Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2255 |
|---|---|
| ensemblid | ENSG00000070193.5 |
| hgncid | 3666 |
| symbol | FGF10 |
| name | fibroblast growth factor 10 |
| refseq_nuc | NM_004465.2 |
| refseq_prot | NP_004456.1 |
| ensembl_nuc | ENST00000264664.5 |
| ensembl_prot | ENSP00000264664.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 44300247 |
| end | 44389420 |
| strand | - |
| ver | v1.2 |
| region | chr5:44300247-44389420 |
| region5000 | chr5:44295247-44394420 |
| regionname0 | FGF10_chr5_44300247_44389420 |
| regionname5000 | FGF10_chr5_44295247_44394420 |
| 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 | 208 | 348 | 85 | 61 | 158 | 14 | 28 | 130 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0002 | 0/0 | 208 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0003 | 0/0 | 208 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| 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 | 627 | 342 | 80 | 60 | 158 | 14 | 28 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| c0002 | 0/0 | 627 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| c0003 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| c0004 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| 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 | 5476 | 47 | 2 | 9 | 30 | 1 | 5 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0002 | 0/0 | 5487 | 41 | 0 | 7 | 25 | 3 | 6 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0003 | 0/1 | 5483 | 32 | 1 | 6 | 23 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0004 | 0/0 | 5491 | 22 | 9 | 0 | 13 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0005 | 0/0 | 5483 | 18 | 12 | 2 | 0 | 0 | 4 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0006 | 0/0 | 5491 | 17 | 1 | 5 | 6 | 3 | 2 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0007 | 0/0 | 5487 | 15 | 6 | 1 | 8 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0008 | 0/0 | 5483 | 8 | 0 | 6 | 0 | 1 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0009 | 0/0 | 5490 | 7 | 6 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0010 | 0/0 | 5527 | 7 | 0 | 2 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0011 | 0/0 | 5535 | 7 | 0 | 0 | 7 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0012 | 0/0 | 5476 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0013 | 0/0 | 5480 | 6 | 2 | 2 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0014 | 0/0 | 5495 | 6 | 0 | 0 | 6 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0015 | 0/0 | 5479 | 5 | 0 | 3 | 1 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0016 | 0/0 | 5495 | 5 | 0 | 0 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0017 | 0/0 | 5472 | 5 | 2 | 1 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0018 | 0/0 | 5484 | 5 | 3 | 1 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0019 | 0/0 | 5531 | 5 | 0 | 0 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0020 | 0/0 | 5462 | 4 | 4 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0021 | 0/0 | 5499 | 3 | 0 | 0 | 3 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0022 | 0/0 | 5474 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0023 | 0/0 | 5488 | 3 | 0 | 1 | 0 | 2 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0024 | 0/0 | 5486 | 3 | 0 | 3 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0025 | 0/0 | 5483 | 3 | 0 | 2 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0026 | 0/0 | 5483 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0027 | 0/0 | 5486 | 2 | 0 | 1 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0028 | 0/0 | 5476 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0029 | 0/0 | 5479 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0030 | 0/0 | 5483 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0031 | 1/0 | 5487 | 2 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0032 | 0/0 | 5519 | 2 | 0 | 0 | 1 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0033 | 0/0 | 5523 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0034 | 0/0 | 5531 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0035 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0036 | 0/0 | 5475 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0037 | 0/0 | 5479 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0038 | 0/0 | 5487 | 2 | 0 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0039 | 0/0 | 5487 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0040 | 0/0 | 5491 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0041 | 0/0 | 5474 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0042 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0043 | 0/0 | 5486 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0044 | 0/0 | 5494 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0045 | 0/0 | 5486 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0046 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0047 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0048 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0049 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0050 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0051 | 0/0 | 5487 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0052 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0053 | 0/0 | 5478 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0054 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0055 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0056 | 0/0 | 5490 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0057 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0058 | 0/0 | 5476 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0059 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0060 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0061 | 0/0 | 5488 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0062 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0063 | 0/0 | 5492 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0064 | 0/0 | 5467 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0065 | 0/0 | 5527 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0066 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0067 | 0/0 | 5476 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0068 | 0/0 | 5490 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0069 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0070 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0071 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0072 | 0/0 | 5479 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0073 | 0/0 | 5479 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0074 | 0/0 | 5483 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0075 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| t0076 | 0/0 | 5460 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| 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 | 2 | 1 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| 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 | 627 | 342 | 80 | 60 | 158 | 14 | 28 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0002 | 0/0 | 627 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0002c0003 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0003c0004 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6102 | 47 | 2 | 9 | 30 | 1 | 5 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0002 | 0/0 | 6113 | 41 | 0 | 7 | 25 | 3 | 6 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0003 | 0/1 | 6109 | 32 | 1 | 6 | 23 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0004 | 0/0 | 6117 | 22 | 9 | 0 | 13 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0005 | 0/0 | 6109 | 12 | 7 | 1 | 0 | 0 | 4 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0006 | 0/0 | 6117 | 17 | 1 | 5 | 6 | 3 | 2 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0007 | 0/0 | 6113 | 15 | 6 | 1 | 8 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0008 | 0/0 | 6109 | 8 | 0 | 6 | 0 | 1 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0009 | 0/0 | 6116 | 7 | 6 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0010 | 0/0 | 6153 | 7 | 0 | 2 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0011 | 0/0 | 6161 | 7 | 0 | 0 | 7 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0012 | 0/0 | 6102 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0013 | 0/0 | 6106 | 6 | 2 | 2 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0014 | 0/0 | 6121 | 6 | 0 | 0 | 6 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0015 | 0/0 | 6105 | 5 | 0 | 3 | 1 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0016 | 0/0 | 6121 | 5 | 0 | 0 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0017 | 0/0 | 6098 | 5 | 2 | 1 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0018 | 0/0 | 6110 | 5 | 3 | 1 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0019 | 0/0 | 6157 | 5 | 0 | 0 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0020 | 0/0 | 6088 | 4 | 4 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0021 | 0/0 | 6125 | 3 | 0 | 0 | 3 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0022 | 0/0 | 6100 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0023 | 0/0 | 6114 | 3 | 0 | 1 | 0 | 2 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0024 | 0/0 | 6112 | 3 | 0 | 3 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0025 | 0/0 | 6109 | 3 | 0 | 2 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0026 | 0/0 | 6109 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0027 | 0/0 | 6112 | 2 | 0 | 1 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0028 | 0/0 | 6102 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0029 | 0/0 | 6105 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0030 | 0/0 | 6109 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0031 | 1/0 | 6113 | 2 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0032 | 0/0 | 6145 | 2 | 0 | 0 | 1 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0033 | 0/0 | 6149 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0034 | 0/0 | 6157 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0035 | 0/0 | 6117 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0036 | 0/0 | 6101 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0037 | 0/0 | 6105 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0038 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0039 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0040 | 0/0 | 6117 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0041 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0042 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0043 | 0/0 | 6112 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0044 | 0/0 | 6120 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0045 | 0/0 | 6112 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0046 | 0/0 | 6110 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0047 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0048 | 0/0 | 6161 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0049 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0051 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0052 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0053 | 0/0 | 6104 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0054 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0055 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0056 | 0/0 | 6116 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0057 | 0/0 | 6090 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0058 | 0/0 | 6102 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0059 | 0/0 | 6102 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0060 | 0/0 | 6102 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0061 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0062 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0063 | 0/0 | 6118 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0064 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0065 | 0/0 | 6153 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0066 | 0/0 | 6165 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0067 | 0/0 | 6102 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0068 | 0/0 | 6116 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0069 | 0/0 | 6117 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0070 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0071 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0072 | 0/0 | 6105 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0073 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0074 | 0/0 | 6109 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0075 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0001t0076 | 0/0 | 6086 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0001c0002t0005 | 0/0 | 6109 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0002c0003t0050 | 0/0 | 6125 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| a0003c0004t0038 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | copy fasta | chr5 | 44295247 | 44394420 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0021g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0021g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0022g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0023g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0023g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0024g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0024g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0024g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0025g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0025g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0026g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0026g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0026g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0027g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0027g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0028g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0028g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0029g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0030g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0030g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0031g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0031g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0032g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0032g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0033g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0033g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0034g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0034g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0035g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0035g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0036g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0036g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0037g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0037g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0038g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0039g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0039g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0040g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0040g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0041g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0042g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0043g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0044g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0045g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0046g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0047g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0048g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0049g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0051g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0052g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0053g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0054g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0055g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0056g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0057g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0058g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0059g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0060g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0061g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0062g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0063g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0064g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0065g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0066g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0067g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0068g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0069g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0070g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0071g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0072g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0073g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0074g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0075g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0076g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0002c0003t0050g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0003c0004t0038g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | GBR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0095 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00280 | hp2 | a0001 | c0001 | t0015 | g0206 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0217 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00323 | hp2 | a0001 | c0001 | t0025 | g0040 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0308 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00639 | hp1 | a0001 | c0001 | t0068 | g0122 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0253 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00673 | hp1 | a0001 | c0001 | t0011 | g0272 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0099 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0098 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00741 | hp1 | a0001 | c0001 | t0017 | g0306 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01070 | hp1 | a0001 | c0001 | t0024 | g0121 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0214 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01074 | hp2 | a0001 | c0001 | t0013 | g0300 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01099 | hp1 | a0001 | c0001 | t0076 | g0341 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0126 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01106 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01109 | hp2 | a0001 | c0001 | t0074 | g0110 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0052 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01168 | hp1 | a0001 | c0001 | t0025 | g0002 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0303 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01169 | hp2 | a0001 | c0001 | t0025 | g0002 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01175 | hp1 | a0003 | c0004 | t0038 | g0062 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01175 | hp2 | a0001 | c0001 | t0027 | g0014 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01192 | hp2 | a0001 | c0001 | t0018 | g0103 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01243 | hp1 | a0001 | c0001 | t0023 | g0116 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0127 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01257 | hp1 | a0001 | c0001 | t0033 | g0257 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01257 | hp2 | a0001 | c0001 | t0024 | g0338 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0101 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01258 | hp2 | a0001 | c0001 | t0024 | g0339 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0042 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01346 | hp1 | a0001 | c0001 | t0075 | g0280 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0208 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01358 | hp2 | a0001 | c0001 | t0033 | g0270 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01361 | hp1 | a0001 | c0001 | t0041 | g0013 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01515 | hp1 | a0001 | c0001 | t0027 | g0010 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0004 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0124 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0032 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0004 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01884 | hp1 | a0002 | c0003 | t0050 | g0030 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01891 | hp1 | a0001 | c0001 | t0059 | g0061 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0058 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0205 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01952 | hp2 | a0001 | c0001 | t0010 | g0258 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02055 | hp1 | a0001 | c0001 | t0069 | g0054 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0001 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02056 | hp2 | a0001 | c0001 | t0014 | g0089 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02071 | hp1 | a0001 | c0001 | t0066 | g0181 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0084 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0114 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CDX | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | CDX | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02257 | hp1 | a0001 | c0001 | t0026 | g0248 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0049 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02258 | hp2 | a0001 | c0001 | t0045 | g0016 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02280 | hp1 | a0001 | c0001 | t0073 | g0279 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0296 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02451 | hp1 | a0001 | c0001 | t0020 | g0240 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02523 | hp1 | a0001 | c0001 | t0040 | g0070 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02615 | hp1 | a0001 | c0001 | t0046 | g0028 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02615 | hp2 | a0001 | c0001 | t0030 | g0120 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02622 | hp1 | a0001 | c0001 | t0035 | g0111 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0106 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02683 | hp1 | a0001 | c0001 | t0018 | g0109 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0100 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0104 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02717 | hp2 | a0001 | c0001 | t0042 | g0012 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0337 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0241 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02818 | hp2 | a0001 | c0001 | t0060 | g0219 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0243 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02895 | hp1 | a0001 | c0001 | t0037 | g0119 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02895 | hp2 | a0001 | c0001 | t0061 | g0115 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02896 | hp2 | a0001 | c0001 | t0037 | g0046 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0239 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0112 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0336 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03017 | hp2 | a0001 | c0001 | t0063 | g0107 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03041 | hp2 | a0001 | c0001 | t0035 | g0177 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03098 | hp1 | a0001 | c0001 | t0026 | g0278 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03098 | hp2 | a0001 | c0001 | t0029 | g0135 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03130 | hp1 | a0001 | c0001 | t0064 | g0102 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0183 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03195 | hp1 | a0001 | c0001 | t0052 | g0123 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0050 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0216 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03486 | hp1 | a0001 | c0001 | t0029 | g0139 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03491 | hp1 | a0001 | c0001 | t0056 | g0175 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0290 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0281 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03516 | hp2 | a0001 | c0001 | t0044 | g0021 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03540 | hp1 | a0001 | c0001 | t0055 | g0228 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03579 | hp1 | a0001 | c0001 | t0071 | g0053 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03704 | hp2 | a0001 | c0001 | t0054 | g0171 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03831 | hp1 | a0001 | c0001 | t0072 | g0340 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0159 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04115 | hp1 | a0001 | c0001 | t0053 | g0150 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04115 | hp2 | a0001 | c0001 | t0043 | g0011 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18522 | hp1 | a0001 | c0001 | t0062 | g0178 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18612 | hp1 | a0001 | c0001 | t0038 | g0068 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18612 | hp2 | a0001 | c0001 | t0011 | g0266 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18747 | hp2 | a0001 | c0001 | t0065 | g0264 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0242 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18939 | hp1 | a0001 | c0001 | t0014 | g0063 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18940 | hp2 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18943 | hp2 | a0001 | c0001 | t0070 | g0085 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18946 | hp1 | a0001 | c0001 | t0011 | g0277 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0190 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18947 | hp2 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18948 | hp2 | a0001 | c0001 | t0039 | g0222 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18950 | hp2 | a0001 | c0001 | t0034 | g0274 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18953 | hp1 | a0001 | c0001 | t0021 | g0168 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0235 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18961 | hp1 | a0001 | c0001 | t0036 | g0083 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18964 | hp2 | a0001 | c0001 | t0034 | g0275 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18968 | hp1 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18969 | hp2 | a0001 | c0001 | t0058 | g0317 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18972 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18974 | hp2 | a0001 | c0001 | t0014 | g0088 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18977 | hp1 | a0001 | c0001 | t0021 | g0169 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18977 | hp2 | a0001 | c0001 | t0040 | g0223 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18982 | hp1 | a0001 | c0001 | t0019 | g0254 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18983 | hp1 | a0001 | c0001 | t0015 | g0166 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18983 | hp2 | a0001 | c0001 | t0016 | g0170 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18984 | hp1 | a0001 | c0001 | t0019 | g0265 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18990 | hp1 | a0001 | c0001 | t0010 | g0260 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18993 | hp1 | a0001 | c0001 | t0021 | g0136 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18994 | hp1 | a0001 | c0001 | t0014 | g0078 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18994 | hp2 | a0001 | c0001 | t0032 | g0276 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18995 | hp1 | a0001 | c0001 | t0039 | g0224 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18998 | hp1 | a0001 | c0001 | t0017 | g0316 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18998 | hp2 | a0001 | c0001 | t0019 | g0261 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19004 | hp2 | a0001 | c0001 | t0048 | g0255 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19005 | hp1 | a0001 | c0001 | t0011 | g0256 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0251 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19009 | hp1 | a0001 | c0001 | t0011 | g0269 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0037 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0117 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19043 | hp2 | a0001 | c0001 | t0028 | g0249 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19060 | hp1 | a0001 | c0001 | t0014 | g0066 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19063 | hp1 | a0001 | c0001 | t0049 | g0152 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19063 | hp2 | a0001 | c0001 | t0013 | g0331 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0273 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19067 | hp1 | a0001 | c0001 | t0067 | g0310 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19068 | hp1 | a0001 | c0001 | t0036 | g0072 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19068 | hp2 | a0001 | c0001 | t0010 | g0267 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19070 | hp1 | a0001 | c0001 | t0016 | g0142 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19077 | hp1 | a0001 | c0001 | t0016 | g0167 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19080 | hp1 | a0001 | c0001 | t0017 | g0311 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19080 | hp2 | a0001 | c0001 | t0016 | g0207 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19087 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0262 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20129 | hp1 | a0001 | c0001 | t0047 | g0024 | AFR | ASW | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20805 | hp1 | a0001 | c0001 | t0057 | g0312 | EUR | TSI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20905 | hp1 | a0001 | c0001 | t0051 | g0097 | SAS | GIH | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20905 | hp2 | a0001 | c0001 | t0032 | g0252 | SAS | GIH | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0096 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01123 | hp2 | a0001 | c0001 | t0015 | g0125 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0247 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02486 | hp2 | a0001 | c0001 | t0022 | g0182 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0295 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03471 | hp2 | a0001 | c0001 | t0018 | g0105 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20300 | hp1 | a0001 | c0001 | t0030 | g0211 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA21309 | hp1 | a0001 | c0001 | t0028 | g0250 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0137 | REF | REF | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0031 | g0236 | REF | REF | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44305002
|
T | G | 1 | a0003 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.620A>C | p.His207Pro | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1358/6113 | 620/627 | 207/208 | chr5 | 44305002 | ||
| chr5:44388586
|
C | T | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.97G>A | p.Val33Ile | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/3 | 835/6113 | 97/627 | 33/208 | chr5 | 44388586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44305031
|
G | A | 1 | a0001c0002 | 6 | HG01167.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.591C>T | p.Thr197Thr | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1329/6113 | 591/627 | 197/208 | chr5 | 44305031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44300259
|
T | TTC | 35 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(32): Show | 135 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*4735_*4736insGA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4735 | chr5 | 44300259 | |||||
| chr5:44300266
|
T | A | 1 | a0001c0001t0071 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4729A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4729 | chr5 | 44300266 | |||||
| chr5:44300412
|
C | T | 1 | a0001c0001t0034 | 2 | NA18950.hp2 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4583G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4583 | chr5 | 44300412 | |||||
| chr5:44300545
|
A | G | 1 | a0001c0001t0047 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4450T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4450 | chr5 | 44300545 | |||||
| chr5:44300548
|
A | G | 14 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(11): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*4447T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4447 | chr5 | 44300548 | |||||
| chr5:44300553
|
T | C | 18 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(15): Show | 80 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*4442A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4442 | chr5 | 44300553 | |||||
| chr5:44300805
|
T | C | 1 | a0001c0001t0074 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4190A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4190 | chr5 | 44300805 | |||||
| chr5:44300809
|
T | C | 1 | a0001c0001t0060 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4186A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4186 | chr5 | 44300809 | |||||
| chr5:44300827
|
T | C | 1 | a0001c0001t0058 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4168A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4168 | chr5 | 44300827 | |||||
| chr5:44300843
|
G | A | 1 | a0001c0001t0064 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4152C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4152 | chr5 | 44300843 | |||||
| chr5:44300850
|
G | A | 3 | a0001c0001t0008a0001c0001t0028a0001c0001t0051 | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4145C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 4145 | chr5 | 44300850 | |||||
| chr5:44301009
|
C | G | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*3986G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3986 | chr5 | 44301009 | |||||
| chr5:44301040
|
T | G | 1 | a0001c0001t0070 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3955A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3955 | chr5 | 44301040 | |||||
| chr5:44301065
|
A | G | 4 | a0001c0001t0024a0001c0001t0027a0001c0001t0043others(1): Show | 7 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3930T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3930 | chr5 | 44301065 | |||||
| chr5:44301259
|
T | C | 1 | a0001c0001t0061 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3736A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3736 | chr5 | 44301259 | |||||
| chr5:44301288
|
T | A | 14 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(11): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*3707A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3707 | chr5 | 44301288 | |||||
| chr5:44301463
|
AT | A | 2 | a0001c0001t0008a0001c0001t0051 | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3531delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3531 | chr5 | 44301463 | |||||
| chr5:44301858
|
ATTTTC | A | 8 | a0001c0001t0020a0001c0001t0022a0001c0001t0026others(5): Show | 15 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3132_*3136delGAAA others(1): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3132 | chr5 | 44301858 | |||||
| chr5:44301927
|
C | A | 1 | a0001c0001t0029 | 2 | HG03098.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3068G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3068 | chr5 | 44301927 | |||||
| chr5:44301928
|
G | A | 1 | a0001c0001t0060 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3067C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 3067 | chr5 | 44301928 | |||||
| chr5:44302075
|
A | G | 1 | a0001c0001t0025 | 3 | HG00323.hp2 HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2920T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2920 | chr5 | 44302075 | |||||
| chr5:44302075
|
A | T | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(8): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2920T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2920 | chr5 | 44302075 | |||||
| chr5:44302118
|
CT | C | 6 | a0001c0001t0020a0001c0001t0022a0001c0001t0041others(3): Show | 11 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2876delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2876 | chr5 | 44302118 | |||||
| chr5:44302275
|
T | TTTCCTTG others(29): Show |
1 | a0001c0001t0033 | 2 | HG01257.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2684_*2719dupGGAA others(32): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2719 | chr5 | 44302275 | |||||
| chr5:44302275
|
TTTCCTTG others(1): Show |
T | 3 | a0001c0001t0022a0001c0001t0041a0001c0001t0055 | 5 | HG01361.hp1 HG02486.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2712_*2719delGCAA others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302275 | |||||
| chr5:44302275
|
TTTCCTTG others(13): Show |
T | 1 | a0001c0001t0020 | 4 | HG01891.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2700_*2719delGGAA others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2700 | chr5 | 44302275 | |||||
| chr5:44302282
|
G | C | 2 | a0001c0001t0038a0003c0004t0038 | 2 | HG01175.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2713C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2713 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTC | 13 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(10): Show | 58 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2709_*2712dupGAAG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(1): Show |
3 | a0001c0001t0014a0001c0001t0016a0001c0001t0044 | 12 | HG02056.hp2 HG03516.hp2 NA18939.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2705_*2712dupGAAG others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(5): Show |
2 | a0001c0001t0021a0002c0003t0050 | 4 | HG01884.hp1 NA18953.hp1 NA18977.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2701_*2712dupGAAG others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(33): Show |
1 | a0001c0001t0010 | 7 | HG00639.hp2 HG01952.hp2 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2712_*2713insGAAG others(36): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(37): Show |
2 | a0001c0001t0019a0001c0001t0034 | 7 | NA18950.hp2 NA18964.hp2 NA18968.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2712_*2713insGAAG others(40): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(41): Show |
2 | a0001c0001t0011a0001c0001t0048 | 8 | HG00673.hp1 NA18612.hp2 NA18946.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2712_*2713insGAAG others(44): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
G | GCTTCCTT others(45): Show |
1 | a0001c0001t0066 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712_*2713insGAAG others(48): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2712 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTC | G | 12 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(9): Show | 73 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2709_*2712delGAAG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2709 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(1): Show |
G | 7 | a0001c0001t0013a0001c0001t0015a0001c0001t0029others(4): Show | 18 | HG00280.hp2 HG00544.hp1 HG01074.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2705_*2712delGAAG others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2705 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(5): Show |
G | 8 | a0001c0001t0001a0001c0001t0012a0001c0001t0028others(5): Show | 61 | HG00099.hp1 HG00597.hp2 HG01069.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2701_*2712delGAAG others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2701 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(9): Show |
G | 1 | a0001c0001t0017 | 5 | HG00741.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2697_*2712delGAAG others(12): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2697 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(13): Show |
G | 1 | a0001c0001t0064 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2693_*2712delGAAG others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2693 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(17): Show |
G | 1 | a0001c0001t0057 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2689_*2712delGAAG others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2689 | chr5 | 44302282 | |||||
| chr5:44302282
|
GCTTCCTT others(21): Show |
G | 1 | a0001c0001t0076 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2685_*2712delGAAG others(24): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2685 | chr5 | 44302282 | |||||
| chr5:44302286
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0065 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2708_*2709insCAAG others(36): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2708 | chr5 | 44302286 | |||||
| chr5:44302286
|
C | CCTTCCTT others(25): Show |
1 | a0001c0001t0032 | 2 | NA18994.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2708_*2709insCAAG others(28): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2708 | chr5 | 44302286 | |||||
| chr5:44302471
|
G | A | 2 | a0001c0001t0039a0001c0001t0040 | 4 | HG02523.hp1 NA18948.hp2 NA18977.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2524C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2524 | chr5 | 44302471 | |||||
| chr5:44302765
|
A | G | 1 | a0001c0001t0069 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2230T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2230 | chr5 | 44302765 | |||||
| chr5:44302777
|
AC | A | 4 | a0001c0001t0024a0001c0001t0027a0001c0001t0043others(1): Show | 7 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2217delG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 2217 | chr5 | 44302777 | |||||
| chr5:44303157
|
T | C | 1 | a0001c0001t0043 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1838A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1838 | chr5 | 44303157 | |||||
| chr5:44303357
|
G | C | 1 | a0001c0001t0064 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1638 | chr5 | 44303357 | |||||
| chr5:44303436
|
G | C | 1 | a0001c0001t0064 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1559C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1559 | chr5 | 44303436 | |||||
| chr5:44303615
|
C | G | 7 | a0001c0001t0001a0001c0001t0013a0001c0001t0017others(4): Show | 62 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1380G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1380 | chr5 | 44303615 | |||||
| chr5:44303658
|
T | C | 53 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(50): Show | 215 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1337A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1337 | chr5 | 44303658 | |||||
| chr5:44303667
|
C | T | 2 | a0001c0001t0008a0001c0001t0051 | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1328 | chr5 | 44303667 | |||||
| chr5:44303715
|
G | C | 1 | a0001c0001t0064 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1280 | chr5 | 44303715 | |||||
| chr5:44303973
|
CT | C | 9 | a0001c0001t0010a0001c0001t0011a0001c0001t0019others(6): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1021delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 1021 | chr5 | 44303973 | |||||
| chr5:44303999
|
A | C | 1 | a0002c0003t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 996 | chr5 | 44303999 | |||||
| chr5:44304014
|
A | G | 1 | a0001c0001t0028 | 2 | NA19043.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*981T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 981 | chr5 | 44304014 | |||||
| chr5:44304151
|
G | A | 1 | a0001c0001t0072 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 844 | chr5 | 44304151 | |||||
| chr5:44304234
|
G | A | 1 | a0001c0001t0067 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 761 | chr5 | 44304234 | |||||
| chr5:44304257
|
C | T | 5 | a0001c0001t0026a0001c0001t0045a0001c0001t0073others(2): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*738G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 738 | chr5 | 44304257 | |||||
| chr5:44304298
|
A | G | 1 | a0001c0001t0049 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 697 | chr5 | 44304298 | |||||
| chr5:44304333
|
C | A | 6 | a0001c0001t0024a0001c0001t0027a0001c0001t0035others(3): Show | 10 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 662 | chr5 | 44304333 | |||||
| chr5:44304618
|
G | A | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(14): Show | 79 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*377C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 377 | chr5 | 44304618 | |||||
| chr5:44304808
|
A | G | 1 | a0001c0001t0048 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 187 | chr5 | 44304808 | |||||
| chr5:44304990
|
T | A | 5 | a0001c0001t0026a0001c0001t0045a0001c0001t0073others(2): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 3/3 | 5 | chr5 | 44304990 | |||||
| chr5:44388715
|
C | T | 3 | a0001c0001t0012a0001c0001t0046a0001c0001t0047 | 8 | HG01106.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-33G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/3 | 33 | chr5 | 44388715 | |||||
| chr5:44388975
|
TC | T | 3 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | 9 | HG01192.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-294delG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/3 | 294 | chr5 | 44388975 | |||||
| chr5:44389322
|
T | C | 1 | a0001c0001t0076 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-640A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/3 | 640 | chr5 | 44389322 | |||||
| chr5:44389366
|
C | G | 4 | a0001c0001t0027a0001c0001t0041a0001c0001t0042others(1): Show | 5 | HG01175.hp2 HG01361.hp1 HG01515.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-684G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/3 | 684 | chr5 | 44389366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44305204
|
A | AAACAGAA others(5): Show |
1 | a0001c0001t0007g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.430-24_430-13dupAA others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305204 | ||||||
| chr5:44305207
|
C | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 62 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.430-15G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305207 | ||||||
| chr5:44305259
|
A | T | 1 | a0001c0001t0017g0316 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.430-67T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305259 | ||||||
| chr5:44305272
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.430-80G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305272 | ||||||
| chr5:44305283
|
TTC | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.430-93_430-92delGA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305283 | ||||||
| chr5:44305413
|
T | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.430-221A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305413 | ||||||
| chr5:44305502
|
A | G | 1 | a0001c0001t0011g0277 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.430-310T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305502 | ||||||
| chr5:44305576
|
G | A | 1 | a0001c0001t0011g0259 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.430-384C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305576 | ||||||
| chr5:44305647
|
A | G | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.430-455T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305647 | ||||||
| chr5:44305654
|
A | G | 3 | a0001c0002t0005g0049a0001c0002t0005g0050a0001c0002t0005g0243 | 3 | HG02258.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430-462T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305654 | ||||||
| chr5:44305748
|
T | C | 115 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(112): Show | 116 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.430-556A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305748 | ||||||
| chr5:44305814
|
G | T | 1 | a0001c0001t0023g0004 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.430-622C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305814 | ||||||
| chr5:44305815
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.430-623G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305815 | ||||||
| chr5:44305858
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.430-666C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305858 | ||||||
| chr5:44305989
|
A | G | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-797T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44305989 | ||||||
| chr5:44306009
|
C | T | 8 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(5): Show | 8 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-817G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306009 | ||||||
| chr5:44306173
|
G | A | 1 | a0001c0001t0023g0116 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.430-981C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306173 | ||||||
| chr5:44306248
|
T | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.430-1056A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306248 | ||||||
| chr5:44306328
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.430-1136G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306328 | ||||||
| chr5:44306390
|
C | T | 3 | a0001c0002t0005g0049a0001c0002t0005g0050a0001c0002t0005g0243 | 3 | HG02258.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430-1198G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306390 | ||||||
| chr5:44306524
|
C | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-1332G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306524 | ||||||
| chr5:44306529
|
GC | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 91 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.430-1338delG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306529 | ||||||
| chr5:44306940
|
T | C | 2 | a0001c0001t0005g0336a0001c0001t0005g0337 | 2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.430-1748A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44306940 | ||||||
| chr5:44307077
|
T | C | 16 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(13): Show | 16 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-1885A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307077 | ||||||
| chr5:44307091
|
C | G | 338 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.430-1899G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307091 | ||||||
| chr5:44307102
|
G | T | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-1910C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307102 | ||||||
| chr5:44307183
|
C | T | 8 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(5): Show | 8 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-1991G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307183 | ||||||
| chr5:44307220
|
G | T | 56 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 60 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.430-2028C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307220 | ||||||
| chr5:44307243
|
C | T | 3 | a0001c0001t0035g0111a0001c0001t0035g0177a0001c0001t0042g0012 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.430-2051G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307243 | ||||||
| chr5:44307409
|
A | C | 1 | a0001c0001t0010g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430-2217T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307409 | ||||||
| chr5:44307474
|
AG | A | 10 | a0001c0001t0018g0103a0001c0001t0018g0105a0001c0001t0018g0106others(7): Show | 11 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-2283delC | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307474 | ||||||
| chr5:44307482
|
A | G | 2 | a0001c0001t0013g0112a0001c0001t0013g0113 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430-2290T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307482 | ||||||
| chr5:44307568
|
G | T | 15 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(12): Show | 15 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.430-2376C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307568 | ||||||
| chr5:44307725
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.430-2533T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307725 | ||||||
| chr5:44307753
|
T | C | 1 | a0001c0001t0045g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430-2561A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307753 | ||||||
| chr5:44307805
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.430-2613A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307805 | ||||||
| chr5:44307820
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.429+2607G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307820 | ||||||
| chr5:44307841
|
A | G | 1 | a0001c0001t0030g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.429+2586T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307841 | ||||||
| chr5:44307873
|
T | C | 1 | a0001c0001t0003g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.429+2554A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307873 | ||||||
| chr5:44307903
|
A | G | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.429+2524T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307903 | ||||||
| chr5:44307939
|
T | A | 1 | a0001c0001t0006g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.429+2488A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44307939 | ||||||
| chr5:44308062
