 | a0001c0002t0127g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.194-4095G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879391 | ||||||
| chr13:101879412
|
A | G | 17 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-4116T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879412 | ||||||
| chr13:101879491
|
T | C | 1 | a0001c0001t0019g0227 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.194-4195A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879491 | ||||||
| chr13:101879580
|
C | A | 4 | a0001c0001t0009g0255a0001c0001t0034g0038a0001c0001t0037g0087others(1): Show | 4 | HG00642.hp1 HG01074.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-4284G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879580 | ||||||
| chr13:101879613
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.194-4317A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879613 | ||||||
| chr13:101879743
|
T | C | 2 | a0001c0001t0003g0076a0001c0001t0072g0077 | 2 | HG01934.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.194-4447A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879743 | ||||||
| chr13:101879754
|
G | GA | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(112): Show | 115 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.194-4459dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879754 | ||||||
| chr13:101879773
|
A | G | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.194-4477T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879773 | ||||||
| chr13:101879777
|
G | A | 1 | a0001c0001t0057g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-4481C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879777 | ||||||
| chr13:101879823
|
G | A | 1 | a0001c0001t0019g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.194-4527C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101879823 | ||||||
| chr13:101880192
|
T | C | 101 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(98): Show | 101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.194-4896A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880192 | ||||||
| chr13:101880229
|
T | C | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.194-4933A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880229 | ||||||
| chr13:101880270
|
G | C | 17 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-4974C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880270 | ||||||
| chr13:101880305
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194-5009G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880305 | ||||||
| chr13:101880483
|
C | G | 1 | a0001c0001t0145g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.194-5187G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880483 | ||||||
| chr13:101880539
|
T | C | 101 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(98): Show | 101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.194-5243A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880539 | ||||||
| chr13:101880543
|
C | T | 41 | a0001c0001t0003g0106a0001c0001t0004g0088a0001c0001t0008g0208others(38): Show | 41 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.194-5247G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880543 | ||||||
| chr13:101880754
|
T | C | 4 | a0001c0001t0024g0261a0001c0001t0131g0162a0001c0001t0160g0258others(1): Show | 4 | HG02145.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-5458A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880754 | ||||||
| chr13:101880816
|
T | C | 1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194-5520A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880816 | ||||||
| chr13:101880834
|
C | T | 12 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0017g0139others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-5538G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101880834 | ||||||
| chr13:101881048
|
C | T | 80 | a0001c0001t0003g0076a0001c0001t0003g0106a0001c0001t0003g0110others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.194-5752G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101881048 | ||||||
| chr13:101881383
|
T | A | 27 | a0001c0001t0003g0106a0001c0001t0004g0088a0001c0001t0008g0208others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.194-6087A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101881383 | ||||||
| chr13:101881560
|
T | C | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-6264A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101881560 | ||||||
| chr13:101881592
|
C | T | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-6296G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101881592 | ||||||
| chr13:101881635
|
AC | A | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-6340delG | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101881635 | ||||||
| chr13:101882070
|
C | CT | 4 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0021g0170others(1): Show | 4 | HG01106.hp2 HG01433.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-6775dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882070 | ||||||
| chr13:101882144
|
C | A | 220 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0036others(217): Show | 220 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.194-6848G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882144 | ||||||
| chr13:101882216
|
G | A | 1 | a0001c0001t0046g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.194-6920C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882216 | ||||||
| chr13:101882333
|
T | C | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.194-7037A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882333 | ||||||
| chr13:101882428
|
C | T | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.194-7132G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882428 | ||||||
| chr13:101882550
|
G | GT | 6 | a0001c0001t0017g0136a0001c0001t0068g0009a0001c0001t0079g0013others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-7255dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882550 | ||||||
| chr13:101882550
|
GT | G | 91 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(88): Show | 91 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.194-7255delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882550 | ||||||
| chr13:101882552
|
T | G | 2 | a0001c0001t0001g0036a0001c0001t0031g0035 | 2 | HG01168.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.194-7256A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882552 | ||||||
| chr13:101882590
|
T | A | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-7294A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882590 | ||||||
| chr13:101882774
|
C | T | 93 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(90): Show | 93 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.194-7478G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882774 | ||||||
| chr13:101882842
|
A | G | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-7546T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101882842 | ||||||
| chr13:101883006
|
G | C | 70 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.194-7710C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883006 | ||||||
| chr13:101883013
|
G | A | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.194-7717C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883013 | ||||||
| chr13:101883239
|
G | C | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-7943C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883239 | ||||||
| chr13:101883277
|
G | A | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.194-7981C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883277 | ||||||
| chr13:101883280
|
G | A | 78 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.194-7984C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883280 | ||||||
| chr13:101883325
|
T | C | 20 | a0001c0001t0003g0106a0001c0001t0004g0088a0001c0001t0008g0208others(17): Show | 20 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.194-8029A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883325 | ||||||
| chr13:101883356
|
A | C | 1 | a0001c0001t0034g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.194-8060T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883356 | ||||||
| chr13:101883458
|
C | T | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-8162G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883458 | ||||||
| chr13:101883481
|
C | T | 1 | a0001c0001t0081g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.194-8185G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883481 | ||||||
| chr13:101883515
|
A | C | 98 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(95): Show | 98 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.194-8219T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883515 | ||||||
| chr13:101883679
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.194-8383C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883679 | ||||||
| chr13:101883695
|
C | T | 94 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.194-8399G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883695 | ||||||
| chr13:101883706
|
T | G | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.194-8410A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883706 | ||||||
| chr13:101883757
|
C | T | 2 | a0001c0001t0160g0258a0001c0001t0161g0263 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.194-8461G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883757 | ||||||
| chr13:101883803
|
C | T | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-8507G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883803 | ||||||
| chr13:101883907
|
G | A | 16 | a0001c0001t0001g0132a0001c0001t0013g0212a0001c0001t0016g0012others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-8611C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883907 | ||||||
| chr13:101883941
|
TA | T | 34 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0058others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.194-8646delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101883941 | ||||||
| chr13:101884015
|
A | G | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-8719T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884015 | ||||||
| chr13:101884017
|
C | T | 95 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(92): Show | 95 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.194-8721G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884017 | ||||||
| chr13:101884019
|
C | T | 3 | a0001c0001t0091g0117a0001c0001t0094g0119a0001c0002t0014g0116 | 3 | HG02965.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.194-8723G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884019 | ||||||
| chr13:101884062
|
C | CA | 35 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0001t0003g0058others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.194-8767dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0010g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.194-8776_194-8767d others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0024g0260a0001c0001t0124g0251a0001c0002t0014g0116 | 3 | HG02647.hp2 HG02965.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.194-8779_194-8767d others(15): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(7): Show |