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.429+2365C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308062 | ||||||
| chr5:44308064
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.429+2363T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308064 | ||||||
| chr5:44308150
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.429+2277T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308150 | ||||||
| chr5:44308157
|
A | G | 1 | a0001c0001t0006g0220 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.429+2270T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308157 | ||||||
| chr5:44308283
|
A | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+2144T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308283 | ||||||
| chr5:44308521
|
T | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+1906A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308521 | ||||||
| chr5:44308536
|
G | A | 1 | a0001c0001t0012g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.429+1891C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308536 | ||||||
| chr5:44308796
|
C | A | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+1631G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44308796 | ||||||
| chr5:44309056
|
A | T | 1 | a0001c0001t0063g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.429+1371T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309056 | ||||||
| chr5:44309154
|
G | T | 1 | a0001c0001t0006g0186 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.429+1273C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309154 | ||||||
| chr5:44309582
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.429+845G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309582 | ||||||
| chr5:44309729
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 58 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.429+698G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309729 | ||||||
| chr5:44309797
|
G | T | 1 | a0001c0001t0003g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.429+630C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309797 | ||||||
| chr5:44309837
|
G | T | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0041g0013 | 3 | HG01361.hp1 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.429+590C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44309837 | ||||||
| chr5:44310203
|
GC | G | 9 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 9 | HG01943.hp2 HG02293.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+223delG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44310203 | ||||||
| chr5:44310230
|
A | T | 1 | a0001c0001t0012g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429+197T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44310230 | ||||||
| chr5:44310276
|
C | T | 1 | a0001c0001t0005g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.429+151G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44310276 | ||||||
| chr5:44310390
|
A | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 81 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+37T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 2/2 | chr5 | 44310390 | ||||||
| chr5:44310559
|
T | C | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0022g0242others(1): Show | 4 | HG01361.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-29A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44310559 | ||||||
| chr5:44310718
|
C | A | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-188G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44310718 | ||||||
| chr5:44310910
|
G | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-380C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44310910 | ||||||
| chr5:44310968
|
A | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 92 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.326-438T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44310968 | ||||||
| chr5:44311337
|
A | C | 338 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.326-807T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311337 | ||||||
| chr5:44311383
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.326-853G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311383 | ||||||
| chr5:44311433
|
C | A | 1 | a0001c0001t0003g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326-903G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311433 | ||||||
| chr5:44311666
|
C | T | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 107 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.326-1136G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311666 | ||||||
| chr5:44311757
|
C | A | 1 | a0001c0001t0015g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.326-1227G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311757 | ||||||
| chr5:44311764
|
C | T | 2 | a0001c0001t0018g0114a0001c0001t0023g0116 | 2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.326-1234G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311764 | ||||||
| chr5:44311830
|
A | C | 1 | a0001c0001t0075g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.326-1300T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44311830 | ||||||
| chr5:44312019
|
C | T | 1 | a0001c0001t0003g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326-1489G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312019 | ||||||
| chr5:44312121
|
A | T | 1 | a0001c0001t0019g0254 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.326-1591T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312121 | ||||||
| chr5:44312141
|
C | T | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-1611G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312141 | ||||||
| chr5:44312195
|
T | TAC | 127 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(124): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.326-1667_326-1666d others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312195 | ||||||
| chr5:44312195
|
T | TACAC | 4 | a0001c0001t0002g0172a0001c0001t0006g0205a0001c0001t0029g0135others(1): Show | 4 | HG01952.hp1 HG02293.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-1669_326-1666d others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312195 | ||||||
| chr5:44312195
|
TAC | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 168 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.326-1667_326-1666d others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312195 | ||||||
| chr5:44312201
|
C | T | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-1671G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312201 | ||||||
| chr5:44312288
|
T | C | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326-1758A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312288 | ||||||
| chr5:44312314
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.326-1784C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312314 | ||||||
| chr5:44312374
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.326-1844T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312374 | ||||||
| chr5:44312387
|
A | G | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-1857T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312387 | ||||||
| chr5:44312582
|
G | A | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.326-2052C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312582 | ||||||
| chr5:44312660
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-2130C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312660 | ||||||
| chr5:44312802
|
G | A | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-2272C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312802 | ||||||
| chr5:44312810
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.326-2280A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312810 | ||||||
| chr5:44312842
|
G | T | 1 | a0001c0001t0021g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.326-2312C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312842 | ||||||
| chr5:44312921
|
C | T | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-2391G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44312921 | ||||||
| chr5:44313049
|
C | T | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-2519G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313049 | ||||||
| chr5:44313116
|
T | C | 1 | a0001c0001t0062g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-2586A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313116 | ||||||
| chr5:44313180
|
G | T | 205 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(202): Show | 213 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.326-2650C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313180 | ||||||
| chr5:44313201
|
T | C | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-2671A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313201 | ||||||
| chr5:44313429
|
T | C | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0022g0242others(1): Show | 4 | HG01361.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-2899A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313429 | ||||||
| chr5:44313521
|
A | G | 76 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(73): Show | 77 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.326-2991T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313521 | ||||||
| chr5:44313548
|
G | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 81 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.326-3018C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313548 | ||||||
| chr5:44313588
|
G | GT | 122 | a0001c0001t0001g0330a0001c0001t0001g0332a0001c0001t0002g0031others(119): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.326-3059dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313588 | ||||||
| chr5:44313588
|
G | GTT | 9 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0134others(6): Show | 9 | HG00733.hp1 HG01069.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-3060_326-3059d others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313588 | ||||||
| chr5:44313588
|
GT | G | 78 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.326-3059delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313588 | ||||||
| chr5:44313590
|
T | TG | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.326-3061_326-3060i others(3): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313590 | ||||||
| chr5:44313591
|
T | G | 1 | a0001c0001t0010g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.326-3061A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313591 | ||||||
| chr5:44313965
|
C | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-3435G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313965 | ||||||
| chr5:44314147
|
C | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-3617G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314147 | ||||||
| chr5:44314193
|
G | T | 1 | a0001c0001t0014g0066 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.326-3663C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314193 | ||||||
| chr5:44314506
|
T | G | 1 | a0001c0001t0010g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.326-3976A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314506 | ||||||
| chr5:44314512
|
T | C | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-3982A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314512 | ||||||
| chr5:44314530
|
CATCACCT others(5): Show |
C | 10 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0282others(7): Show | 10 | HG02145.hp1 HG02723.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.326-4012_326-4001d others(14): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314530 | ||||||
| chr5:44314605
|
G | A | 1 | a0001c0001t0006g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.326-4075C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314605 | ||||||
| chr5:44314681
|
T | C | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-4151A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314681 | ||||||
| chr5:44314789
|
G | A | 2 | a0001c0001t0005g0093a0001c0001t0072g0340 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.326-4259C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44314789 | ||||||
| chr5:44315006
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 92 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.326-4476A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315006 | ||||||
| chr5:44315009
|
A | G | 1 | a0001c0001t0071g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.326-4479T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315009 | ||||||
| chr5:44315054
|
T | G | 2 | a0001c0001t0009g0020a0001c0001t0009g0022 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.326-4524A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315054 | ||||||
| chr5:44315147
|
C | T | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-4617G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315147 | ||||||
| chr5:44315182
|
CA | C | 150 | a0001c0001t0001g0286a0001c0001t0001g0298a0001c0001t0001g0299others(147): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.326-4653delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315182 | ||||||
| chr5:44315182
|
CAA | C | 120 | a0001c0001t0002g0133a0001c0001t0003g0108a0001c0001t0004g0033others(117): Show | 122 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.326-4654_326-4653d others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315182 | ||||||
| chr5:44315182
|
CAAA | C | 9 | a0001c0001t0004g0285a0001c0001t0022g0182a0001c0001t0026g0247others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.326-4655_326-4653d others(5): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315182 | ||||||
| chr5:44315196
|
A | T | 1 | a0001c0001t0003g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326-4666T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315196 | ||||||
| chr5:44315272
|
C | T | 7 | a0001c0001t0024g0121a0001c0001t0024g0338a0001c0001t0024g0339others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-4742G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315272 | ||||||
| chr5:44315514
|
G | A | 4 | a0001c0001t0018g0103a0001c0001t0018g0105a0001c0001t0018g0106others(1): Show | 4 | HG01192.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-4984C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315514 | ||||||
| chr5:44315641
|
T | C | 338 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.326-5111A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315641 | ||||||
| chr5:44315705
|
C | A | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-5175G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315705 | ||||||
| chr5:44315730
|
C | A | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-5200G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315730 | ||||||
| chr5:44315741
|
G | T | 1 | a0001c0002t0005g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.326-5211C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315741 | ||||||
| chr5:44315765
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.326-5235T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315765 | ||||||
| chr5:44315832
|
G | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-5302C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315832 | ||||||
| chr5:44315921
|
G | A | 2 | a0001c0001t0017g0295a0001c0001t0017g0296 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.326-5391C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315921 | ||||||
| chr5:44315936
|
T | C | 1 | a0001c0001t0015g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.326-5406A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315936 | ||||||
| chr5:44316225
|
C | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.326-5695G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316225 | ||||||
| chr5:44316333
|
G | A | 1 | a0001c0001t0010g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.326-5803C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316333 | ||||||
| chr5:44316336
|
T | A | 1 | a0001c0001t0002g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.326-5806A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316336 | ||||||
| chr5:44316402
|
C | A | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-5872G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316402 | ||||||
| chr5:44316536
|
G | A | 1 | a0001c0001t0027g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.326-6006C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316536 | ||||||
| chr5:44316700
|
T | G | 1 | a0001c0001t0001g0293 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.326-6170A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316700 | ||||||
| chr5:44316765
|
A | C | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.326-6235T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316765 | ||||||
| chr5:44316813
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326-6283A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316813 | ||||||
| chr5:44316989
|
G | A | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-6459C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316989 | ||||||
| chr5:44316994
|
G | C | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-6464C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44316994 | ||||||
| chr5:44317080
|
G | T | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-6550C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317080 | ||||||
| chr5:44317106
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.326-6576T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317106 | ||||||
| chr5:44317815
|
T | C | 6 | a0001c0001t0002g0156a0001c0001t0002g0188a0001c0001t0003g0149others(3): Show | 6 | NA18940.hp1 NA18965.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-7285A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317815 | ||||||
| chr5:44317889
|
C | T | 3 | a0001c0001t0028g0249a0001c0001t0028g0250a0001c0001t0060g0219 | 3 | HG02818.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-7359G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317889 | ||||||
| chr5:44317940
|
G | A | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.326-7410C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317940 | ||||||
| chr5:44317984
|
G | A | 5 | a0001c0001t0012g0001a0001c0001t0012g0025a0001c0001t0012g0026others(2): Show | 6 | HG01106.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.326-7454C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44317984 | ||||||
| chr5:44318015
|
A | G | 26 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(23): Show | 26 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.326-7485T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318015 | ||||||
| chr5:44318035
|
T | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-7505A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318035 | ||||||
| chr5:44318123
|
C | A | 1 | a0001c0001t0018g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.326-7593G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318123 | ||||||
| chr5:44318242
|
T | C | 2 | a0001c0001t0029g0135a0001c0001t0029g0139 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.326-7712A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318242 | ||||||
| chr5:44318341
|
T | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-7811A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318341 | ||||||
| chr5:44318430
|
C | A | 185 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(182): Show | 192 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.326-7900G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318430 | ||||||
| chr5:44318522
|
A | G | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-7992T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318522 | ||||||
| chr5:44318616
|
A | T | 16 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(13): Show | 16 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.326-8086T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318616 | ||||||
| chr5:44318782
|
C | G | 3 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0073g0279 | 3 | HG02109.hp1 HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.326-8252G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44318782 | ||||||
| chr5:44319034
|
G | T | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-8504C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319034 | ||||||
| chr5:44319228
|
T | A | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-8698A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319228 | ||||||
| chr5:44319244
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.326-8714C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319244 | ||||||
| chr5:44319248
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0179 | 3 | HG01069.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.326-8718C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319248 | ||||||
| chr5:44319317
|
T | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-8787A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319317 | ||||||
| chr5:44319388
|
A | C | 1 | a0001c0001t0039g0222 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.326-8858T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319388 | ||||||
| chr5:44319430
|
C | T | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.326-8900G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319430 | ||||||
| chr5:44319637
|
A | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-9107T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319637 | ||||||
| chr5:44319787
|
A | G | 2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | NA18943.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.326-9257T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319787 | ||||||
| chr5:44319876
|
C | T | 1 | a0001c0001t0003g0201 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.326-9346G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44319876 | ||||||
| chr5:44320022
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0006g0155 | 2 | HG00597.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.326-9492A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320022 | ||||||
| chr5:44320039
|
C | G | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-9509G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320039 | ||||||
| chr5:44320042
|
G | A | 1 | a0001c0001t0005g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326-9512C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320042 | ||||||
| chr5:44320045
|
C | A | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-9515G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320045 | ||||||
| chr5:44320095
|
C | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-9565G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320095 | ||||||
| chr5:44320157
|
T | C | 2 | a0001c0001t0017g0295a0001c0001t0017g0296 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.326-9627A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320157 | ||||||
| chr5:44320417
|
T | C | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-9887A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320417 | ||||||
| chr5:44320552
|
G | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-10022C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320552 | ||||||
| chr5:44320712
|
CT | C | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-10183delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320712 | ||||||
| chr5:44320866
|
C | T | 77 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(74): Show | 78 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.326-10336G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320866 | ||||||
| chr5:44320867
|
G | A | 33 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.326-10337C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320867 | ||||||
| chr5:44321003
|
GA | G | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-10474delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321003 | ||||||
| chr5:44321058
|
C | T | 5 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0305others(2): Show | 5 | HG00544.hp1 HG02165.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.326-10528G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321058 | ||||||
| chr5:44321098
|
T | C | 76 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(73): Show | 77 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.326-10568A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321098 | ||||||
| chr5:44321166
|
A | T | 1 | a0001c0001t0058g0317 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.326-10636T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321166 | ||||||
| chr5:44321219
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-10689G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321219 | ||||||
| chr5:44321450
|
A | G | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-10920T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321450 | ||||||
| chr5:44321534
|
G | A | 76 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0004g0033others(73): Show | 77 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.326-11004C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321534 | ||||||
| chr5:44321594
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.326-11064C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321594 | ||||||
| chr5:44321614
|
A | G | 9 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(6): Show | 9 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-11084T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321614 | ||||||
| chr5:44321841
|
A | G | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-11311T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44321841 | ||||||
| chr5:44322009
|
C | T | 26 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(23): Show | 26 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.326-11479G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322009 | ||||||
| chr5:44322031
|
G | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.326-11501C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322031 | ||||||
| chr5:44322055
|
G | A | 2 | a0001c0001t0008g0096a0001c0001t0008g0101 | 2 | HG01123.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.326-11525C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322055 | ||||||
| chr5:44322109
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.326-11579A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322109 | ||||||
| chr5:44322208
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 65 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.326-11678T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322208 | ||||||
| chr5:44322276
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-11746C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322276 | ||||||
| chr5:44322457
|
G | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-11927C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322457 | ||||||
| chr5:44322525
|
C | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-11995G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322525 | ||||||