24 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0093others(21): Show | 24 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.194-8780_194-8767d others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(8): Show |
30 | a0001c0001t0002g0096a0001c0001t0002g0098a0001c0001t0002g0104others(27): Show | 30 | HG00621.hp2 HG01081.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.194-8781_194-8767d others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(9): Show |
12 | a0001c0001t0001g0029a0001c0001t0011g0235a0001c0001t0015g0114others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-8782_194-8767d others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0005g0103a0001c0001t0013g0142a0001c0001t0013g0143others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-8783_194-8767d others(19): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0109 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.194-8787_194-8767d others(23): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
CA | C | 89 | a0001c0001t0003g0076a0001c0001t0003g0106a0001c0001t0003g0110others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.194-8767delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884062
|
CAAA | C | 17 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0009g0241others(14): Show | 17 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-8769_194-8767d others(5): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884062 | ||||||
| chr13:101884157
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0009g0159a0001c0001t0009g0241others(15): Show | 18 | HG01884.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.194-8861C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884157 | ||||||
| chr13:101884177
|
G | A | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.194-8881C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884177 | ||||||
| chr13:101884287
|
T | C | 95 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(92): Show | 95 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.194-8991A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884287 | ||||||
| chr13:101884393
|
A | G | 79 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.194-9097T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884393 | ||||||
| chr13:101884416
|
G | A | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.194-9120C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884416 | ||||||
| chr13:101884631
|
T | C | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.194-9335A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884631 | ||||||
| chr13:101884778
|
G | A | 93 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(90): Show | 93 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.194-9482C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884778 | ||||||
| chr13:101884860
|
CACAT | C | 7 | a0001c0001t0018g0236a0001c0001t0029g0115a0001c0001t0091g0117others(4): Show | 7 | HG01192.hp2 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-9568_194-9565d others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884860 | ||||||
| chr13:101884864
|
TACATAC | T | 86 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0075others(83): Show | 86 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-9574_194-9569d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884864 | ||||||
| chr13:101884868
|
T | C | 1 | a0001c0001t0008g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.194-9572A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884868 | ||||||
| chr13:101884868
|
T | TAC | 13 | a0001c0001t0006g0059a0001c0001t0017g0136a0001c0001t0030g0023others(10): Show | 13 | HG01978.hp2 HG02109.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.194-9574_194-9573d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884868 | ||||||
| chr13:101884874
|
C | T | 1 | a0001c0001t0018g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.194-9578G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884874 | ||||||
| chr13:101884916
|
C | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.194-9620G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101884916 | ||||||
| chr13:101885175
|
T | C | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-9879A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885175 | ||||||
| chr13:101885372
|
A | C | 2 | a0001c0001t0045g0214a0001c0001t0045g0215 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194-10076T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885372 | ||||||
| chr13:101885668
|
T | C | 154 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0075others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.194-10372A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885668 | ||||||
| chr13:101885701
|
G | GA | 23 | a0001c0001t0001g0029a0001c0001t0006g0073a0001c0001t0009g0159others(20): Show | 23 | HG01192.hp1 HG01884.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.194-10406dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885701 | ||||||
| chr13:101885701
|
GA | G | 21 | a0001c0001t0001g0016a0001c0001t0004g0057a0001c0001t0004g0070others(18): Show | 21 | HG01496.hp1 HG01891.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.194-10406delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885701 | ||||||
| chr13:101885739
|
T | C | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-10443A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885739 | ||||||
| chr13:101885762
|
C | A | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-10466G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885762 | ||||||
| chr13:101885781
|
G | A | 1 | a0001c0001t0026g0027 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.194-10485C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885781 | ||||||
| chr13:101885819
|
G | A | 131 | a0001c0001t0001g0016a0001c0001t0003g0106a0001c0001t0005g0067others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.194-10523C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885819 | ||||||
| chr13:101885839
|
G | T | 1 | a0001c0001t0049g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.194-10543C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885839 | ||||||
| chr13:101885844
|
T | G | 131 | a0001c0001t0001g0016a0001c0001t0003g0106a0001c0001t0005g0067others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.194-10548A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885844 | ||||||
| chr13:101885947
|
G | T | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.194-10651C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885947 | ||||||
| chr13:101885952
|
C | T | 135 | a0001c0001t0001g0016a0001c0001t0003g0106a0001c0001t0005g0067others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.194-10656G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101885952 | ||||||
| chr13:101886034
|
A | C | 1 | a0001c0001t0009g0255 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.194-10738T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886034 | ||||||
| chr13:101886190
|
G | C | 2 | a0001c0001t0045g0214a0001c0001t0045g0215 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194-10894C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886190 | ||||||
| chr13:101886195
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-10899G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886195 | ||||||
| chr13:101886242
|
C | T | 4 | a0001c0001t0017g0139a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-10946G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886242 | ||||||
| chr13:101886349
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.194-11053C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886349 | ||||||
| chr13:101886360
|
C | T | 119 | a0001c0001t0003g0106a0001c0001t0005g0067a0001c0001t0008g0151others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.194-11064G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886360 | ||||||
| chr13:101886369
|
G | C | 2 | a0001c0001t0016g0010a0001c0001t0099g0011 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.194-11073C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886369 | ||||||
| chr13:101886552
|
A | C | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.194-11256T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886552 | ||||||
| chr13:101886599
|
G | A | 101 | a0001c0001t0003g0106a0001c0001t0005g0067a0001c0001t0008g0173others(98): Show | 101 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.194-11303C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886599 | ||||||
| chr13:101886827
|
A | G | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.194-11531T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886827 | ||||||
| chr13:101886984
|
C | T | 2 | a0001c0001t0020g0250a0001c0001t0052g0003 | 2 | HG00438.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.194-11688G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101886984 | ||||||
| chr13:101887322
|
A | ATG | 84 | a0001c0001t0003g0106a0001c0001t0008g0173a0001c0001t0008g0208others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.194-12028_194-1202 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887322 | ||||||
| chr13:101887328
|
G | GTGTA | 22 | a0001c0001t0008g0151a0001c0001t0011g0235a0001c0001t0012g0230others(19): Show | 22 | HG00280.hp1 HG01175.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-12033_194-1203 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887328 | ||||||
| chr13:101887330
|
A | G | 10 | a0001c0001t0011g0190a0001c0001t0017g0139a0001c0001t0045g0214others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-12034T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887330 | ||||||
| chr13:101887338
|
A | G | 2 | a0001c0001t0032g0039a0001c0001t0084g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.194-12042T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887338 | ||||||
| chr13:101887345
|
T | C | 4 | a0001c0001t0015g0114a0001c0001t0066g0112a0001c0001t0081g0120others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-12049A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887345 | ||||||
| chr13:101887347
|
C | T | 107 | a0001c0001t0003g0106a0001c0001t0008g0151a0001c0001t0008g0152others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.194-12051G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887347 | ||||||
| chr13:101887349
|
C | T | 5 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0150g0146others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-12053G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887349 | ||||||
| chr13:101887579
|
T | C | 1 | a0001c0001t0034g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.194-12283A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887579 | ||||||
| chr13:101887591
|
G | T | 96 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.194-12295C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887591 | ||||||
| chr13:101887602
|
TGAA | T | 3 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243 | 3 | HG02970.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.194-12309_194-1230 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887602 | ||||||
| chr13:101887768
|
G | A | 1 | a0001c0001t0054g0004 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.194-12472C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887768 | ||||||
| chr13:101887846
|
C | T | 114 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0008g0173others(111): Show | 114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.194-12550G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887846 | ||||||
| chr13:101887873
|
A | G | 1 | a0001c0001t0074g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.194-12577T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101887873 | ||||||
| chr13:101888108
|
T | C | 103 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.194-12812A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888108 | ||||||
| chr13:101888300
|
ATGATTGG others(10): Show |
A | 4 | a0001c0001t0017g0139a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13021_194-1300 others(21): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888300 | ||||||
| chr13:101888320
|
TAAAA | T | 4 | a0001c0001t0017g0139a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13028_194-1302 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888320 | ||||||
| chr13:101888415
|
T | C | 1 | a0001c0001t0018g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.194-13119A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888415 | ||||||
| chr13:101888529
|
A | G | 1 | a0001c0001t0068g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.194-13233T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888529 | ||||||
| chr13:101888555
|
T | G | 265 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.194-13259A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888555 | ||||||
| chr13:101888599
|
TTATGATG others(5): Show |
T | 4 | a0001c0001t0018g0221a0001c0001t0020g0217a0001c0001t0117g0229others(1): Show | 4 | HG00408.hp2 NA18969.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13315_194-1330 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888599 | ||||||
| chr13:101888739
|
G | A | 2 | a0001c0001t0130g0219a0001c0001t0147g0220 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.194-13443C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888739 | ||||||
| chr13:101888772
|
A | G | 4 | a0001c0001t0045g0214a0001c0001t0045g0215a0001c0001t0047g0213others(1): Show | 4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13476T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888772 | ||||||
| chr13:101888842
|
AG | A | 79 | a0001c0001t0001g0033a0001c0001t0001g0075a0001c0001t0001g0127others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.194-13547delC | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888842 | ||||||
| chr13:101888955
|
G | A | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-13659C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101888955 | ||||||
| chr13:101889186
|
A | G | 125 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(122): Show | 125 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.194-13890T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889186 | ||||||
| chr13:101889203
|
T | A | 2 | a0001c0001t0050g0001a0001c0001t0051g0002 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.194-13907A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889203 | ||||||
| chr13:101889233
|
A | AT | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-13938dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889233 | ||||||
| chr13:101889287
|
C | G | 131 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.194-13991G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889287 | ||||||
| chr13:101889315
|
C | T | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.194-14019G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889315 | ||||||
| chr13:101889344
|
G | A | 125 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(122): Show | 125 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.194-14048C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889344 | ||||||
| chr13:101889621
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0090g0015a0001c0001t0098g0014 | 3 | HG01993.hp1 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.194-14325C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889621 | ||||||
| chr13:101889686
|
A | G | 1 | a0001c0001t0029g0115 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194-14390T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101889686 | ||||||
| chr13:101890014
|
T | C | 2 | a0001c0001t0002g0065a0001c0001t0067g0091 | 2 | HG00621.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.194-14718A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890014 | ||||||
| chr13:101890124
|
C | T | 1 | a0001c0001t0044g0178 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.194-14828G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890124 | ||||||
| chr13:101890132
|
T | G | 1 | a0001c0001t0100g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.194-14836A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890132 | ||||||
| chr13:101890434
|
C | G | 3 | a0001c0001t0150g0146a0001c0001t0151g0147a0001c0001t0154g0145 | 3 | HG02109.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.194-15138G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890434 | ||||||
| chr13:101890653
|
A | G | 136 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.194-15357T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890653 | ||||||
| chr13:101890674
|
G | A | 1 | a0001c0001t0011g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.194-15378C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890674 | ||||||
| chr13:101890764
|
G | A | 129 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(126): Show | 129 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.194-15468C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890764 | ||||||
| chr13:101890765
|
T | A | 6 | a0001c0001t0028g0018a0001c0001t0028g0019a0001c0001t0080g0021others(3): Show | 6 | HG01891.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-15469A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890765 | ||||||
| chr13:101890923
|
G | A | 3 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0110g0182 | 3 | HG01106.hp2 HG01433.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.194-15627C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890923 | ||||||
| chr13:101890975
|
T | A | 4 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-15679A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101890975 | ||||||
| chr13:101891002
|
G | A | 2 | a0001c0001t0011g0235a0001c0001t0015g0124 | 2 | HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.194-15706C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891002 | ||||||
| chr13:101891038
|
C | G | 6 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-15742G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891038 | ||||||
| chr13:101891038
|
C | T | 128 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(125): Show | 128 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.194-15742G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891038 | ||||||
| chr13:101891055
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-15759T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891055 | ||||||
| chr13:101891197
|
T | C | 6 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-15901A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891197 | ||||||
| chr13:101891273
|
C | T | 1 | a0001c0002t0014g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-15977G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891273 | ||||||
| chr13:101891299
|
G | A | 2 | a0001c0001t0032g0039a0001c0001t0084g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.194-16003C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891299 | ||||||
| chr13:101891391
|
A | G | 5 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-16095T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891391 | ||||||
| chr13:101891483
|
T | C | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-16187A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891483 | ||||||
| chr13:101891915
|
A | G | 27 | a0001c0001t0008g0208a0001c0001t0009g0179a0001c0001t0009g0203others(24): Show | 27 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.194-16619T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101891915 | ||||||
| chr13:101892001
|
A | T | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-16705T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892001 | ||||||
| chr13:101892134
|
T | C | 1 | a0001c0001t0046g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.194-16838A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892134 | ||||||
| chr13:101892183
|
T | A | 4 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-16887A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892183 | ||||||
| chr13:101892289
|
G | T | 1 | a0001c0001t0120g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.194-16993C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892289 | ||||||
| chr13:101892329
|
A | G | 113 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.194-17033T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892329 | ||||||
| chr13:101892330
|
C | CA | 4 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-17035dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892330 | ||||||
| chr13:101892599
|
G | A | 120 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(117): Show | 120 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.194-17303C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892599 | ||||||
| chr13:101892621
|
A | G | 2 | a0001c0001t0102g0138a0001c0001t0104g0137 | 2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.194-17325T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892621 | ||||||
| chr13:101892637
|
C | A | 1 | a0001c0001t0042g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.194-17341G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892637 | ||||||
| chr13:101892886
|
C | T | 1 | a0001c0001t0059g0034 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.194-17590G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892886 | ||||||
| chr13:101892903
|
TGTTA | T | 6 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-17611_194-1760 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101892903 | ||||||
| chr13:101893057
|
C | T | 5 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-17761G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893057 | ||||||
| chr13:101893070
|
G | C | 3 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243 | 3 | HG02970.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.194-17774C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893070 | ||||||
| chr13:101893170
|
G | A | 113 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.194-17874C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893170 | ||||||
| chr13:101893235
|
G | A | 1 | a0001c0001t0067g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.194-17939C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893235 | ||||||
| chr13:101893335
|