| chr5:44322548
|
G | A | 1 | a0001c0001t0018g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.326-12018C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322548 | ||||||
| chr5:44322739
|
C | G | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-12209G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322739 | ||||||
| chr5:44322768
|
T | C | 2 | a0001c0001t0013g0112a0001c0001t0013g0113 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.326-12238A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322768 | ||||||
| chr5:44322865
|
A | T | 2 | a0001c0001t0005g0039a0001c0001t0005g0055 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.326-12335T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322865 | ||||||
| chr5:44322912
|
C | T | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-12382G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44322912 | ||||||
| chr5:44323071
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.326-12541C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323071 | ||||||
| chr5:44323143
|
C | T | 3 | a0001c0001t0007g0069a0001c0001t0007g0071a0001c0001t0007g0081 | 3 | NA18962.hp1 NA19074.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.326-12613G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323143 | ||||||
| chr5:44323276
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.326-12746T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323276 | ||||||
| chr5:44323358
|
G | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-12828C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323358 | ||||||
| chr5:44323616
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-13086C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323616 | ||||||
| chr5:44323647
|
C | G | 2 | a0001c0001t0004g0059a0001c0001t0007g0042 | 2 | HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.326-13117G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323647 | ||||||
| chr5:44323799
|
T | C | 1 | a0001c0001t0001g0009 | 2 | NA19007.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.326-13269A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44323799 | ||||||
| chr5:44324139
|
G | C | 16 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(13): Show | 16 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.326-13609C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44324139 | ||||||
| chr5:44324336
|
C | T | 1 | a0001c0001t0004g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.326-13806G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44324336 | ||||||
| chr5:44324455
|
A | G | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-13925T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44324455 | ||||||
| chr5:44324610
|
T | A | 1 | a0001c0001t0033g0257 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.326-14080A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44324610 | ||||||
| chr5:44325075
|
C | T | 2 | a0001c0001t0005g0044a0001c0001t0005g0045 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.326-14545G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325075 | ||||||
| chr5:44325220
|
A | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(108): Show | 117 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.326-14690T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325220 | ||||||
| chr5:44325367
|
T | C | 129 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(126): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.326-14837A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325367 | ||||||
| chr5:44325405
|
C | A | 185 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(182): Show | 192 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.326-14875G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325405 | ||||||
| chr5:44325435
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 65 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.326-14905G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325435 | ||||||
| chr5:44325505
|
A | G | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-14975T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325505 | ||||||
| chr5:44325611
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-15081G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325611 | ||||||
| chr5:44325643
|
C | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-15113G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325643 | ||||||
| chr5:44325799
|
C | A | 1 | a0001c0001t0061g0115 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.326-15269G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325799 | ||||||
| chr5:44325881
|
TA | T | 193 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 200 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.326-15352delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325881 | ||||||
| chr5:44325946
|
C | T | 1 | a0001c0001t0013g0300 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.326-15416G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325946 | ||||||
| chr5:44326185
|
T | C | 10 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(7): Show | 11 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.326-15655A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326185 | ||||||
| chr5:44326273
|
T | C | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-15743A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326273 | ||||||
| chr5:44326315
|
G | C | 1 | a0001c0001t0061g0115 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.326-15785C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326315 | ||||||
| chr5:44326502
|
G | A | 103 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(100): Show | 104 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.326-15972C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326502 | ||||||
| chr5:44326523
|
C | T | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-15993G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326523 | ||||||
| chr5:44326896
|
G | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 65 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.326-16366C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44326896 | ||||||
| chr5:44327144
|
A | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-16614T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327144 | ||||||
| chr5:44327172
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.326-16642G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327172 | ||||||
| chr5:44327268
|
A | G | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-16738T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327268 | ||||||
| chr5:44327307
|
G | T | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.326-16777C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327307 | ||||||
| chr5:44327329
|
C | T | 14 | a0001c0001t0004g0033a0001c0001t0004g0064a0001c0001t0004g0065others(11): Show | 14 | HG00438.hp1 HG02056.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.326-16799G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327329 | ||||||
| chr5:44327506
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.326-16976G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327506 | ||||||
| chr5:44327762
|
T | C | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-17232A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327762 | ||||||
| chr5:44327764
|
T | C | 1 | a0001c0001t0001g0333 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.326-17234A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327764 | ||||||
| chr5:44327787
|
C | T | 9 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(6): Show | 9 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-17257G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44327787 | ||||||
| chr5:44328003
|
G | A | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-17473C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328003 | ||||||
| chr5:44328108
|
T | C | 6 | a0001c0001t0004g0043a0001c0001t0004g0051a0001c0001t0004g0059others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-17578A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328108 | ||||||
| chr5:44328147
|
A | G | 332 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(329): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-17617T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328147 | ||||||
| chr5:44328168
|
T | C | 147 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.326-17638A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328168 | ||||||
| chr5:44328181
|
T | C | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.326-17651A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328181 | ||||||
| chr5:44328223
|
T | C | 147 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.326-17693A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328223 | ||||||
| chr5:44328344
|
T | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18966.hp2 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.326-17814A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328344 | ||||||
| chr5:44328451
|
C | A | 332 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(329): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-17921G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328451 | ||||||
| chr5:44328464
|
A | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0179 | 3 | HG01069.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.326-17934T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328464 | ||||||
| chr5:44328480
|
G | A | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-17950C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328480 | ||||||
| chr5:44328525
|
A | G | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-17995T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328525 | ||||||
| chr5:44328629
|
A | G | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.326-18099T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328629 | ||||||
| chr5:44328679
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0006g0227 | 2 | NA18965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.326-18149A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328679 | ||||||
| chr5:44328720
|
T | A | 2 | a0001c0001t0005g0044a0001c0001t0005g0045 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.326-18190A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328720 | ||||||
| chr5:44328727
|
A | C | 147 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.326-18197T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328727 | ||||||
| chr5:44328755
|
G | A | 2 | a0001c0001t0011g0277a0001c0001t0019g0261 | 2 | NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.326-18225C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328755 | ||||||
| chr5:44328866
|
C | T | 1 | a0001c0001t0029g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326-18336G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328866 | ||||||
| chr5:44328954
|
A | G | 325 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.326-18424T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328954 | ||||||
| chr5:44329081
|
G | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-18551C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329081 | ||||||
| chr5:44329101
|
G | A | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-18571C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329101 | ||||||
| chr5:44329133
|
G | A | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.326-18603C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329133 | ||||||
| chr5:44329330
|
C | T | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.326-18800G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329330 | ||||||
| chr5:44329340
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.326-18810G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329340 | ||||||
| chr5:44329363
|
C | T | 1 | a0001c0001t0004g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.326-18833G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329363 | ||||||
| chr5:44329376
|
C | A | 1 | a0001c0001t0018g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.326-18846G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329376 | ||||||
| chr5:44329387
|
G | C | 6 | a0001c0002t0005g0049a0001c0002t0005g0050a0001c0002t0005g0052others(3): Show | 6 | HG01167.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-18857C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329387 | ||||||
| chr5:44329527
|
T | G | 1 | a0001c0001t0023g0004 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.326-18997A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329527 | ||||||
| chr5:44329759
|
T | G | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0080others(2): Show | 5 | NA18953.hp2 NA18971.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.326-19229A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329759 | ||||||
| chr5:44329790
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-19260G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44329790 | ||||||
| chr5:44330057
|
G | C | 1 | a0001c0001t0011g0262 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.326-19527C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330057 | ||||||
| chr5:44330170
|
G | A | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326-19640C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330170 | ||||||
| chr5:44330462
|
C | T | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-19932G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330462 | ||||||
| chr5:44330729
|
G | A | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-20199C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330729 | ||||||
| chr5:44330755
|
C | T | 51 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(48): Show | 51 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.326-20225G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330755 | ||||||
| chr5:44330787
|
C | T | 13 | a0001c0001t0005g0039a0001c0001t0005g0041a0001c0001t0005g0044others(10): Show | 14 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.326-20257G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330787 | ||||||
| chr5:44330811
|
A | G | 1 | a0001c0001t0024g0121 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326-20281T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330811 | ||||||
| chr5:44330893
|
A | G | 147 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.326-20363T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330893 | ||||||
| chr5:44330944
|
C | A | 2 | a0001c0001t0034g0274a0001c0001t0034g0275 | 2 | NA18950.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.326-20414G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330944 | ||||||
| chr5:44331378
|
A | G | 1 | a0001c0001t0076g0341 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.326-20848T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331378 | ||||||
| chr5:44331435
|
A | G | 13 | a0001c0001t0004g0033a0001c0001t0004g0064a0001c0001t0004g0065others(10): Show | 13 | HG00438.hp1 HG02056.hp2 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.326-20905T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331435 | ||||||
| chr5:44331493
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.326-20963G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331493 | ||||||
| chr5:44331630
|
G | A | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-21100C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331630 | ||||||
| chr5:44331649
|
T | A | 147 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.326-21119A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331649 | ||||||
| chr5:44331689
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.326-21159C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331689 | ||||||
| chr5:44331765
|
T | C | 7 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-21235A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331765 | ||||||
| chr5:44331789
|
T | C | 1 | a0001c0001t0003g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.326-21259A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331789 | ||||||
| chr5:44331803
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-21273G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331803 | ||||||
| chr5:44331890
|
T | C | 1 | a0001c0001t0013g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.326-21360A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331890 | ||||||
| chr5:44331993
|
C | A | 1 | a0001c0001t0005g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.326-21463G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44331993 | ||||||
| chr5:44332098
|
A | C | 1 | a0001c0001t0010g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.326-21568T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332098 | ||||||
| chr5:44332154
|
G | C | 2 | a0001c0001t0029g0135a0001c0001t0029g0139 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.326-21624C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332154 | ||||||
| chr5:44332192
|
G | A | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326-21662C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332192 | ||||||
| chr5:44332296
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326-21766A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332296 | ||||||
| chr5:44332319
|
C | A | 1 | a0001c0001t0003g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.326-21789G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332319 | ||||||
| chr5:44332372
|
A | G | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.326-21842T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332372 | ||||||
| chr5:44332415
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.326-21885A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332415 | ||||||
| chr5:44332490
|
A | C | 1 | a0001c0001t0010g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.326-21960T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332490 | ||||||
| chr5:44332669
|
C | T | 1 | a0001c0001t0022g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.326-22139G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332669 | ||||||
| chr5:44332867
|
G | C | 1 | a0001c0001t0062g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-22337C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332867 | ||||||
| chr5:44332901
|
C | T | 3 | a0001c0001t0005g0290a0001c0001t0005g0336a0001c0001t0005g0337 | 3 | HG02738.hp2 HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.326-22371G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332901 | ||||||
| chr5:44332920
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.326-22390C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44332920 | ||||||
| chr5:44333103
|
C | T | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-22573G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333103 | ||||||
| chr5:44333110
|
C | A | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.326-22580G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333110 | ||||||
| chr5:44333189
|
C | G | 1 | a0001c0001t0002g0165 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.326-22659G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333189 | ||||||
| chr5:44333353
|
A | G | 1 | a0001c0001t0024g0121 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326-22823T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333353 | ||||||
| chr5:44333789
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.326-23259A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333789 | ||||||
| chr5:44333870
|
G | A | 1 | a0001c0001t0008g0100 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.326-23340C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333870 | ||||||
| chr5:44333890
|
C | G | 11 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(8): Show | 11 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.326-23360G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333890 | ||||||
| chr5:44333949
|
A | G | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 77 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.326-23419T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44333949 | ||||||
| chr5:44334022
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.326-23492G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334022 | ||||||
| chr5:44334093
|
A | G | 1 | a0001c0001t0003g0153 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.326-23563T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334093 | ||||||
| chr5:44334209
|
G | C | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326-23679C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334209 | ||||||
| chr5:44334308
|
C | T | 2 | a0001c0001t0007g0090a0001c0001t0007g0091 | 2 | NA18951.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.326-23778G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334308 | ||||||
| chr5:44334400
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.326-23870T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334400 | ||||||
| chr5:44334483
|
C | T | 9 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0282others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-23953G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334483 | ||||||
| chr5:44334707
|
T | C | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-24177A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334707 | ||||||
| chr5:44334840
|
C | G | 2 | a0001c0001t0019g0263a0001c0001t0019g0268 | 2 | NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.326-24310G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334840 | ||||||
| chr5:44334881
|
A | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-24351T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334881 | ||||||
| chr5:44334910
|
C | G | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG01975.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.326-24380G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334910 | ||||||
| chr5:44334912
|
G | A | 33 | a0001c0001t0004g0033a0001c0001t0004g0064a0001c0001t0004g0065others(30): Show | 33 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.326-24382C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334912 | ||||||
| chr5:44334944
|
T | G | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-24414A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334944 | ||||||
| chr5:44334983
|
T | A | 1 | a0001c0001t0006g0124 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.326-24453A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334983 | ||||||
| chr5:44334983
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.326-24453A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334983 | ||||||
| chr5:44335225
|
C | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-24695G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335225 | ||||||
| chr5:44335236
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-24706C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335236 | ||||||
| chr5:44335310
|
T | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-24780A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335310 | ||||||
| chr5:44335314
|
C | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-24784G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335314 | ||||||
| chr5:44335421
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.326-24891G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335421 | ||||||
| chr5:44335421
|
C | CA | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-24892dupT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335421 | ||||||
| chr5:44335623
|
A | G | 1 | a0001c0001t0037g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.326-25093T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335623 | ||||||
| chr5:44335685
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.326-25155T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335685 | ||||||
| chr5:44335718
|
T | C | 133 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(130): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.326-25188A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335718 | ||||||
| chr5:44335819
|
T | C | 1 | a0003c0004t0038g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.326-25289A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335819 | ||||||
| chr5:44335829
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.326-25299T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335829 | ||||||
| chr5:44335839
|
A | G | 4 | a0001c0001t0018g0103a0001c0001t0018g0105a0001c0001t0018g0106others(1): Show | 4 | HG01192.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-25309T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335839 | ||||||
| chr5:44335885
|
G | C | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326-25355C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335885 | ||||||
| chr5:44335925
|
C | A | 12 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0009g0015others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.326-25395G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44335925 | ||||||
| chr5:44336209
|
T | C | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-25679A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336209 | ||||||
| chr5:44336251
|
A | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-25721T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336251 | ||||||
| chr5:44336514
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-25984C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336514 | ||||||
| chr5:44336661
|
C | T | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-26131G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336661 | ||||||
| chr5:44336771
|
A | C | 1 | a0001c0001t0043g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.326-26241T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336771 | ||||||
| chr5:44336848
|
C | T | 1 | a0001c0001t0025g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.326-26318G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336848 | ||||||
| chr5:44336902
|
G | A | 2 | a0001c0001t0035g0111a0001c0001t0035g0177 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.326-26372C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336902 | ||||||
| chr5:44336988
|
A | G | 1 | a0001c0001t0037g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.326-26458T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44336988 | ||||||
| chr5:44337111
|
G | T | 4 | a0001c0001t0003g0108a0001c0001t0018g0109a0001c0001t0023g0004others(1): Show | 5 | HG01515.hp2 HG01517.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.326-26581C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337111 | ||||||
| chr5:44337134
|
A | AT | 19 | a0001c0001t0002g0204a0001c0001t0008g0003a0001c0001t0008g0095others(16): Show | 20 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.326-26605dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337134 | ||||||
| chr5:44337134
|
A | ATT | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 76 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.326-26606_326-2660 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337134 | ||||||
| chr5:44337262
|
TA | T | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-26733delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337262 | ||||||
| chr5:44337378
|
G | A | 340 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(337): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.326-26848C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337378 | ||||||
| chr5:44337536
|
A | C | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-27006T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337536 | ||||||
| chr5:44337588
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-27058G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337588 | ||||||
| chr5:44337680
|
G | A | 1 | a0001c0001t0017g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.326-27150C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337680 | ||||||
| chr5:44337724
|
G | A | 10 | a0001c0001t0005g0237a0001c0001t0026g0247a0001c0001t0026g0248others(7): Show | 10 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.326-27194C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337724 | ||||||
| chr5:44337768
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.326-27238G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337768 | ||||||
| chr5:44337770
|
T | C | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.326-27240A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337770 | ||||||
| chr5:44337802
|
G | T | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.326-27272C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337802 | ||||||
| chr5:44337918
|
C | T | 2 | a0001c0001t0006g0185a0001c0001t0006g0186 | 2 | NA18995.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.326-27388G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337918 | ||||||
| chr5:44337926
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-27396G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337926 | ||||||
| chr5:44338213
|
G | A | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-27683C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338213 | ||||||
| chr5:44338220
|
C | T | 19 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(16): Show | 19 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.326-27690G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338220 | ||||||
| chr5:44338325
|
A | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-27795T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338325 | ||||||
| chr5:44338544
|
G | A | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-28014C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338544 | ||||||
| chr5:44338611
|
T | A | 1 | a0001c0001t0005g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.326-28081A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338611 | ||||||
| chr5:44338657
|
C | T | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.326-28127G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338657 | ||||||
| chr5:44338734
|
A | G | 8 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-28204T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338734 | ||||||
| chr5:44338837
|
G | A | 29 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(26): Show | 29 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.326-28307C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44338837 | ||||||
| chr5:44339073
|
G | A | 12 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0009g0015others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.326-28543C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339073 | ||||||
| chr5:44339080
|
G | A | 1 | a0001c0001t0065g0264 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.326-28550C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339080 | ||||||
| chr5:44339129
|
A | G | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-28599T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339129 | ||||||
| chr5:44339327
|
T | C | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-28797A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339327 | ||||||
| chr5:44339662
|
T | G | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-29132A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339662 | ||||||
| chr5:44339683
|
T | C | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-29153A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339683 | ||||||
| chr5:44339708
|
G | A | 131 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(128): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.326-29178C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339708 | ||||||
| chr5:44339882
|
G | A | 130 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(127): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.326-29352C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339882 | ||||||
| chr5:44340050
|
A | C | 3 | a0001c0001t0003g0005a0001c0001t0003g0148a0001c0001t0003g0194 | 4 | NA19009.hp2 NA19066.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-29520T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340050 | ||||||
| chr5:44340096
|
C | T | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-29566G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340096 | ||||||
| chr5:44340098
|
C | G | 129 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(126): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.326-29568G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340098 | ||||||
| chr5:44340119
|
A | G | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-29589T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340119 | ||||||
| chr5:44340134
|
G | A | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326-29604C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340134 | ||||||
| chr5:44340159
|
A | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-29629T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340159 | ||||||
| chr5:44340217
|
A | G | 6 | a0001c0001t0018g0103a0001c0001t0018g0105a0001c0001t0018g0106others(3): Show | 6 | HG01192.hp2 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.326-29687T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340217 | ||||||
| chr5:44340233
|
G | T | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.326-29703C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340233 | ||||||
| chr5:44340435
|
G | T | 6 | a0001c0002t0005g0049a0001c0002t0005g0050a0001c0002t0005g0052others(3): Show | 6 | HG01167.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-29905C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340435 | ||||||
| chr5:44340633
|
C | T | 1 | a0001c0001t0004g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.326-30103G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340633 | ||||||
| chr5:44340796
|
G | T | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-30266C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340796 | ||||||
| chr5:44340825
|
T | C | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.326-30295A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340825 | ||||||
| chr5:44340873
|
T | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-30343A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340873 | ||||||
| chr5:44340936
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.326-30406C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340936 | ||||||
| chr5:44341023
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-30493A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341023 | ||||||
| chr5:44341105
|
C | T | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-30575G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341105 | ||||||
| chr5:44341234
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-30704T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341234 | ||||||
| chr5:44341282
|
C | T | 1 | a0001c0001t0045g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.326-30752G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341282 | ||||||
| chr5:44341331
|
A | G | 1 | a0001c0001t0002g0328 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.326-30801T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341331 | ||||||
| chr5:44341349
|
C | A | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-30819G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341349 | ||||||
| chr5:44341494
|
TA | T | 75 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(72): Show | 76 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.326-30965delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341494 | ||||||
| chr5:44341531
|
A | G | 1 | a0001c0001t0007g0291 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.326-31001T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341531 | ||||||
| chr5:44341532
|
G | A | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-31002C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341532 | ||||||
| chr5:44341598
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.326-31068G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341598 | ||||||
| chr5:44341630
|
GATTTAAC others(7): Show |
G | 1 | a0001c0001t0003g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326-31114_326-3110 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341630 | ||||||
| chr5:44341700
|
G | A | 1 | a0001c0001t0030g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.326-31170C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341700 | ||||||
| chr5:44341703
|
C | T | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.326-31173G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341703 | ||||||
| chr5:44341719
|
A | C | 1 | a0001c0001t0062g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-31189T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341719 | ||||||
| chr5:44341781
|
G | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.326-31251C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341781 | ||||||
| chr5:44341823
|
C | G | 3 | a0001c0001t0003g0005a0001c0001t0003g0148a0001c0001t0003g0194 | 4 | NA19009.hp2 NA19066.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-31293G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341823 | ||||||
| chr5:44341877
|
A | G | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.326-31347T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341877 | ||||||
| chr5:44342070
|
A | G | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-31540T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342070 | ||||||
| chr5:44342198
|
G | A | 1 | a0001c0001t0010g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.326-31668C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342198 | ||||||
| chr5:44342512
|
GA | G | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 131 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.326-31983delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342512 | ||||||
| chr5:44342622
|
C | A | 1 | a0001c0001t0001g0325 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.326-32092G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342622 | ||||||
| chr5:44342772
|
C | T | 1 | a0001c0001t0037g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.326-32242G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342772 | ||||||
| chr5:44342923
|
C | T | 9 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(6): Show | 9 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-32393G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342923 | ||||||
| chr5:44342938
|
T | A | 1 | a0001c0001t0002g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.326-32408A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44342938 | ||||||
| chr5:44343045
|
T | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-32515A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343045 | ||||||
| chr5:44343375
|
T | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-32845A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343375 | ||||||
| chr5:44343391
|
C | T | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-32861G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343391 | ||||||
| chr5:44343504
|
T | TAC | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.326-32975_326-3297 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343504 | ||||||
| chr5:44343529
|
C | T | 2 | a0001c0001t0029g0135a0001c0001t0029g0139 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.326-32999G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343529 | ||||||
| chr5:44343705
|
T | C | 2 | a0001c0001t0017g0295a0001c0001t0017g0296 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.326-33175A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44343705 | ||||||
| chr5:44344116
|
A | G | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(4): Show | 7 | NA18965.hp2 NA18974.hp1 NA19012.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-33586T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344116 | ||||||
| chr5:44344225
|
T | C | 1 | a0001c0001t0062g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-33695A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344225 | ||||||
| chr5:44344231
|
T | A | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.326-33701A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344231 | ||||||
| chr5:44344276
|
TATGGATT others(632): Show |
T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-34385_326-3374 others(4): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344276 | ||||||
| chr5:44344325
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.326-33795A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344325 | ||||||
| chr5:44344513
|
AG | A | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-33984delC | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344513 | ||||||
| chr5:44344568
|
C | CTCTCTGT others(11): Show |
1 | a0001c0001t0009g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.326-34039_326-3403 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTCTGTGT others(5): Show |
1 | a0001c0001t0003g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.326-34039_326-3403 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTCTGTGT others(7): Show |
10 | a0001c0001t0003g0229a0001c0001t0009g0015a0001c0001t0009g0017others(7): Show | 10 | HG01169.hp1 HG01192.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.326-34039_326-3403 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTCTGTGT others(9): Show |
2 | a0001c0001t0004g0057a0001c0001t0052g0123 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.326-34039_326-3403 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTCTGTGT others(11): Show |
1 | a0001c0001t0002g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.326-34039_326-3403 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTG | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 58 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.326-34042_326-3403 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTG | 13 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(10): Show | 13 | HG00733.hp2 HG02647.hp2 NA18961.hp1 others(10): Show |
intron_variant | MODIFIER | c.326-34044_326-3403 others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(1): Show |
20 | a0001c0001t0001g0179a0001c0001t0001g0286a0001c0001t0001g0299others(17): Show | 21 | HG00280.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.326-34046_326-3403 others(12): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(3): Show |
20 | a0001c0001t0002g0156a0001c0001t0004g0074a0001c0001t0004g0075others(17): Show | 20 | HG00621.hp2 HG01261.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.326-34048_326-3403 others(14): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(5): Show |
44 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(41): Show | 45 | HG00438.hp1 HG00673.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.326-34050_326-3403 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(7): Show |
44 | a0001c0001t0002g0134a0001c0001t0002g0143a0001c0001t0002g0188others(41): Show | 45 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.326-34052_326-3403 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(9): Show |
48 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(45): Show | 48 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.326-34054_326-3403 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(11): Show |
16 | a0001c0001t0002g0031a0001c0001t0002g0133a0001c0001t0002g0202others(13): Show | 16 | HG00621.hp1 HG01099.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.326-34056_326-3403 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(13): Show |
10 | a0001c0001t0002g0218a0001c0001t0005g0094a0001c0001t0006g0185others(7): Show | 10 | HG00323.hp1 HG01106.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.326-34058_326-3403 others(24): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
C | CTGTGTGT others(19): Show |
1 | a0001c0001t0029g0135 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326-34064_326-3403 others(30): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
CTG | C | 33 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(30): Show | 34 | HG00639.hp2 HG00673.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.326-34040_326-3403 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
CTGTG | C | 7 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(4): Show | 7 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-34042_326-3403 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344568
|
CTGTGTG | C | 9 | a0001c0001t0005g0237a0001c0001t0026g0247a0001c0001t0026g0248others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.326-34044_326-3403 others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344568 | ||||||
| chr5:44344747
|
T | C | 1 | a0001c0001t0075g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.326-34217A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344747 | ||||||
| chr5:44344905
|
C | T | 1 | a0001c0001t0004g0067 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.326-34375G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44344905 | ||||||
| chr5:44345042
|
T | C | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-34512A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345042 | ||||||
| chr5:44345098
|
A | T | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-34568T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345098 | ||||||
| chr5:44345313
|
AACAAATA others(39): Show |
A | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-34829_326-3478 others(50): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345313 | ||||||
| chr5:44345438
|
T | C | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.326-34908A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345438 | ||||||
| chr5:44345443
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.326-34913T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345443 | ||||||
| chr5:44345456
|
A | G | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-34926T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345456 | ||||||
| chr5:44345469
|
T | C | 3 | a0001c0001t0002g0320a0001c0001t0002g0323a0001c0001t0002g0328 | 3 | HG02083.hp2 NA18946.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.326-34939A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345469 | ||||||
| chr5:44345570
|
C | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.326-35040G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345570 | ||||||
| chr5:44345633
|
C | CA | 6 | a0001c0001t0005g0237a0001c0001t0010g0251a0001c0001t0019g0263others(3): Show | 6 | HG02280.hp1 HG03041.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.326-35104dupT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345633 | ||||||
| chr5:44345633
|
CA | C | 143 | a0001c0001t0001g0326a0001c0001t0002g0031a0001c0001t0002g0034others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.326-35104delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345633 | ||||||
| chr5:44345633
|
CAA | C | 73 | a0001c0001t0003g0147a0001c0001t0004g0033a0001c0001t0004g0043others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326-35105_326-3510 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345633 | ||||||
| chr5:44345820
|
C | G | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326-35290G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345820 | ||||||
| chr5:44346064
|
T | C | 2 | a0001c0001t0018g0109a0001c0001t0023g0004 | 3 | HG01515.hp2 HG01517.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.326-35534A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346064 | ||||||
| chr5:44346270
|
A | C | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-35740T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346270 | ||||||
| chr5:44346279
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-35749G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346279 | ||||||
| chr5:44346284
|
T | A | 1 | a0001c0002t0005g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.326-35754A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346284 | ||||||
| chr5:44346444
|
A | G | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.326-35914T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346444 | ||||||
| chr5:44346498
|
A | G | 1 | a0003c0004t0038g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.326-35968T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346498 | ||||||
| chr5:44346534
|
C | T | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326-36004G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346534 | ||||||
| chr5:44346634
|
T | A | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-36104A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346634 | ||||||
| chr5:44346643
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.326-36113G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346643 | ||||||
| chr5:44346672
|
C | T | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.326-36142G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346672 | ||||||
| chr5:44346708
|
C | T | 8 | a0001c0001t0002g0158a0001c0001t0026g0247a0001c0001t0026g0248others(5): Show | 8 | HG00673.hp2 HG01109.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-36178G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346708 | ||||||
| chr5:44346810
|
T | C | 8 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 8 | HG00544.hp1 HG02165.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.326-36280A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346810 | ||||||
| chr5:44346923
|
C | A | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326-36393G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44346923 | ||||||
| chr5:44347029
|
T | C | 115 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(112): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.326-36499A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347029 | ||||||
| chr5:44347232
|
C | T | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-36702G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347232 | ||||||
| chr5:44347482
|
G | A | 7 | a0001c0001t0024g0121a0001c0001t0024g0338a0001c0001t0024g0339others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-36952C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347482 | ||||||
| chr5:44347689
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-37159G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347689 | ||||||
| chr5:44347760
|
C | A | 1 | a0001c0001t0003g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.326-37230G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347760 | ||||||
| chr5:44347760
|
C | T | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.326-37230G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347760 | ||||||
| chr5:44347937
|
G | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0333 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.326-37407C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347937 | ||||||
| chr5:44347984
|
C | A | 1 | a0001c0001t0006g0124 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.326-37454G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44347984 | ||||||
| chr5:44348278
|
T | C | 1 | a0001c0001t0060g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.326-37748A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348278 | ||||||
| chr5:44348420
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.326-37890T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348420 | ||||||
| chr5:44348550
|
C | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-38020G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348550 | ||||||
| chr5:44348674
|
GC | G | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-38145delG | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348674 | ||||||
| chr5:44348676
|
T | A | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326-38146A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348676 | ||||||
| chr5:44348687
|
A | C | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.326-38157T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348687 | ||||||
| chr5:44348688
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.326-38158C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348688 | ||||||
| chr5:44348799
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-38269A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348799 | ||||||
| chr5:44348846
|
T | C | 1 | a0001c0001t0005g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326-38316A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348846 | ||||||
| chr5:44348885
|
C | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.326-38355G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348885 | ||||||
| chr5:44348916
|
A | T | 1 | a0001c0001t0003g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.326-38386T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44348916 | ||||||
| chr5:44349017
|
T | C | 1 | a0001c0001t0006g0220 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.326-38487A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349017 | ||||||
| chr5:44349039
|
A | T | 131 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(128): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.326-38509T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349039 | ||||||
| chr5:44349140
|
G | C | 1 | a0001c0001t0037g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.326-38610C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349140 | ||||||
| chr5:44349209
|
T | C | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-38679A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349209 | ||||||
| chr5:44349422
|
T | A | 2 | a0001c0001t0007g0047a0001c0001t0007g0284 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.326-38892A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
T | TTA | 5 | a0001c0001t0010g0258a0001c0001t0010g0271a0001c0001t0012g0027others(2): Show | 5 | HG01952.hp2 HG03139.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.326-38894_326-3889 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