G | A | 1 | a0001c0001t0073g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.194-18039C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893335 | ||||||
| chr13:101893627
|
T | C | 1 | a0001c0002t0014g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.194-18331A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893627 | ||||||
| chr13:101893637
|
T | C | 2 | a0001c0001t0016g0010a0001c0001t0099g0011 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.194-18341A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893637 | ||||||
| chr13:101893728
|
C | G | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-18432G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893728 | ||||||
| chr13:101893734
|
C | T | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.194-18438G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893734 | ||||||
| chr13:101893778
|
C | T | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-18482G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893778 | ||||||
| chr13:101893812
|
A | G | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-18516T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893812 | ||||||
| chr13:101893894
|
A | T | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-18598T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893894 | ||||||
| chr13:101893924
|
C | A | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-18628G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893924 | ||||||
| chr13:101893944
|
A | G | 1 | a0001c0001t0048g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-18648T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101893944 | ||||||
| chr13:101894023
|
C | CT | 10 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(7): Show | 10 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-18728dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894023 | ||||||
| chr13:101894023
|
CT | C | 127 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(124): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.194-18728delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894023 | ||||||
| chr13:101894189
|
G | GGATTGTA others(37): Show |
1 | a0001c0001t0007g0042 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.194-18937_194-1889 others(48): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894189 | ||||||
| chr13:101894229
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0038g0125a0001c0001t0064g0126others(1): Show | 4 | HG01175.hp1 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-18933T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894229 | ||||||
| chr13:101894299
|
C | T | 4 | a0001c0001t0023g0157a0001c0001t0023g0158a0001c0001t0146g0156others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-19003G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894299 | ||||||
| chr13:101894408
|
T | G | 3 | a0001c0001t0045g0214a0001c0001t0045g0215a0001c0001t0047g0213 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194-19112A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894408 | ||||||
| chr13:101894436
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.194-19140A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894436 | ||||||
| chr13:101894459
|
G | A | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-19163C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894459 | ||||||
| chr13:101894796
|
T | G | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.194-19500A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894796 | ||||||
| chr13:101894889
|
T | C | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-19593A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894889 | ||||||
| chr13:101894950
|
G | A | 3 | a0001c0001t0011g0235a0001c0001t0015g0124a0001c0001t0093g0111 | 3 | HG01175.hp2 HG03195.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.194-19654C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101894950 | ||||||
| chr13:101895136
|
T | C | 232 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0075others(229): Show | 232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.194-19840A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101895136 | ||||||
| chr13:101895625
|
G | C | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-20329C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101895625 | ||||||
| chr13:101895628
|
G | A | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-20332C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101895628 | ||||||
| chr13:101895743
|
A | G | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.194-20447T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101895743 | ||||||
| chr13:101896051
|
G | A | 1 | a0001c0001t0095g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193+20402C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896051 | ||||||
| chr13:101896153
|
CTTTTTAC others(37): Show |
C | 1 | a0001c0001t0007g0042 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.193+20256_193+2029 others(48): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896153 | ||||||
| chr13:101896334
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.193+20119A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896334 | ||||||
| chr13:101896338
|
G | A | 130 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(127): Show | 130 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.193+20115C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896338 | ||||||
| chr13:101896363
|
C | T | 2 | a0001c0001t0016g0012a0001c0001t0093g0111 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.193+20090G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896363 | ||||||
| chr13:101896375
|
C | T | 3 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153 | 3 | HG01081.hp1 HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.193+20078G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896375 | ||||||
| chr13:101896376
|
C | A | 2 | a0001c0001t0093g0111a0001c0001t0162g0265 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.193+20077G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896376 | ||||||
| chr13:101896386
|
A | G | 1 | a0001c0001t0110g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.193+20067T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896386 | ||||||
| chr13:101896396
|
T | G | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+20057A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896396 | ||||||
| chr13:101896471
|
T | C | 1 | a0001c0001t0017g0135 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+19982A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896471 | ||||||
| chr13:101896511
|
A | G | 27 | a0001c0001t0008g0208a0001c0001t0009g0179a0001c0001t0009g0203others(24): Show | 27 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.193+19942T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896511 | ||||||
| chr13:101896644
|
T | G | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+19809A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896644 | ||||||
| chr13:101896693
|
A | G | 6 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+19760T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896693 | ||||||
| chr13:101896708
|
T | C | 130 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(127): Show | 130 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.193+19745A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896708 | ||||||
| chr13:101896991
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+19462C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101896991 | ||||||
| chr13:101897322
|
C | T | 1 | a0001c0001t0032g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.193+19131G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897322 | ||||||
| chr13:101897418
|
A | G | 116 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0008g0173others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.193+19035T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897418 | ||||||
| chr13:101897467
|
C | T | 2 | a0001c0001t0016g0012a0001c0001t0093g0111 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.193+18986G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897467 | ||||||
| chr13:101897618
|
T | C | 1 | a0001c0001t0075g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.193+18835A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897618 | ||||||
| chr13:101897688
|
C | A | 1 | a0001c0001t0051g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+18765G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897688 | ||||||
| chr13:101897858
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0016g0012a0001c0001t0016g0130others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+18595A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897858 | ||||||
| chr13:101897948
|
G | A | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+18505C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897948 | ||||||
| chr13:101897961
|
C | T | 3 | a0001c0001t0012g0216a0001c0001t0021g0225a0001c0001t0042g0205 | 3 | HG02015.hp2 HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.193+18492G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897961 | ||||||
| chr13:101897988
|
G | A | 19 | a0001c0001t0009g0179a0001c0001t0009g0203a0001c0001t0010g0201others(16): Show | 19 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.193+18465C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101897988 | ||||||
| chr13:101898026
|
C | CT | 131 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.193+18426dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898026 | ||||||
| chr13:101898058
|
A | C | 138 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.193+18395T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898058 | ||||||
| chr13:101898115
|
G | C | 1 | a0001c0001t0156g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193+18338C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898115 | ||||||
| chr13:101898135
|
T | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+18318A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898135 | ||||||
| chr13:101898341
|
A | AAC | 26 | a0001c0001t0001g0033a0001c0001t0002g0104a0001c0001t0003g0058others(23): Show | 26 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.193+18110_193+1811 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACAC | 54 | a0001c0001t0001g0127a0001c0001t0002g0055a0001c0001t0002g0065others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.193+18108_193+1811 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACAC | 78 | a0001c0001t0001g0075a0001c0001t0004g0088a0001c0001t0006g0059others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.193+18106_193+1811 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(1): Show |
23 | a0001c0001t0010g0249a0001c0001t0012g0237a0001c0001t0016g0010others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+18104_193+1811 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(3): Show |
14 | a0001c0001t0008g0233a0001c0001t0009g0159a0001c0001t0012g0216others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.193+18102_193+1811 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(5): Show |
7 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(4): Show | 7 | HG01099.hp1 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+18100_193+1811 others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(7): Show |
1 | a0001c0001t0013g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.193+18098_193+1811 others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(9): Show |
4 | a0001c0001t0009g0241a0001c0001t0017g0139a0001c0001t0118g0242others(1): Show | 4 | HG02970.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+18096_193+1811 others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
A | AACACACA others(11): Show |
2 | a0001c0001t0016g0012a0001c0001t0093g0111 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.193+18094_193+1811 others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
AACAC | A | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+18108_193+1811 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
AACACACA others(1): Show |
A | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+18104_193+1811 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898341
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0119g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.193+18102_193+1811 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898341 | ||||||
| chr13:101898377
|
T | C | 4 | a0001c0001t0015g0114a0001c0001t0016g0012a0001c0001t0066g0112others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+18076A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898377 | ||||||
| chr13:101898415
|
C | T | 116 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.193+18038G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898415 | ||||||
| chr13:101898685
|
A | G | 113 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.193+17768T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898685 | ||||||
| chr13:101898970
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+17483G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101898970 | ||||||
| chr13:101899045
|
G | A | 2 | a0001c0001t0132g0184a0001c0001t0135g0183 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.193+17408C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899045 | ||||||
| chr13:101899063
|
A | G | 1 | a0001c0001t0073g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.193+17390T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899063 | ||||||
| chr13:101899133
|
T | C | 265 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.193+17320A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899133 | ||||||
| chr13:101899206
|
G | GA | 138 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.193+17246dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899206 | ||||||
| chr13:101899228
|
C | A | 7 | a0001c0001t0016g0012a0001c0001t0017g0139a0001c0001t0046g0148others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+17225G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899228 | ||||||
| chr13:101899332
|
T | C | 1 | a0001c0001t0031g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.193+17121A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899332 | ||||||
| chr13:101899334
|
C | T | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+17119G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899334 | ||||||
| chr13:101899501
|
T | C | 4 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+16952A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899501 | ||||||
| chr13:101899516
|
A | G | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+16937T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899516 | ||||||
| chr13:101899576
|
G | A | 3 | a0001c0001t0150g0146a0001c0001t0151g0147a0001c0001t0154g0145 | 3 | HG02109.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193+16877C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899576 | ||||||
| chr13:101899717
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.193+16736G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899717 | ||||||
| chr13:101899889
|
C | G | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+16564G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101899889 | ||||||
| chr13:101900020
|
T | C | 113 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.193+16433A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900020 | ||||||
| chr13:101900038
|
T | C | 5 | a0001c0001t0019g0227a0001c0001t0048g0206a0001c0001t0049g0218others(2): Show | 5 | HG02280.hp1 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+16415A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900038 | ||||||
| chr13:101900075
|
T | A | 5 | a0001c0001t0017g0136a0001c0001t0102g0138a0001c0001t0103g0134others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+16378A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900075 | ||||||
| chr13:101900153
|
T | G | 1 | a0001c0001t0009g0255 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.193+16300A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900153 | ||||||
| chr13:101900431
|
G | A | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+16022C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900431 | ||||||
| chr13:101900466
|
C | T | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+15987G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900466 | ||||||
| chr13:101900469
|
C | T | 6 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+15984G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900469 | ||||||
| chr13:101900540
|
C | T | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+15913G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900540 | ||||||
| chr13:101900623
|
G | A | 1 | a0001c0001t0158g0264 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.193+15830C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900623 | ||||||
| chr13:101900641
|
G | T | 2 | a0001c0001t0130g0219a0001c0001t0147g0220 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193+15812C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900641 | ||||||
| chr13:101900739
|
G | C | 1 | a0001c0001t0037g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.193+15714C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900739 | ||||||
| chr13:101900752
|
A | G | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+15701T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900752 | ||||||
| chr13:101900898
|
G | T | 112 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(109): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.193+15555C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900898 | ||||||
| chr13:101900915
|
TATC | T | 6 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0102g0138others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+15535_193+1553 others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900915 | ||||||
| chr13:101900972
|
A | C | 131 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.193+15481T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101900972 | ||||||
| chr13:101901199
|
GA | G | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+15253delT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901199 | ||||||
| chr13:101901255
|
G | T | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+15198C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901255 | ||||||
| chr13:101901330
|
G | C | 1 | a0001c0001t0065g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193+15123C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901330 | ||||||
| chr13:101901600
|
A | T | 1 | a0001c0001t0085g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.193+14853T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901600 | ||||||
| chr13:101901803
|
A | G | 3 | a0001c0001t0150g0146a0001c0001t0151g0147a0001c0001t0154g0145 | 3 | HG02109.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193+14650T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901803 | ||||||
| chr13:101901836
|
A | T | 6 | a0001c0001t0023g0164a0001c0001t0047g0165a0001c0001t0079g0013others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+14617T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901836 | ||||||
| chr13:101901860
|
T | C | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+14593A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901860 | ||||||
| chr13:101901877
|
T | C | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+14576A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901877 | ||||||
| chr13:101901999
|
T | G | 2 | a0001c0001t0045g0214a0001c0001t0045g0215 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.193+14454A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101901999 | ||||||
| chr13:101902031
|
T | C | 133 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.193+14422A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902031 | ||||||
| chr13:101902074
|
C | T | 1 | a0001c0001t0114g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.193+14379G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902074 | ||||||
| chr13:101902286
|
T | G | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+14167A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902286 | ||||||
| chr13:101902342
|
T | G | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+14111A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902342 | ||||||
| chr13:101902549
|
T | C | 1 | a0001c0001t0069g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.193+13904A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902549 | ||||||
| chr13:101902617
|
C | A | 2 | a0001c0001t0016g0010a0001c0001t0099g0011 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.193+13836G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902617 | ||||||
| chr13:101902738
|
G | T | 1 | a0001c0001t0007g0042 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.193+13715C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902738 | ||||||
| chr13:101902794
|
G | A | 1 | a0001c0001t0147g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193+13659C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902794 | ||||||
| chr13:101902842
|
G | T | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+13611C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902842 | ||||||
| chr13:101902843
|
G | T | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+13610C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902843 | ||||||
| chr13:101902844
|
C | A | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+13609G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902844 | ||||||
| chr13:101902845
|
A | G | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+13608T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902845 | ||||||
| chr13:101902846
|
C | A | 1 | a0001c0001t0008g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.193+13607G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902846 | ||||||
| chr13:101902932
|
C | G | 1 | a0001c0001t0070g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.193+13521G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101902932 | ||||||
| chr13:101903122
|
C | T | 141 | a0001c0001t0001g0016a0001c0001t0008g0151a0001c0001t0008g0152others(138): Show | 141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.193+13331G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903122 | ||||||
| chr13:101903238
|