T | TTATA | 6 | a0001c0001t0010g0267a0001c0001t0011g0262a0001c0001t0012g0029others(3): Show | 6 | HG01884.hp1 HG02257.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-38896_326-3889 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
T | TTATATA | 4 | a0001c0001t0010g0253a0001c0001t0033g0270a0001c0001t0034g0275others(1): Show | 4 | HG00639.hp2 HG01358.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-38898_326-3889 others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTA | T | 3 | a0001c0001t0011g0256a0001c0001t0011g0259a0001c0001t0066g0181 | 3 | HG02071.hp1 NA18951.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.326-38894_326-3889 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0032g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.326-38910_326-3889 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0032g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.326-38912_326-3889 others(24): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0012g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325+38910_326-3889 others(30): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTATATAT others(27): Show |
T | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+38902_326-3889 others(38): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349422
|
TTATATAT others(45): Show |
T | 2 | a0001c0001t0002g0189a0001c0001t0006g0155 | 2 | HG00597.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.325+38884_326-3889 others(56): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349422 | ||||||
| chr5:44349431
|
TATATATA others(35): Show |
T | 1 | a0001c0001t0015g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.325+38885_326-3890 others(46): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349431 | ||||||
| chr5:44349433
|
TATATATA others(33): Show |
T | 1 | a0001c0001t0039g0224 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.325+38885_326-3890 others(44): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349433 | ||||||
| chr5:44349439
|
T | TATATATA others(7): Show |
1 | a0001c0001t0017g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.326-38910_326-3890 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349439 | ||||||
| chr5:44349439
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.326-38910_326-3890 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349439 | ||||||
| chr5:44349439
|
TATATATA others(27): Show |
T | 2 | a0001c0001t0003g0137a0001c0001t0010g0251 | 2 | NA19006.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.325+38885_326-3891 others(38): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349439 | ||||||
| chr5:44349443
|
T | TATATATA others(9): Show |
3 | a0001c0001t0020g0058a0001c0001t0020g0240a0001c0001t0020g0241 | 3 | HG01891.hp2 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.325+38914_326-3891 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349443 | ||||||
| chr5:44349443
|
T | TATATATA others(7): Show |
1 | a0001c0001t0020g0239 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.325+38914_326-3891 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349443 | ||||||
| chr5:44349443
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0002g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325+38885_325+3891 others(34): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349443 | ||||||
| chr5:44349445
|
TATATATA others(21): Show |
T | 9 | a0001c0001t0005g0041a0001c0001t0005g0055a0001c0001t0005g0290others(6): Show | 10 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.325+38885_325+3891 others(32): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349445 | ||||||
| chr5:44349447
|
TATATATA others(19): Show |
T | 3 | a0001c0001t0005g0044a0001c0001t0007g0281a0001c0001t0030g0211 | 3 | HG03486.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.325+38885_325+3891 others(30): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349447 | ||||||
| chr5:44349449
|
T | TATATATA others(49): Show |
1 | a0001c0001t0073g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(60): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(43): Show |
1 | a0001c0001t0074g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.325+38908_325+3890 others(54): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(15): Show |
1 | a0001c0001t0008g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(49): Show |
1 | a0001c0001t0075g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(60): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(45): Show |
1 | a0001c0001t0026g0247 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(56): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(43): Show |
1 | a0001c0001t0026g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(54): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
T | TATATATA others(39): Show |
1 | a0001c0001t0026g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325+38908_325+3890 others(50): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349449
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0005g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.325+38885_325+3890 others(28): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349449 | ||||||
| chr5:44349451
|
T | TATATATA others(21): Show |
1 | a0001c0001t0008g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.325+38906_325+3890 others(32): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
T | TATATATA others(17): Show |
2 | a0001c0001t0008g0099a0001c0001t0051g0097 | 2 | HG00733.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.325+38906_325+3890 others(28): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
T | TATATATA others(13): Show |
1 | a0001c0001t0008g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.325+38906_325+3890 others(24): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
T | TATATATA others(11): Show |
1 | a0001c0001t0008g0100 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.325+38906_325+3890 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
T | TATATATA others(7): Show |
3 | a0001c0001t0008g0096a0001c0001t0008g0101a0001c0001t0045g0016 | 3 | HG01123.hp1 HG01258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.325+38906_325+3890 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
T | TCAGAATA others(15): Show |
1 | a0001c0001t0017g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.325+38906_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349451
|
TATATATA others(15): Show |
T | 9 | a0001c0001t0003g0138a0001c0001t0004g0051a0001c0001t0004g0056others(6): Show | 9 | HG00438.hp1 HG01975.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+38885_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349451 | ||||||
| chr5:44349453
|
T | TATATATA others(19): Show |
1 | a0001c0001t0023g0004 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.325+38904_325+3890 others(30): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATATATA others(15): Show |
1 | a0001c0001t0061g0115 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.325+38904_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATATATA others(7): Show |
2 | a0001c0001t0003g0108a0001c0001t0018g0105 | 2 | HG01981.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.325+38904_325+3890 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATATATA others(5): Show |
4 | a0001c0001t0018g0103a0001c0001t0018g0106a0001c0001t0046g0028others(1): Show | 4 | HG01192.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+38904_325+3890 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATATATC others(3): Show |
1 | a0001c0001t0018g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.325+38904_325+3890 others(14): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATCAGAA others(17): Show |
17 | a0001c0001t0001g0212a0001c0001t0001g0244a0001c0001t0001g0245others(14): Show | 17 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.325+38904_325+3890 others(28): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TATCAGAA others(55): Show |
1 | a0001c0001t0057g0312 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.325+38904_325+3890 others(66): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TCAGAATA others(41): Show |
1 | a0001c0001t0001g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.325+38904_325+3890 others(52): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
T | TCAGAATA others(15): Show |
35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(32): Show | 39 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.325+38904_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349453
|
TATATATA others(13): Show |
T | 13 | a0001c0001t0002g0202a0001c0001t0002g0218a0001c0001t0002g0225others(10): Show | 13 | HG01106.hp1 HG01123.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.325+38885_325+3890 others(24): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349453 | ||||||
| chr5:44349454
|
A | G | 2 | a0001c0001t0001g0319a0001c0001t0001g0334 | 2 | NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.325+38904T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349454 | ||||||
| chr5:44349455
|
T | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0334 | 2 | NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.325+38903A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349455 | ||||||
| chr5:44349455
|
T | TATATATA others(15): Show |
1 | a0001c0001t0011g0266 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.325+38902_325+3890 others(26): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349455 | ||||||
| chr5:44349455
|
T | TATATATA others(11): Show |
1 | a0001c0001t0019g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.325+38885_325+3890 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349455 | ||||||
| chr5:44349455
|
TATATATA others(11): Show |
T | 19 | a0001c0001t0002g0031a0001c0001t0002g0221a0001c0001t0003g0147others(16): Show | 19 | HG00735.hp1 HG01175.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.325+38885_325+3890 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349455 | ||||||
| chr5:44349457
|
T | TATATATA others(31): Show |
4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0022g0242others(1): Show | 4 | HG01361.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+38900_325+3890 others(42): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349457 | ||||||
| chr5:44349457
|
T | TCAGA | 4 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+38900_325+3890 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349457 | ||||||
| chr5:44349457
|
TATATATA others(9): Show |
T | 30 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(27): Show | 30 | HG00544.hp2 HG00733.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.325+38885_325+3890 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349457 | ||||||
| chr5:44349459
|
TATATATA others(7): Show |
T | 50 | a0001c0001t0002g0128a0001c0001t0002g0133a0001c0001t0002g0134others(47): Show | 50 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.325+38885_325+3889 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349459 | ||||||
| chr5:44349461
|
TATATATA others(5): Show |
T | 35 | a0001c0001t0002g0146a0001c0001t0002g0156a0001c0001t0002g0160others(32): Show | 35 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.325+38885_325+3889 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349461 | ||||||
| chr5:44349463
|
TATATATC others(3): Show |
T | 11 | a0001c0001t0002g0129a0001c0001t0003g0005a0001c0001t0003g0148others(8): Show | 12 | HG01069.hp1 HG03225.hp2 NA18977.hp2 others(9): Show |
intron_variant | MODIFIER | c.325+38885_325+3889 others(14): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349463 | ||||||
| chr5:44349465
|
TATATCAG others(1): Show |
T | 10 | a0001c0001t0002g0130a0001c0001t0003g0132a0001c0001t0003g0161others(7): Show | 10 | HG01361.hp2 HG01952.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.325+38885_325+3889 others(12): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349465 | ||||||
| chr5:44349467
|
TATCAGA | T | 3 | a0001c0001t0003g0200a0001c0001t0004g0075a0001c0001t0006g0227 | 3 | NA18965.hp1 NA18971.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.325+38885_325+3889 others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349467 | ||||||
| chr5:44349469
|
TCAGA | T | 4 | a0001c0001t0003g0201a0001c0001t0006g0185a0001c0001t0038g0068others(1): Show | 4 | HG03225.hp1 NA18612.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+38885_325+3888 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349469 | ||||||
| chr5:44349470
|
CAGAATAT others(9): Show |
C | 3 | a0001c0001t0009g0018a0001c0001t0009g0020a0001c0001t0047g0024 | 3 | HG01884.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.325+38872_325+3888 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349470 | ||||||
| chr5:44349486
|
A | C | 9 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0009g0015others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.325+38872T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349486 | ||||||
| chr5:44349491
|
A | AAT | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 84 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.325+38865_325+3886 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349491 | ||||||
| chr5:44349491
|
A | AATATATA others(33): Show |
2 | a0001c0001t0001g0299a0001c0001t0013g0300 | 2 | HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.325+38866_325+3886 others(44): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349491 | ||||||
| chr5:44349521
|
T | C | 2 | a0001c0001t0030g0120a0001c0001t0062g0178 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.325+38837A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349521 | ||||||
| chr5:44349586
|
A | T | 2 | a0001c0001t0013g0112a0001c0001t0013g0113 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.325+38772T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349586 | ||||||
| chr5:44349688
|
TA | T | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+38669delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349688 | ||||||
| chr5:44349832
|
T | C | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+38526A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349832 | ||||||
| chr5:44350128
|
A | T | 12 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0009g0015others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.325+38230T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350128 | ||||||
| chr5:44350233
|
C | T | 6 | a0001c0002t0005g0049a0001c0002t0005g0050a0001c0002t0005g0052others(3): Show | 6 | HG01167.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.325+38125G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350233 | ||||||
| chr5:44350420
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.325+37938G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350420 | ||||||
| chr5:44350582
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.325+37776A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350582 | ||||||
| chr5:44350625
|
C | T | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+37733G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350625 | ||||||
| chr5:44350644
|
T | C | 11 | a0001c0001t0003g0108a0001c0001t0018g0103a0001c0001t0018g0105others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.325+37714A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350644 | ||||||
| chr5:44350692
|
C | A | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+37666G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350692 | ||||||
| chr5:44350726
|
C | T | 1 | a0001c0001t0015g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.325+37632G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350726 | ||||||
| chr5:44350816
|
G | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.325+37542C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44350816 | ||||||
| chr5:44351052
|
T | C | 7 | a0001c0001t0024g0121a0001c0001t0024g0338a0001c0001t0024g0339others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+37306A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351052 | ||||||
| chr5:44351156
|
G | T | 1 | a0001c0001t0014g0076 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325+37202C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351156 | ||||||
| chr5:44351232
|
A | C | 1 | a0001c0001t0003g0108 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.325+37126T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351232 | ||||||
| chr5:44351549
|
G | A | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.325+36809C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351549 | ||||||
| chr5:44351567
|
A | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+36791T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351567 | ||||||
| chr5:44351573
|
T | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+36785A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351573 | ||||||
| chr5:44351896
|
A | G | 1 | a0001c0001t0007g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.325+36462T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351896 | ||||||
| chr5:44351909
|
C | T | 1 | a0001c0001t0008g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.325+36449G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44351909 | ||||||
| chr5:44352117
|
G | A | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+36241C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352117 | ||||||
| chr5:44352227
|
G | A | 1 | a0001c0001t0008g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.325+36131C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352227 | ||||||
| chr5:44352242
|
T | C | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+36116A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352242 | ||||||
| chr5:44352273
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.325+36085T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352273 | ||||||
| chr5:44352623
|
G | A | 1 | a0001c0001t0073g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325+35735C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352623 | ||||||
| chr5:44352650
|
A | G | 1 | a0001c0001t0032g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.325+35708T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352650 | ||||||
| chr5:44352857
|
T | C | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.325+35501A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352857 | ||||||
| chr5:44352965
|
G | T | 1 | a0001c0001t0051g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325+35393C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352965 | ||||||
| chr5:44352998
|
G | A | 1 | a0001c0001t0010g0267 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.325+35360C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44352998 | ||||||
| chr5:44353062
|
A | C | 1 | a0001c0001t0010g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.325+35296T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353062 | ||||||
| chr5:44353296
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.325+35062A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353296 | ||||||
| chr5:44353425
|
C | T | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.325+34933G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353425 | ||||||
| chr5:44353428
|
T | A | 1 | a0001c0001t0055g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.325+34930A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353428 | ||||||
| chr5:44353481
|
C | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0188a0001c0001t0006g0227 | 3 | NA18940.hp1 NA18965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.325+34877G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353481 | ||||||
| chr5:44353519
|
C | T | 205 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(202): Show | 207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.325+34839G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353519 | ||||||
| chr5:44353699
|
A | G | 18 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(15): Show | 18 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.325+34659T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353699 | ||||||
| chr5:44353742
|
C | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.325+34616G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353742 | ||||||
| chr5:44353759
|
C | A | 4 | a0001c0001t0016g0170a0001c0001t0021g0136a0001c0001t0021g0168others(1): Show | 4 | NA18953.hp1 NA18977.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+34599G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353759 | ||||||
| chr5:44353808
|
G | C | 2 | a0001c0001t0002g0031a0001c0001t0006g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.325+34550C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353808 | ||||||
| chr5:44353809
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.325+34549C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353809 | ||||||
| chr5:44353883
|
G | A | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+34475C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44353883 | ||||||
| chr5:44354052
|
G | T | 1 | a0001c0001t0043g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.325+34306C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354052 | ||||||
| chr5:44354105
|
C | T | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+34253G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354105 | ||||||
| chr5:44354408
|
C | G | 1 | a0001c0001t0028g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325+33950G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354408 | ||||||
| chr5:44354414
|
T | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+33944A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354414 | ||||||
| chr5:44354509
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.325+33849G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354509 | ||||||
| chr5:44354641
|
A | C | 1 | a0001c0001t0003g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.325+33717T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354641 | ||||||
| chr5:44354786
|
T | C | 2 | a0001c0001t0018g0109a0001c0001t0023g0004 | 3 | HG01515.hp2 HG01517.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.325+33572A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354786 | ||||||
| chr5:44354824
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.325+33534T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354824 | ||||||
| chr5:44354950
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+33408G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354950 | ||||||
| chr5:44354951
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+33407G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354951 | ||||||
| chr5:44354960
|
T | C | 1 | a0001c0001t0053g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.325+33398A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44354960 | ||||||
| chr5:44355224
|
T | C | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+33134A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355224 | ||||||
| chr5:44355228
|
T | C | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+33130A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355228 | ||||||
| chr5:44355253
|
C | G | 1 | a0001c0001t0007g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.325+33105G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355253 | ||||||
| chr5:44355261
|
T | C | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+33097A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355261 | ||||||
| chr5:44355301
|
A | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+33057T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355301 | ||||||
| chr5:44355364
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.325+32994A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355364 | ||||||
| chr5:44355469
|
T | C | 1 | a0001c0001t0072g0340 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.325+32889A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355469 | ||||||
| chr5:44355519
|
A | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 65 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.325+32839T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355519 | ||||||
| chr5:44355520
|
A | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0055g0228 | 3 | HG01167.hp1 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.325+32838T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355520 | ||||||
| chr5:44355664
|
G | T | 2 | a0001c0001t0010g0251a0001c0001t0032g0252 | 2 | NA19006.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325+32694C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355664 | ||||||
| chr5:44355809
|
A | G | 331 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(328): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.325+32549T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355809 | ||||||
| chr5:44355871
|
A | G | 1 | a0001c0001t0007g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.325+32487T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355871 | ||||||
| chr5:44355948
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.325+32410A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355948 | ||||||
| chr5:44355964
|
G | A | 2 | a0001c0001t0008g0096a0001c0001t0008g0101 | 2 | HG01123.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.325+32394C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355964 | ||||||
| chr5:44356245
|
T | A | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+32113A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356245 | ||||||
| chr5:44356288
|
C | T | 339 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(336): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.325+32070G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356288 | ||||||
| chr5:44356650
|
T | G | 1 | a0001c0001t0023g0116 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.325+31708A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356650 | ||||||
| chr5:44356674
|
T | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+31684A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356674 | ||||||
| chr5:44356953
|
C | T | 17 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(14): Show | 17 | HG01109.hp2 HG01361.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325+31405G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356953 | ||||||
| chr5:44357004
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.325+31354C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357004 | ||||||
| chr5:44357118
|
TA | T | 208 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(205): Show | 210 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.325+31239delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357118 | ||||||
| chr5:44357120
|
A | T | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+31238T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357120 | ||||||
| chr5:44357675
|
A | G | 1 | a0001c0001t0010g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.325+30683T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357675 | ||||||