G | GGT | 5 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(2): Show | 5 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+13213_193+1321 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903238 | ||||||
| chr13:101903238
|
G | GGTGT | 95 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(92): Show | 95 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.193+13211_193+1321 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903238 | ||||||
| chr13:101903238
|
G | GGTGTGT | 14 | a0001c0001t0011g0223a0001c0001t0023g0164a0001c0001t0039g0185others(11): Show | 14 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+13209_193+1321 others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903238 | ||||||
| chr13:101903238
|
G | GGTGTGTG others(1): Show |
9 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0107g0175others(6): Show | 9 | HG00280.hp1 HG01952.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.193+13207_193+1321 others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903238 | ||||||
| chr13:101903238
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.193+13205_193+1321 others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903238 | ||||||
| chr13:101903418
|
A | G | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+13035T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903418 | ||||||
| chr13:101903419
|
T | A | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+13034A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903419 | ||||||
| chr13:101903484
|
C | T | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+12969G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903484 | ||||||
| chr13:101903515
|
A | T | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+12938T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903515 | ||||||
| chr13:101903522
|
T | A | 1 | a0001c0001t0111g0202 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.193+12931A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903522 | ||||||
| chr13:101903541
|
C | CT | 7 | a0001c0001t0016g0012a0001c0001t0046g0148a0001c0001t0093g0111others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+12911dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903541 | ||||||
| chr13:101903574
|
G | A | 1 | a0001c0001t0024g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.193+12879C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903574 | ||||||
| chr13:101903765
|
G | A | 3 | a0001c0001t0126g0161a0001c0001t0137g0240a0001c0001t0143g0239 | 3 | HG00642.hp2 HG01099.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.193+12688C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903765 | ||||||
| chr13:101903839
|
A | G | 1 | a0001c0001t0107g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193+12614T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903839 | ||||||
| chr13:101903865
|
T | TTGTA | 11 | a0001c0001t0011g0235a0001c0001t0012g0230a0001c0001t0012g0237others(8): Show | 11 | HG01175.hp2 HG01255.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+12584_193+1258 others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903865 | ||||||
| chr13:101903879
|
G | A | 1 | a0001c0001t0012g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.193+12574C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101903879 | ||||||
| chr13:101904002
|
G | C | 163 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0008g0151others(160): Show | 163 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.193+12451C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904002 | ||||||
| chr13:101904084
|
C | A | 1 | a0001c0001t0008g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.193+12369G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904084 | ||||||
| chr13:101904148
|
C | T | 69 | a0001c0001t0001g0033a0001c0001t0001g0075a0001c0001t0001g0127others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.193+12305G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904148 | ||||||
| chr13:101904164
|
C | A | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+12289G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904164 | ||||||
| chr13:101904248
|
G | C | 2 | a0001c0001t0016g0012a0001c0001t0162g0265 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193+12205C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904248 | ||||||
| chr13:101904250
|
G | C | 1 | a0001c0001t0046g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+12203C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904250 | ||||||
| chr13:101904303
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+12150G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904303 | ||||||
| chr13:101904307
|
T | C | 37 | a0001c0001t0001g0075a0001c0001t0001g0127a0001c0001t0002g0055others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.193+12146A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904307 | ||||||
| chr13:101904322
|
C | T | 28 | a0001c0001t0008g0173a0001c0001t0010g0248a0001c0001t0010g0249others(25): Show | 28 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.193+12131G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904322 | ||||||
| chr13:101904593
|
A | T | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.193+11860T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904593 | ||||||
| chr13:101904656
|
T | C | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+11797A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904656 | ||||||
| chr13:101904669
|
G | C | 1 | a0001c0001t0010g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193+11784C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101904669 | ||||||
| chr13:101905009
|
T | C | 1 | a0001c0001t0064g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.193+11444A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905009 | ||||||
| chr13:101905056
|
C | T | 3 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243 | 3 | HG02970.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.193+11397G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905056 | ||||||
| chr13:101905131
|
G | A | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193+11322C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905131 | ||||||
| chr13:101905162
|
C | T | 3 | a0001c0001t0150g0146a0001c0001t0151g0147a0001c0001t0154g0145 | 3 | HG02109.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193+11291G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905162 | ||||||
| chr13:101905246
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.193+11207G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905246 | ||||||
| chr13:101905290
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.193+11163A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905290 | ||||||
| chr13:101905431
|
T | C | 1 | a0001c0001t0077g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.193+11022A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905431 | ||||||
| chr13:101905532
|
T | TCA | 8 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+10919_193+1092 others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905532 | ||||||
| chr13:101905670
|
C | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+10783G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905670 | ||||||
| chr13:101905738
|
T | C | 3 | a0001c0001t0018g0221a0001c0001t0117g0229a0001c0001t0142g0228 | 3 | HG00408.hp2 NA18969.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.193+10715A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101905738 | ||||||
| chr13:101906058
|
A | G | 11 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+10395T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906058 | ||||||
| chr13:101906071
|
C | T | 1 | a0001c0001t0035g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193+10382G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906071 | ||||||
| chr13:101906089
|
C | T | 10 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+10364G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906089 | ||||||
| chr13:101906135
|
A | T | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+10318T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906135 | ||||||
| chr13:101906182
|
T | A | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+10271A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906182 | ||||||
| chr13:101906279
|
C | A | 1 | a0001c0001t0017g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+10174G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906279 | ||||||
| chr13:101906365
|
G | A | 2 | a0001c0001t0007g0042a0001c0001t0007g0043 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.193+10088C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906365 | ||||||
| chr13:101906382
|
T | G | 8 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+10071A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906382 | ||||||
| chr13:101906498
|
C | T | 1 | a0001c0001t0076g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.193+9955G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906498 | ||||||
| chr13:101906582
|
A | G | 116 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0008g0173others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.193+9871T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906582 | ||||||
| chr13:101906613
|
T | C | 1 | a0001c0001t0058g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193+9840A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906613 | ||||||
| chr13:101906774
|
A | G | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+9679T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906774 | ||||||
| chr13:101906808
|
A | G | 8 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+9645T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906808 | ||||||
| chr13:101906876
|
T | G | 4 | a0001c0001t0102g0138a0001c0001t0103g0134a0001c0001t0104g0137others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+9577A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101906876 | ||||||
| chr13:101907084
|
G | A | 1 | a0001c0001t0092g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.193+9369C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907084 | ||||||
| chr13:101907330
|
T | G | 1 | a0001c0001t0007g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.193+9123A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907330 | ||||||
| chr13:101907373
|
G | A | 1 | a0001c0001t0021g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.193+9080C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907373 | ||||||
| chr13:101907418
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.193+9035C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907418 | ||||||
| chr13:101907448
|
A | C | 8 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+9005T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907448 | ||||||
| chr13:101907501
|
A | G | 156 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0008g0151others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.193+8952T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907501 | ||||||
| chr13:101907548
|
C | T | 6 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+8905G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907548 | ||||||
| chr13:101907549