| chr5:44357705
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.325+30653C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357705 | ||||||
| chr5:44357807
|
A | G | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+30551T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357807 | ||||||
| chr5:44357887
|
C | A | 3 | a0001c0001t0005g0237a0001c0001t0028g0249a0001c0001t0028g0250 | 3 | HG03041.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+30471G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357887 | ||||||
| chr5:44357953
|
G | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+30405C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357953 | ||||||
| chr5:44357996
|
G | A | 1 | a0001c0001t0060g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.325+30362C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357996 | ||||||
| chr5:44358149
|
T | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+30209A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358149 | ||||||
| chr5:44358274
|
T | C | 2 | a0001c0001t0001g0313a0001c0001t0017g0311 | 2 | NA18974.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.325+30084A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358274 | ||||||
| chr5:44358392
|
G | C | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+29966C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358392 | ||||||
| chr5:44358676
|
C | T | 26 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(23): Show | 26 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.325+29682G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358676 | ||||||
| chr5:44358708
|
G | T | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+29650C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358708 | ||||||
| chr5:44358762
|
G | A | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+29596C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358762 | ||||||
| chr5:44358794
|
C | T | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+29564G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358794 | ||||||
| chr5:44358799
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+29559C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358799 | ||||||
| chr5:44358813
|
A | G | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+29545T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358813 | ||||||
| chr5:44358839
|
A | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.325+29519T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358839 | ||||||
| chr5:44359053
|
T | G | 2 | a0001c0001t0005g0044a0001c0001t0005g0045 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.325+29305A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359053 | ||||||
| chr5:44359197
|
A | G | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+29161T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359197 | ||||||
| chr5:44359235
|
A | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+29123T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359235 | ||||||
| chr5:44359238
|
T | C | 18 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(15): Show | 18 | HG01109.hp2 HG01346.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.325+29120A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359238 | ||||||
| chr5:44359326
|
C | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.325+29032G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359326 | ||||||
| chr5:44359372
|
T | C | 16 | a0001c0001t0002g0165a0001c0001t0002g0184a0001c0001t0002g0197others(13): Show | 16 | HG00544.hp2 HG02056.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.325+28986A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359372 | ||||||
| chr5:44359392
|
A | G | 1 | a0001c0001t0006g0155 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.325+28966T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359392 | ||||||
| chr5:44359424
|
C | A | 46 | a0001c0001t0005g0237a0001c0001t0010g0251a0001c0001t0010g0253others(43): Show | 46 | HG00639.hp2 HG00673.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.325+28934G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359424 | ||||||
| chr5:44359534
|
A | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.325+28824T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359534 | ||||||
| chr5:44359722
|
T | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+28636A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359722 | ||||||
| chr5:44359944
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.325+28414G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44359944 | ||||||
| chr5:44360112
|
C | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0299a0001c0001t0013g0300 | 3 | HG01074.hp2 HG01081.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.325+28246G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44360112 | ||||||
| chr5:44360790
|
C | T | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+27568G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44360790 | ||||||
| chr5:44360846
|
A | G | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+27512T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44360846 | ||||||
| chr5:44360928
|
C | G | 1 | a0001c0001t0063g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.325+27430G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44360928 | ||||||
| chr5:44360937
|
G | T | 1 | a0001c0001t0046g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325+27421C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44360937 | ||||||
| chr5:44361071
|
G | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+27287C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361071 | ||||||
| chr5:44361116
|
G | C | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+27242C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361116 | ||||||
| chr5:44361150
|
C | A | 1 | a0001c0001t0013g0308 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.325+27208G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361150 | ||||||
| chr5:44361349
|
G | A | 3 | a0001c0001t0004g0283a0001c0001t0007g0284a0001c0001t0007g0291 | 3 | HG02723.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.325+27009C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361349 | ||||||
| chr5:44361404
|
G | A | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.325+26954C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361404 | ||||||
| chr5:44361528
|
G | A | 1 | a0001c0001t0011g0256 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.325+26830C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361528 | ||||||
| chr5:44361683
|
C | T | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+26675G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361683 | ||||||
| chr5:44361771
|
T | A | 1 | a0001c0001t0016g0170 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.325+26587A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361771 | ||||||
| chr5:44361928
|
C | T | 6 | a0001c0001t0016g0142a0001c0001t0016g0167a0001c0001t0016g0170others(3): Show | 6 | NA18953.hp1 NA18977.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+26430G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44361928 | ||||||
| chr5:44362032
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.325+26326G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362032 | ||||||
| chr5:44362102
|
G | A | 36 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(33): Show | 36 | HG00733.hp1 HG01069.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.325+26256C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362102 | ||||||
| chr5:44362236
|
T | C | 338 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.325+26122A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362236 | ||||||
| chr5:44362333
|
C | T | 4 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0033g0257others(1): Show | 4 | HG00639.hp2 HG01257.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+26025G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362333 | ||||||
| chr5:44362436
|
G | A | 133 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(130): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.325+25922C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362436 | ||||||
| chr5:44362458
|
A | G | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+25900T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362458 | ||||||
| chr5:44362667
|
C | T | 133 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(130): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.325+25691G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362667 | ||||||
| chr5:44362818
|
T | C | 338 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.325+25540A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362818 | ||||||
| chr5:44362922
|
G | A | 1 | a0001c0001t0007g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.325+25436C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362922 | ||||||
| chr5:44363240
|
A | G | 1 | a0001c0001t0028g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325+25118T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363240 | ||||||
| chr5:44363241
|
C | T | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+25117G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363241 | ||||||
| chr5:44363475
|
A | T | 13 | a0001c0001t0004g0033a0001c0001t0004g0064a0001c0001t0004g0065others(10): Show | 13 | HG00438.hp1 HG02056.hp2 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.325+24883T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363475 | ||||||
| chr5:44363476
|
A | T | 13 | a0001c0001t0004g0033a0001c0001t0004g0064a0001c0001t0004g0065others(10): Show | 13 | HG00438.hp1 HG02056.hp2 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.325+24882T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363476 | ||||||
| chr5:44363533
|
C | A | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+24825G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363533 | ||||||
| chr5:44363588
|
A | G | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.325+24770T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363588 | ||||||
| chr5:44363689
|
C | G | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325+24669G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363689 | ||||||
| chr5:44363905
|
A | T | 206 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(203): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.325+24453T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363905 | ||||||
| chr5:44363996
|
A | T | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+24362T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363996 | ||||||
| chr5:44364158
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325+24200A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364158 | ||||||
| chr5:44364520
|
G | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+23838C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364520 | ||||||
| chr5:44364569
|
A | G | 1 | a0001c0001t0006g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.325+23789T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364569 | ||||||
| chr5:44364719
|
C | T | 1 | a0001c0001t0026g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325+23639G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364719 | ||||||
| chr5:44364720
|
G | A | 1 | a0001c0001t0006g0032 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.325+23638C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364720 | ||||||
| chr5:44364844
|
T | A | 1 | a0001c0001t0005g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.325+23514A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364844 | ||||||
| chr5:44364861
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.325+23497C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364861 | ||||||
| chr5:44364921
|
C | T | 1 | a0001c0001t0022g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.325+23437G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364921 | ||||||
| chr5:44364976
|
T | C | 26 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(23): Show | 26 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.325+23382A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44364976 | ||||||
| chr5:44365083
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.325+23275C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365083 | ||||||
| chr5:44365312
|
C | T | 12 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0009g0015others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.325+23046G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365312 | ||||||
| chr5:44365350
|
C | CA | 88 | a0001c0001t0002g0151a0001c0001t0004g0033a0001c0001t0004g0043others(85): Show | 90 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.325+23007dupT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365350 | ||||||
| chr5:44365350
|
C | CAA | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.325+23006_325+2300 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365350 | ||||||
| chr5:44365350
|
C | CAAA | 21 | a0001c0001t0002g0031a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 21 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.325+23005_325+2300 others(7): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365350 | ||||||
| chr5:44365387
|
T | C | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.325+22971A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365387 | ||||||
| chr5:44365443
|
C | A | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+22915G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365443 | ||||||
| chr5:44365531
|
C | T | 287 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.325+22827G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365531 | ||||||
| chr5:44365538
|
T | C | 1 | a0001c0001t0006g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.325+22820A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365538 | ||||||
| chr5:44365946
|
G | A | 339 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(336): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.325+22412C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365946 | ||||||
| chr5:44365959
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.325+22399G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365959 | ||||||
| chr5:44365960
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.325+22398C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365960 | ||||||
| chr5:44366127
|
C | CT | 151 | a0001c0001t0002g0031a0001c0001t0002g0035a0001c0001t0002g0128others(148): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.325+22230dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366127 | ||||||
| chr5:44366127
|
C | CTT | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 81 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.325+22229_325+2223 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366127 | ||||||
| chr5:44366127
|
C | CTTT | 37 | a0001c0001t0001g0246a0001c0001t0001g0294a0001c0001t0001g0299others(34): Show | 37 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.325+22228_325+2223 others(7): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366127 | ||||||
| chr5:44366127
|
C | CTTTT | 13 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(10): Show | 14 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.325+22227_325+2223 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366127 | ||||||
| chr5:44366280
|
G | A | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+22078C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366280 | ||||||
| chr5:44366329
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.325+22029A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366329 | ||||||
| chr5:44366450
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.325+21908C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366450 | ||||||
| chr5:44366671
|
A | T | 1 | a0001c0001t0019g0254 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.325+21687T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366671 | ||||||
| chr5:44366677
|
T | G | 1 | a0001c0001t0030g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.325+21681A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366677 | ||||||
| chr5:44366740
|
A | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+21618T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366740 | ||||||
| chr5:44366747
|
G | A | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+21611C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366747 | ||||||
| chr5:44367119
|
A | T | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+21239T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367119 | ||||||
| chr5:44367300
|
G | A | 7 | a0001c0001t0026g0247a0001c0001t0026g0248a0001c0001t0026g0278others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+21058C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367300 | ||||||
| chr5:44367843
|
GT | G | 310 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.325+20514delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367843 | ||||||
| chr5:44367843
|
GTT | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(5): Show | 9 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+20513_325+2051 others(6): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367843 | ||||||
| chr5:44367843
|
GTTT | G | 11 | a0001c0001t0005g0237a0001c0001t0020g0058a0001c0001t0020g0239others(8): Show | 11 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.325+20512_325+2051 others(7): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367843 | ||||||
| chr5:44368007
|
T | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+20351A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368007 | ||||||
| chr5:44368021
|
G | A | 132 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+20337C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368021 | ||||||
| chr5:44368148
|
G | T | 73 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(70): Show | 74 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.325+20210C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368148 | ||||||
| chr5:44368373
|
CT | C | 13 | a0001c0001t0003g0108a0001c0001t0013g0112a0001c0001t0013g0113others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.325+19984delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368373 | ||||||
| chr5:44368404
|
T | C | 207 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(204): Show | 209 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.325+19954A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368404 | ||||||
| chr5:44368440
|
T | C | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+19918A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368440 | ||||||
| chr5:44368500
|
C | T | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+19858G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368500 | ||||||
| chr5:44368673
|
G | T | 72 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(69): Show | 73 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.325+19685C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368673 | ||||||
| chr5:44368789
|
T | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+19569A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368789 | ||||||
| chr5:44368822
|
T | C | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325+19536A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368822 | ||||||
| chr5:44368955
|
A | C | 1 | a0001c0001t0004g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.325+19403T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368955 | ||||||
| chr5:44368978
|
A | C | 7 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+19380T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368978 | ||||||
| chr5:44369318
|
G | A | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+19040C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44369318 | ||||||
| chr5:44369451
|
C | T | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.325+18907G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44369451 | ||||||
| chr5:44369550
|
T | C | 1 | a0001c0001t0059g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.325+18808A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44369550 | ||||||
| chr5:44369554
|
C | T | 131 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(128): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.325+18804G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44369554 | ||||||
| chr5:44370062
|
G | C | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+18296C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44370062 | ||||||
| chr5:44370187
|
C | A | 1 | a0001c0001t0019g0268 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.325+18171G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44370187 | ||||||
| chr5:44370328
|
C | T | 2 | a0001c0001t0006g0185a0001c0001t0006g0186 | 2 | NA18995.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.325+18030G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44370328 | ||||||
| chr5:44370843
|
C | G | 1 | a0001c0001t0001g0335 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.325+17515G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44370843 | ||||||
| chr5:44370974
|
C | T | 3 | a0001c0001t0005g0237a0001c0001t0028g0249a0001c0001t0028g0250 | 3 | HG03041.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+17384G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44370974 | ||||||
| chr5:44371124
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325+17234G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371124 | ||||||
| chr5:44371127
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325+17231A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371127 | ||||||
| chr5:44371129
|
C | T | 74 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(71): Show | 75 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.325+17229G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371129 | ||||||
| chr5:44371255
|
G | A | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG01975.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.325+17103C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371255 | ||||||
| chr5:44371296
|
T | C | 278 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(275): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.325+17062A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371296 | ||||||
| chr5:44371356
|
T | G | 1 | a0001c0001t0018g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.325+17002A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371356 | ||||||
| chr5:44371388
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+16970G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371388 | ||||||
| chr5:44371419
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0006g0145 | 2 | HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.325+16939C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371419 | ||||||
| chr5:44371492
|
C | T | 278 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(275): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.325+16866G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371492 | ||||||
| chr5:44371565
|
G | T | 1 | a0001c0001t0027g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.325+16793C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371565 | ||||||
| chr5:44371567
|
A | G | 123 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(120): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.325+16791T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371567 | ||||||
| chr5:44371827
|
T | C | 2 | a0001c0001t0022g0183a0001c0001t0041g0013 | 2 | HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.325+16531A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371827 | ||||||
| chr5:44372074
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.325+16284G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372074 | ||||||
| chr5:44372088
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0002g0144 | 2 | HG02129.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.325+16270G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372088 | ||||||
| chr5:44372197
|
C | T | 1 | a0001c0001t0073g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325+16161G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372197 | ||||||
| chr5:44372218
|
TGCCACAT others(6): Show |
T | 1 | a0001c0001t0048g0255 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.325+16127_325+1613 others(17): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372218 | ||||||
| chr5:44372263
|
A | G | 8 | a0001c0001t0020g0058a0001c0001t0020g0239a0001c0001t0020g0240others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.325+16095T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372263 | ||||||
| chr5:44372325
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.325+16033G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372325 | ||||||
| chr5:44372738
|
G | A | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+15620C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372738 | ||||||
| chr5:44372762
|
T | C | 333 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+15596A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372762 | ||||||
| chr5:44372958
|
C | T | 104 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0035others(101): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.325+15400G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372958 | ||||||
| chr5:44373089
|
G | T | 1 | a0001c0001t0002g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.325+15269C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373089 | ||||||
| chr5:44373135
|
C | T | 1 | a0001c0001t0028g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325+15223G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373135 | ||||||
| chr5:44373155
|
G | A | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+15203C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373155 | ||||||
| chr5:44373202
|
C | A | 1 | a0001c0001t0011g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.325+15156G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373202 | ||||||
| chr5:44373325
|
C | T | 1 | a0001c0001t0063g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.325+15033G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373325 | ||||||
| chr5:44373563
|
C | T | 1 | a0001c0001t0016g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.325+14795G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373563 | ||||||
| chr5:44373574
|
G | A | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+14784C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373574 | ||||||
| chr5:44373607
|
C | T | 28 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(25): Show | 28 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.325+14751G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373607 | ||||||
| chr5:44373657
|