|
C | T | 3 | a0001c0001t0018g0236a0001c0001t0116g0246a0001c0001t0120g0245 | 3 | HG02698.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.193+8904G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907549 | ||||||
| chr13:101907570
|
C | G | 2 | a0001c0001t0058g0068a0001c0001t0100g0084 | 2 | HG01106.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.193+8883G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907570 | ||||||
| chr13:101907690
|
C | T | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.193+8763G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907690 | ||||||
| chr13:101907886
|
C | A | 6 | a0001c0001t0023g0164a0001c0001t0047g0165a0001c0001t0079g0013others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+8567G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907886 | ||||||
| chr13:101907939
|
A | T | 6 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0102g0138others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+8514T>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101907939 | ||||||
| chr13:101908039
|
T | C | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+8414A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908039 | ||||||
| chr13:101908213
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+8240G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908213 | ||||||
| chr13:101908260
|
T | C | 116 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0008g0173others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.193+8193A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908260 | ||||||
| chr13:101908298
|
C | T | 1 | a0001c0001t0005g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.193+8155G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908298 | ||||||
| chr13:101908576
|
C | T | 4 | a0001c0001t0045g0214a0001c0001t0045g0215a0001c0001t0047g0213others(1): Show | 4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+7877G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908576 | ||||||
| chr13:101908601
|
A | G | 6 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0102g0138others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+7852T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908601 | ||||||
| chr13:101908642
|
T | C | 13 | a0001c0001t0011g0235a0001c0001t0012g0230a0001c0001t0012g0237others(10): Show | 13 | HG01175.hp2 HG01255.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+7811A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908642 | ||||||
| chr13:101908901
|
G | C | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193+7552C>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908901 | ||||||
| chr13:101908924
|
A | G | 2 | a0001c0001t0016g0010a0001c0001t0099g0011 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.193+7529T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101908924 | ||||||
| chr13:101909145
|
T | G | 1 | a0001c0001t0062g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193+7308A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909145 | ||||||
| chr13:101909198
|
A | G | 110 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0008g0173others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.193+7255T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909198 | ||||||
| chr13:101909254
|
A | G | 8 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+7199T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909254 | ||||||
| chr13:101909437
|
GAACAGAC others(8): Show |
G | 1 | a0001c0001t0024g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.193+7001_193+7015d others(17): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909437 | ||||||
| chr13:101909527
|
C | T | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6926G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909527 | ||||||
| chr13:101909685
|
G | A | 87 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.193+6768C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909685 | ||||||
| chr13:101909746
|
A | C | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.193+6707T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909746 | ||||||
| chr13:101909750
|
C | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0082 | 2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.193+6703G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909750 | ||||||
| chr13:101909755
|
G | T | 2 | a0001c0001t0015g0114a0001c0001t0066g0112 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.193+6698C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909755 | ||||||
| chr13:101909796
|
T | G | 34 | a0001c0001t0008g0208a0001c0001t0009g0179a0001c0001t0009g0203others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.193+6657A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909796 | ||||||
| chr13:101909927
|
T | C | 1 | a0001c0001t0103g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193+6526A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909927 | ||||||
| chr13:101909948
|
T | C | 1 | a0001c0001t0019g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.193+6505A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101909948 | ||||||
| chr13:101910017
|
C | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6436G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910017 | ||||||
| chr13:101910020
|
A | G | 5 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+6433T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910020 | ||||||
| chr13:101910043
|
G | T | 6 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+6410C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910043 | ||||||
| chr13:101910099
|
G | T | 6 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0102g0138others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+6354C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910099 | ||||||
| chr13:101910107
|
G | T | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+6346C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910107 | ||||||
| chr13:101910121
|
A | C | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6332T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910121 | ||||||
| chr13:101910232
|
A | G | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6221T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910232 | ||||||
| chr13:101910248
|
TAAATA | T | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+6200_193+6204d others(7): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910248 | ||||||
| chr13:101910512
|
A | G | 2 | a0001c0001t0050g0001a0001c0001t0051g0002 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193+5941T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910512 | ||||||
| chr13:101910537
|
T | C | 1 | a0001c0001t0006g0083 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.193+5916A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910537 | ||||||
| chr13:101910657
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.193+5796C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910657 | ||||||
| chr13:101910705
|
C | T | 1 | a0001c0001t0093g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+5748G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910705 | ||||||
| chr13:101910837
|
C | CGT | 16 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0003g0030others(13): Show | 16 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.193+5614_193+5615d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
C | CGTGTGT | 3 | a0001c0001t0001g0029a0001c0001t0070g0028a0001c0001t0155g0149 | 3 | HG02040.hp2 NA19074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.193+5610_193+5615d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGT | C | 16 | a0001c0001t0002g0065a0001c0001t0006g0059a0001c0001t0008g0151others(13): Show | 16 | HG00621.hp1 HG01106.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.193+5614_193+5615d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGT | C | 32 | a0001c0001t0001g0075a0001c0001t0003g0076a0001c0001t0004g0070others(29): Show | 32 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.193+5612_193+5615d others(6): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGT | C | 26 | a0001c0001t0001g0127a0001c0001t0004g0088a0001c0001t0006g0085others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.193+5610_193+5615d others(8): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(1): Show |
C | 46 | a0001c0001t0001g0093a0001c0001t0002g0096a0001c0001t0002g0098others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+5608_193+5615d others(10): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(3): Show |
C | 23 | a0001c0001t0001g0016a0001c0001t0002g0109a0001c0001t0008g0208others(20): Show | 23 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+5606_193+5615d others(12): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(5): Show |
C | 33 | a0001c0001t0002g0101a0001c0001t0005g0102a0001c0001t0005g0103others(30): Show | 33 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.193+5604_193+5615d others(14): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(7): Show |
C | 18 | a0001c0001t0002g0104a0001c0001t0008g0173a0001c0001t0011g0223others(15): Show | 18 | HG00408.hp2 HG00597.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.193+5602_193+5615d others(16): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(9): Show |
C | 6 | a0001c0001t0008g0233a0001c0001t0011g0235a0001c0001t0015g0124others(3): Show | 6 | HG01175.hp2 HG01255.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+5600_193+5615d others(18): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(11): Show |
C | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+5598_193+5615d others(20): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(13): Show |
C | 7 | a0001c0001t0012g0237a0001c0001t0018g0236a0001c0001t0093g0111others(4): Show | 7 | HG02630.hp1 HG02698.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+5596_193+5615d others(22): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(15): Show |
C | 3 | a0001c0001t0015g0121a0001c0001t0016g0010a0001c0001t0099g0011 | 3 | HG01516.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.193+5594_193+5615d others(24): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(17): Show |
C | 4 | a0001c0001t0009g0255a0001c0001t0021g0170a0001c0001t0046g0169others(1): Show | 4 | HG01074.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+5592_193+5615d others(26): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(21): Show |
C | 1 | a0001c0001t0154g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193+5588_193+5615d others(30): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910837
|
CGTGTGTG others(23): Show |
C | 3 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147 | 3 | HG02109.hp1 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.193+5586_193+5615d others(32): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910837 | ||||||
| chr13:101910882
|
GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0003g0106a0001c0001t0056g0107 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.193+5560_193+5570d others(13): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101910882 | ||||||
| chr13:101911057
|
T | C | 5 | a0001c0001t0029g0115a0001c0001t0091g0117a0001c0001t0094g0119others(2): Show | 5 | HG01192.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+5396A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911057 | ||||||
| chr13:101911149
|
A | G | 1 | a0001c0001t0026g0027 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.193+5304T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911149 | ||||||
| chr13:101911191
|
T | A | 1 | a0001c0001t0125g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193+5262A>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911191 | ||||||
| chr13:101911487
|
A | G | 1 | a0001c0001t0027g0026 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193+4966T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911487 | ||||||
| chr13:101911525
|
C | A | 1 | a0001c0001t0031g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.193+4928G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911525 | ||||||
| chr13:101911538
|
T | C | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+4915A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911538 | ||||||
| chr13:101911613
|
T | C | 2 | a0001c0001t0158g0264a0001c0001t0161g0263 | 2 | HG01081.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.193+4840A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911613 | ||||||
| chr13:101911731
|
A | C | 3 | a0001c0001t0008g0173a0001c0001t0108g0172a0001c0001t0112g0171 | 3 | NA18971.hp1 NA18988.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.193+4722T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911731 | ||||||
| chr13:101911812
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.193+4641C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911812 | ||||||
| chr13:101911886
|
G | T | 1 | a0001c0001t0061g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.193+4567C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101911886 | ||||||
| chr13:101912004
|
GT | G | 120 | a0001c0001t0001g0016a0001c0001t0008g0173a0001c0001t0008g0208others(117): Show | 120 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.193+4448delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912004 | ||||||
| chr13:101912004
|
GTT | G | 7 | a0001c0001t0016g0012a0001c0001t0017g0135a0001c0001t0017g0136others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4447_193+4448d others(4): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912004 | ||||||
| chr13:101912018
|
T | C | 2 | a0001c0001t0137g0240a0001c0001t0143g0239 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.193+4435A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912018 | ||||||
| chr13:101912289
|
C | T | 1 | a0001c0001t0069g0024 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.193+4164G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912289 | ||||||
| chr13:101912392
|
A | G | 4 | a0001c0001t0046g0148a0001c0001t0150g0146a0001c0001t0151g0147others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4061T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912392 | ||||||
| chr13:101912762
|
A | C | 1 | a0001c0001t0030g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193+3691T>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912762 | ||||||
| chr13:101912805
|
C | A | 3 | a0001c0001t0009g0241a0001c0001t0118g0242a0001c0001t0129g0243 | 3 | HG02970.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.193+3648G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912805 | ||||||
| chr13:101912841
|
G | A | 5 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+3612C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912841 | ||||||
| chr13:101912889
|
A | G | 5 | a0001c0001t0046g0148a0001c0001t0093g0111a0001c0001t0150g0146others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+3564T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912889 | ||||||
| chr13:101912918
|
T | C | 107 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.193+3535A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912918 | ||||||
| chr13:101912929
|
T | C | 1 | a0001c0001t0019g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193+3524A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912929 | ||||||
| chr13:101912977
|
AT | A | 18 | a0001c0001t0001g0016a0001c0001t0028g0018a0001c0001t0028g0019others(15): Show | 18 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.193+3475delA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101912977 | ||||||
| chr13:101913171
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.193+3282C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913171 | ||||||
| chr13:101913231
|
G | T | 1 | a0001c0001t0131g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.193+3222C>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913231 | ||||||
| chr13:101913327
|
C | G | 1 | a0001c0001t0162g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+3126G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913327 | ||||||
| chr13:101913370
|
C | T | 32 | a0001c0001t0001g0016a0001c0001t0016g0012a0001c0001t0017g0135others(29): Show | 32 | HG01192.hp2 HG01891.hp1 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.193+3083G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913370 | ||||||
| chr13:101913397
|
C | A | 1 | a0001c0001t0016g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+3056G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913397 | ||||||
| chr13:101913469
|
T | C | 128 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0008g0173others(125): Show | 128 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.193+2984A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913469 | ||||||
| chr13:101913499
|
A | AT | 163 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0008g0151others(160): Show | 163 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.193+2953dupA | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913499 | ||||||
| chr13:101913520
|
C | A | 8 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0017g0139others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2933G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913520 | ||||||
| chr13:101913650
|
T | G | 2 | a0001c0001t0116g0246a0001c0001t0120g0245 | 2 | HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.193+2803A>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913650 | ||||||
| chr13:101913711
|
T | TA | 8 | a0001c0001t0008g0151a0001c0001t0008g0152a0001c0001t0010g0153others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2741dupT | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913711 | ||||||
| chr13:101913796
|
C | T | 1 | a0001c0001t0126g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.193+2657G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101913796 | ||||||
| chr13:101914008
|
T | C | 6 | a0001c0001t0029g0115a0001c0001t0081g0120a0001c0001t0091g0117others(3): Show | 6 | HG01192.hp2 HG01884.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+2445A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914008 | ||||||
| chr13:101914098
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.193+2355A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914098 | ||||||
| chr13:101914216
|
T | C | 8 | a0001c0001t0010g0248a0001c0001t0010g0249a0001c0001t0020g0250others(5): Show | 8 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2237A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914216 | ||||||
| chr13:101914321
|
T | C | 1 | a0001c0001t0074g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.193+2132A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914321 | ||||||
| chr13:101914464
|
A | G | 7 | a0001c0001t0009g0159a0001c0001t0023g0157a0001c0001t0023g0158others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+1989T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914464 | ||||||
| chr13:101914539
|
C | A | 1 | a0001c0001t0026g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.193+1914G>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914539 | ||||||
| chr13:101914720
|
C | T | 5 | a0001c0001t0025g0007a0001c0001t0025g0008a0001c0001t0053g0005others(2): Show | 5 | NA18978.hp2 NA18986.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+1733G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914720 | ||||||
| chr13:101914761
|
A | G | 8 | a0001c0001t0024g0259a0001c0001t0024g0260a0001c0001t0024g0261others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1692T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101914761 | ||||||
| chr13:101915182
|
T | C | 1 | a0001c0001t0009g0255 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.193+1271A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101915182 | ||||||
| chr13:101915459
|
T | C | 114 | a0001c0001t0008g0173a0001c0001t0008g0208a0001c0001t0008g0233others(111): Show | 114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.193+994A>G | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101915459 | ||||||
| chr13:101915624
|
A | AAAG | 265 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0033others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.193+826_193+828dup others(3): Show |
FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101915624 | ||||||
| chr13:101915953
|
G | A | 1 | a0001c0001t0071g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.193+500C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101915953 | ||||||
| chr13:101916210
|
A | G | 11 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+243T>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916210 | ||||||
| chr13:101916260
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0038g0125a0001c0001t0064g0126others(1): Show | 4 | HG01175.hp1 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+193C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916260 | ||||||
| chr13:101916273
|
G | A | 1 | a0001c0001t0096g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193+180C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916273 | ||||||
| chr13:101916306
|
C | G | 2 | a0001c0001t0050g0001a0001c0001t0051g0002 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193+147G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916306 | ||||||
| chr13:101916307
|
C | G | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0144others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+146G>C | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916307 | ||||||
| chr13:101916335
|
G | A | 7 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0017g0139others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+118C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916335 | ||||||
| chr13:101916341
|
C | T | 1 | a0001c0001t0152g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.193+112G>A | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916341 | ||||||
| chr13:101916351
|
G | A | 7 | a0001c0001t0017g0135a0001c0001t0017g0136a0001c0001t0017g0139others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+102C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916351 | ||||||
| chr13:101916407
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0016g0130a0001c0001t0083g0131 | 3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.193+46C>T | FGF14 | ENSG00000102466.17 | transcript | ENST00000376143.5 | protein_coding | 1/4 | chr13 | 101916407 |