A | G | 75 | a0001c0001t0004g0033a0001c0001t0004g0043a0001c0001t0004g0051others(72): Show | 76 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.325+14701T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373657 | ||||||
| chr5:44373705
|
T | C | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.325+14653A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44373705 | ||||||
| chr5:44374184
|
T | C | 1 | a0001c0001t0032g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.325+14174A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374184 | ||||||
| chr5:44374242
|
G | A | 1 | a0001c0001t0045g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.325+14116C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374242 | ||||||
| chr5:44374284
|
G | C | 205 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(202): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.325+14074C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374284 | ||||||
| chr5:44374434
|
A | G | 1 | a0001c0001t0007g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.325+13924T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374434 | ||||||
| chr5:44374549
|
T | C | 1 | a0001c0001t0008g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.325+13809A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374549 | ||||||
| chr5:44374873
|
T | A | 17 | a0001c0001t0005g0055a0001c0001t0009g0015a0001c0001t0009g0017others(14): Show | 17 | HG01192.hp1 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.325+13485A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374873 | ||||||
| chr5:44374875
|
A | G | 1 | a0001c0001t0042g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.325+13483T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374875 | ||||||
| chr5:44374885
|
A | AT | 320 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.325+13472dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374885 | ||||||
| chr5:44375104
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.325+13254G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44375104 | ||||||
| chr5:44375168
|
C | G | 107 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(104): Show | 110 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.325+13190G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44375168 | ||||||
| chr5:44375405
|
G | A | 1 | a0001c0001t0042g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.325+12953C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44375405 | ||||||
| chr5:44375527
|
G | A | 2 | a0001c0001t0007g0047a0001c0001t0007g0048 | 2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.325+12831C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44375527 | ||||||
| chr5:44375716
|
GTGATAGT others(4): Show |
G | 1 | a0001c0001t0007g0291 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.325+12631_325+1264 others(15): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44375716 | ||||||
| chr5:44376091
|
A | G | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+12267T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376091 | ||||||
| chr5:44376120
|
C | T | 23 | a0001c0001t0003g0108a0001c0001t0008g0003a0001c0001t0008g0095others(20): Show | 25 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.325+12238G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376120 | ||||||
| chr5:44376331
|
G | T | 1 | a0001c0001t0003g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.325+12027C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376331 | ||||||
| chr5:44376343
|
G | A | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+12015C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376343 | ||||||
| chr5:44376366
|
C | A | 1 | a0003c0004t0038g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.325+11992G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376366 | ||||||
| chr5:44376490
|
C | CA | 22 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0077others(19): Show | 22 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.325+11867dupT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAA | 27 | a0001c0001t0003g0137a0001c0001t0003g0138a0001c0001t0003g0229others(24): Show | 27 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+11865_325+1186 others(7): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAA | 81 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(78): Show | 83 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.325+11864_325+1186 others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAA | 50 | a0001c0001t0001g0212a0001c0001t0002g0031a0001c0001t0002g0036others(47): Show | 50 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.325+11863_325+1186 others(9): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAA | 6 | a0001c0001t0002g0213a0001c0001t0002g0221a0001c0001t0006g0214others(3): Show | 6 | HG01074.hp1 HG01109.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.325+11862_325+1186 others(10): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.325+11856_325+1186 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0297a0001c0001t0002g0320a0001c0001t0017g0295others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+11855_325+1186 others(17): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(7): Show |
17 | a0001c0001t0001g0007a0001c0001t0001g0244a0001c0001t0001g0245others(14): Show | 18 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.325+11854_325+1186 others(18): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(8): Show |
15 | a0001c0001t0001g0008a0001c0001t0001g0246a0001c0001t0001g0289others(12): Show | 16 | HG00544.hp1 HG00741.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.325+11853_325+1186 others(19): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(9): Show |
12 | a0001c0001t0001g0309a0001c0001t0001g0313a0001c0001t0001g0330others(9): Show | 12 | HG00597.hp2 HG03017.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.325+11852_325+1186 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0314a0001c0001t0001g0334 | 2 | HG03239.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.325+11851_325+1186 others(21): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0315a0001c0001t0005g0337 | 4 | HG02040.hp2 HG02738.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+11850_325+1186 others(22): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
CA | C | 13 | a0001c0001t0004g0043a0001c0001t0004g0059a0001c0001t0005g0044others(10): Show | 14 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.325+11867delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0008g0100a0001c0001t0008g0101 | 2 | HG01258.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.325+11858_325+1186 others(14): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0008g0003a0001c0001t0008g0095a0001c0001t0008g0096others(3): Show | 7 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+11857_325+1186 others(15): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376490
|
CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0003g0108a0001c0001t0013g0112a0001c0001t0013g0113others(12): Show | 16 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.325+11856_325+1186 others(16): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376490 | ||||||
| chr5:44376502
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0292 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.325+11840_325+1185 others(20): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376502 | ||||||
| chr5:44376507
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0293 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.325+11840_325+1185 others(15): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376507 | ||||||
| chr5:44376509
|
A | C | 5 | a0001c0001t0006g0238a0001c0001t0012g0025a0001c0001t0012g0026others(2): Show | 5 | HG02615.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.325+11849T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376509 | ||||||
| chr5:44376512
|
A | C | 4 | a0001c0001t0018g0103a0001c0001t0018g0105a0001c0001t0018g0106others(1): Show | 4 | HG01192.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+11846T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376512 | ||||||
| chr5:44376516
|
A | C | 2 | a0001c0001t0010g0251a0001c0001t0032g0252 | 2 | NA19006.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325+11842T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376516 | ||||||
| chr5:44376518
|
C | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 79 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.325+11840G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376518 | ||||||
| chr5:44376597
|
C | T | 3 | a0001c0001t0005g0290a0001c0001t0005g0336a0001c0001t0005g0337 | 3 | HG02738.hp2 HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.325+11761G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376597 | ||||||
| chr5:44376958
|
G | A | 228 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(225): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.325+11400C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376958 | ||||||
| chr5:44376961
|
A | T | 1 | a0001c0001t0002g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.325+11397T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376961 | ||||||
| chr5:44376981
|
G | T | 340 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(337): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.325+11377C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376981 | ||||||
| chr5:44377150
|
G | C | 1 | a0001c0001t0001g0335 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.325+11208C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377150 | ||||||
| chr5:44377439
|
G | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | NA18965.hp2 NA19012.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.325+10919C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377439 | ||||||
| chr5:44377538
|
G | A | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.325+10820C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377538 | ||||||
| chr5:44377544
|
C | T | 2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | NA18943.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.325+10814G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377544 | ||||||
| chr5:44377695
|
G | T | 1 | a0001c0001t0026g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325+10663C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377695 | ||||||
| chr5:44377800
|
C | T | 1 | a0001c0001t0017g0316 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.325+10558G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377800 | ||||||
| chr5:44377863
|
G | T | 5 | a0001c0001t0005g0041a0001c0001t0005g0093a0001c0001t0025g0002others(2): Show | 6 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+10495C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377863 | ||||||
| chr5:44377896
|
T | C | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+10462A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377896 | ||||||
| chr5:44377900
|
A | G | 6 | a0001c0001t0012g0001a0001c0001t0012g0025a0001c0001t0012g0026others(3): Show | 7 | HG01106.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+10458T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44377900 | ||||||
| chr5:44378004
|
A | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 67 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.325+10354T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378004 | ||||||
| chr5:44378079
|
AT | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.325+10278delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378079 | ||||||
| chr5:44378524
|
C | T | 3 | a0001c0001t0020g0239a0001c0001t0020g0240a0001c0001t0020g0241 | 3 | HG02451.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.325+9834G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378524 | ||||||
| chr5:44378588
|
C | T | 1 | a0001c0001t0006g0124 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.325+9770G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378588 | ||||||
| chr5:44378633
|
G | C | 1 | a0001c0001t0006g0124 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.325+9725C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378633 | ||||||
| chr5:44378656
|
C | T | 1 | a0001c0001t0010g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.325+9702G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44378656 | ||||||
| chr5:44379124
|
G | A | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+9234C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379124 | ||||||
| chr5:44379132
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.325+9226A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379132 | ||||||
| chr5:44379202
|
T | C | 2 | a0001c0001t0007g0060a0001c0001t0059g0061 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.325+9156A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379202 | ||||||
| chr5:44379314
|
A | G | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+9044T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379314 | ||||||
| chr5:44379374
|
G | A | 2 | a0001c0001t0014g0088a0001c0001t0014g0089 | 2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.325+8984C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379374 | ||||||
| chr5:44379473
|
C | T | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.325+8885G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379473 | ||||||
| chr5:44379731
|
T | G | 2 | a0001c0001t0030g0120a0001c0001t0031g0037 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.325+8627A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379731 | ||||||
| chr5:44379753
|
G | A | 2 | a0001c0001t0026g0247a0001c0001t0026g0248 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.325+8605C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379753 | ||||||
| chr5:44379834
|
C | G | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.325+8524G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379834 | ||||||
| chr5:44379947
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325+8411G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44379947 | ||||||
| chr5:44380104
|
G | T | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.325+8254C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380104 | ||||||
| chr5:44380117
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325+8241A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380117 | ||||||
| chr5:44380220
|
C | A | 1 | a0001c0001t0002g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.325+8138G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380220 | ||||||
| chr5:44380434
|
C | A | 3 | a0001c0001t0039g0222a0001c0001t0039g0224a0001c0001t0040g0223 | 3 | NA18948.hp2 NA18977.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.325+7924G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380434 | ||||||
| chr5:44380778
|
T | G | 1 | a0001c0001t0005g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.325+7580A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380778 | ||||||
| chr5:44380815
|
T | C | 1 | a0001c0001t0064g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+7543A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380815 | ||||||
| chr5:44380879
|
A | C | 4 | a0001c0001t0002g0128a0001c0001t0015g0125a0001c0001t0015g0126others(1): Show | 4 | HG01099.hp2 HG01123.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+7479T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380879 | ||||||
| chr5:44380907
|
CAGGTTG | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0055g0228 | 3 | HG01167.hp1 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.325+7445_325+7450d others(8): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44380907 | ||||||
| chr5:44381004
|
A | C | 1 | a0001c0001t0001g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.325+7354T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381004 | ||||||
| chr5:44381185
|
T | G | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | NA18950.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.325+7173A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381185 | ||||||
| chr5:44381367
|
G | A | 1 | a0001c0001t0076g0341 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.325+6991C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381367 | ||||||
| chr5:44381470
|
T | TA | 7 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0006g0227others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+6887dupT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381470 | ||||||
| chr5:44381480
|
A | AC | 29 | a0001c0001t0006g0124a0001c0001t0010g0251a0001c0001t0010g0253others(26): Show | 29 | HG00639.hp2 HG00673.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.325+6877_325+6878i others(3): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381480 | ||||||
| chr5:44381480
|
A | C | 1 | a0001c0001t0052g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+6878T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381480 | ||||||
| chr5:44381488
|
C | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 26 | HG01943.hp1 HG01981.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.325+6870G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381488 | ||||||
| chr5:44381511
|
T | C | 1 | a0001c0001t0004g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.325+6847A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381511 | ||||||
| chr5:44381596
|
T | G | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 80 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.325+6762A>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381596 | ||||||
| chr5:44381722
|
C | T | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+6636G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381722 | ||||||
| chr5:44381959
|
C | A | 334 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(331): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.325+6399G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381959 | ||||||
| chr5:44382239
|
T | C | 32 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(29): Show | 32 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.325+6119A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382239 | ||||||
| chr5:44382384
|
T | C | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.325+5974A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382384 | ||||||
| chr5:44382528
|
G | A | 1 | a0001c0001t0005g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.325+5830C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382528 | ||||||
| chr5:44382563
|
T | A | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.325+5795A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382563 | ||||||
| chr5:44382599
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.325+5759C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382599 | ||||||
| chr5:44382703
|
A | C | 5 | a0001c0001t0020g0239a0001c0001t0020g0240a0001c0001t0020g0241others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.325+5655T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382703 | ||||||
| chr5:44382740
|
C | A | 156 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(153): Show | 160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.325+5618G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382740 | ||||||
| chr5:44382794
|
T | C | 25 | a0001c0001t0010g0253a0001c0001t0010g0258a0001c0001t0010g0260others(22): Show | 25 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.325+5564A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382794 | ||||||
| chr5:44382832
|
G | A | 2 | a0001c0001t0005g0336a0001c0001t0005g0337 | 2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.325+5526C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382832 | ||||||
| chr5:44383013
|
G | A | 1 | a0001c0001t0005g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325+5345C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383013 | ||||||
| chr5:44383118
|
CA | C | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+5239delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383118 | ||||||
| chr5:44383170
|
T | A | 15 | a0001c0001t0003g0108a0001c0001t0013g0112a0001c0001t0013g0113others(12): Show | 16 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.325+5188A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383170 | ||||||
| chr5:44383200
|
G | C | 1 | a0001c0001t0037g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.325+5158C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383200 | ||||||
| chr5:44383260
|
C | T | 5 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0001t0004g0285others(2): Show | 5 | HG02723.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.325+5098G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383260 | ||||||
| chr5:44383283
|
GA | G | 62 | a0001c0001t0004g0043a0001c0001t0004g0051a0001c0001t0004g0056others(59): Show | 63 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.325+5074delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383283 | ||||||
| chr5:44383760
|
G | A | 1 | a0001c0001t0009g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.325+4598C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383760 | ||||||
| chr5:44383834
|
G | A | 10 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(7): Show | 10 | HG01192.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.325+4524C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383834 | ||||||
| chr5:44383898
|
G | A | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+4460C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383898 | ||||||
| chr5:44383945
|
C | G | 10 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(7): Show | 10 | HG01192.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.325+4413G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383945 | ||||||
| chr5:44383963
|
C | G | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+4395G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44383963 | ||||||
| chr5:44384054
|
T | C | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+4304A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384054 | ||||||
| chr5:44384081
|
C | T | 225 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(222): Show | 230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.325+4277G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384081 | ||||||
| chr5:44384121
|
C | T | 9 | a0001c0001t0024g0121a0001c0001t0024g0338a0001c0001t0024g0339others(6): Show | 9 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+4237G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384121 | ||||||
| chr5:44384355
|
T | C | 2 | a0001c0001t0028g0249a0001c0001t0028g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.325+4003A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384355 | ||||||
| chr5:44384779
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325+3579A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384779 | ||||||
| chr5:44384840
|
T | C | 1 | a0001c0001t0011g0277 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.325+3518A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384840 | ||||||
| chr5:44384867
|
A | G | 2 | a0001c0001t0030g0120a0001c0001t0031g0037 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.325+3491T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44384867 | ||||||
| chr5:44385224
|
C | G | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+3134G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385224 | ||||||
| chr5:44385293
|
T | C | 27 | a0001c0001t0010g0251a0001c0001t0010g0253a0001c0001t0010g0258others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.325+3065A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385293 | ||||||
| chr5:44385313
|
G | A | 132 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(129): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.325+3045C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385313 | ||||||
| chr5:44385336
|
C | T | 2 | a0001c0001t0005g0039a0002c0003t0050g0030 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.325+3022G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385336 | ||||||
| chr5:44385402
|
G | T | 1 | a0001c0001t0003g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.325+2956C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385402 | ||||||
| chr5:44385995
|
T | C | 1 | a0001c0001t0006g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.325+2363A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44385995 | ||||||
| chr5:44386555
|
A | T | 1 | a0001c0001t0031g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325+1803T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44386555 | ||||||
| chr5:44386716
|
T | C | 3 | a0001c0001t0026g0278a0001c0001t0073g0279a0001c0001t0075g0280 | 3 | HG01346.hp1 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.325+1642A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44386716 | ||||||
| chr5:44386748
|
G | A | 331 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(328): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.325+1610C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44386748 | ||||||
| chr5:44386840
|
C | A | 1 | a0001c0001t0007g0235 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.325+1518G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44386840 | ||||||
| chr5:44386882
|
A | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(1): Show | 4 | NA18972.hp1 NA19005.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+1476T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44386882 | ||||||
| chr5:44387054
|
C | T | 1 | a0002c0003t0050g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325+1304G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387054 | ||||||
| chr5:44387241
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0006g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.325+1117C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387241 | ||||||
| chr5:44387242
|
G | T | 2 | a0001c0001t0002g0031a0001c0001t0006g0032 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.325+1116C>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387242 | ||||||
| chr5:44387435
|
A | C | 228 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0180others(225): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.325+923T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387435 | ||||||
| chr5:44387741
|
C | CCAAAA | 9 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0018others(6): Show | 9 | HG01192.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.325+612_325+616dup others(5): Show |
FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387741 | ||||||
| chr5:44388048
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 64 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.325+310C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44388048 | ||||||
| chr5:44388079
|
G | C | 2 | a0001c0001t0024g0338a0001c0001t0024g0339 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.325+279C>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44388079 | ||||||
| chr5:44388206
|
G | A | 1 | a0001c0001t0072g0340 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.325+152C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44388206 |