Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MWKWI others(203): Show |
chr5 | 44295247 | 44394420 |
| a0002 | 0/0 | 208 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | MWKWI others(203): Show |
chr5 | 44295247 | 44394420 |
| a0003 | 0/0 | 208 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | MWKWI others(203): Show |
chr5 | 44295247 | 44394420 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 624 | 342 | 80 | 60 | 158 | 14 | 28 | FGF10_chr5_44295247_44394420 | FGF10 | ATGTG others(619): Show |
chr5 | 44295247 | 44394420 | ||
| a0001c0002 | 0/0 | 624 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | ATGTG others(619): Show |
chr5 | 44295247 | 44394420 | ||
| a0002c0004 | 0/0 | 624 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | ATGTG others(619): Show |
chr5 | 44295247 | 44394420 | ||
| a0003c0003 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | ATGTG others(619): Show |
chr5 | 44295247 | 44394420 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6113 | 102 | 2 | 21 | 63 | 7 | 9 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0002 | 0/0 | 6113 | 60 | 24 | 2 | 30 | 0 | 4 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0003 | 0/0 | 6114 | 59 | 6 | 12 | 34 | 2 | 5 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0004 | 0/0 | 6113 | 20 | 0 | 2 | 18 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0005 | 0/0 | 6114 | 10 | 4 | 2 | 0 | 2 | 2 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0006 | 0/0 | 6113 | 9 | 0 | 6 | 0 | 1 | 2 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0007 | 0/0 | 6112 | 8 | 7 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6107): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0008 | 0/0 | 6114 | 7 | 6 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0009 | 0/0 | 6109 | 5 | 4 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6104): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0010 | 0/0 | 6088 | 4 | 4 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6083): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0011 | 0/0 | 6112 | 4 | 0 | 4 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6107): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0012 | 0/0 | 6113 | 4 | 0 | 0 | 4 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0013 | 0/0 | 6113 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0014 | 0/0 | 6112 | 3 | 0 | 0 | 0 | 0 | 3 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6107): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0015 | 0/0 | 6100 | 3 | 3 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6095): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0016 | 0/0 | 6113 | 3 | 0 | 2 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0017 | 0/0 | 6112 | 2 | 0 | 1 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6107): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0018 | 0/0 | 6114 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0019 | 1/0 | 6113 | 2 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0020 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0021 | 0/0 | 6145 | 2 | 0 | 0 | 1 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6140): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0022 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0023 | 0/0 | 6149 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6144): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0024 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0025 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6095): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0026 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0027 | 0/0 | 6112 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6107): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0028 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6103): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0029 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0030 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0031 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0033 | 0/1 | 6109 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6104): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0034 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6100): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0035 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0036 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0037 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0038 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0039 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0040 | 0/0 | 6153 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6148): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0041 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0042 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0043 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0044 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0045 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0046 | 0/0 | 6109 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6104): Show |
chr5 | 44295247 | 44394420 |
| a0001c0001t0047 | 0/0 | 6114 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6109): Show |
chr5 | 44295247 | 44394420 |
| a0001c0002t0002 | 0/0 | 6113 | 6 | 5 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0002c0004t0002 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| a0003c0003t0032 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | GACAT others(6108): Show |
chr5 | 44295247 | 44394420 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0011g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0015g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0017g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0018g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0019g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0021g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0021g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0022g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0023g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0023g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0024g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0025g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0027g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0028g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0029g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0030g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0031g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0033g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0034g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0035g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0036g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0037g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0038g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0039g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0040g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0041g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0042g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0043g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0044g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0045g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0046g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0001t0047g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0002c0004t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| a0003c0003t0032g0045 | 0/0 | 1 | 1 | 0 | 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 | t0003 | g0278 | EUR | GBR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0093 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0055 | EUR | FIN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0120 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0096 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01070 | hp1 | a0001 | c0001 | t0011 | g0119 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01099 | hp1 | a0001 | c0001 | t0047 | g0313 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01109 | hp2 | a0001 | c0001 | t0046 | g0106 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01168 | hp1 | a0001 | c0001 | t0016 | g0010 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01169 | hp2 | a0001 | c0001 | t0016 | g0010 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01175 | hp1 | a0002 | c0004 | t0002 | g0077 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01175 | hp2 | a0001 | c0001 | t0017 | g0032 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0101 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01257 | hp1 | a0001 | c0001 | t0023 | g0236 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0310 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0099 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0311 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0255 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01358 | hp2 | a0001 | c0001 | t0023 | g0247 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01361 | hp1 | a0001 | c0001 | t0025 | g0031 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01515 | hp1 | a0001 | c0001 | t0017 | g0028 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0015 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0015 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01884 | hp1 | a0003 | c0003 | t0032 | g0045 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0073 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02055 | hp1 | a0001 | c0001 | t0042 | g0069 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | CDX | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0065 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0034 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0254 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0218 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02523 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | KHV | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0118 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02622 | hp1 | a0001 | c0001 | t0024 | g0107 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0098 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02717 | hp2 | a0001 | c0001 | t0026 | g0030 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0220 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02818 | hp2 | a0001 | c0001 | t0038 | g0184 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02895 | hp2 | a0001 | c0001 | t0037 | g0112 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0219 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0102 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0169 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0253 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0129 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03130 | hp1 | a0001 | c0001 | t0039 | g0100 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0121 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03486 | hp1 | a0001 | c0001 | t0020 | g0133 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03491 | hp1 | a0001 | c0001 | t0014 | g0167 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ESN | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03540 | hp1 | a0001 | c0001 | t0034 | g0209 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03579 | hp1 | a0001 | c0001 | t0043 | g0068 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0164 | SAS | PJL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03831 | hp1 | a0001 | c0001 | t0045 | g0312 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04115 | hp1 | a0001 | c0001 | t0014 | g0142 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04115 | hp2 | a0001 | c0001 | t0027 | g0029 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18522 | hp1 | a0001 | c0001 | t0036 | g0170 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18747 | hp2 | a0001 | c0001 | t0040 | g0242 | EAS | CHB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0221 | AFR | YRI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18943 | hp2 | a0001 | c0001 | t0044 | g0085 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0203 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18950 | hp2 | a0001 | c0001 | t0022 | g0024 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18964 | hp2 | a0001 | c0001 | t0022 | g0024 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18969 | hp2 | a0001 | c0001 | t0035 | g0292 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18977 | hp2 | a0001 | c0001 | t0012 | g0204 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18994 | hp2 | a0001 | c0001 | t0021 | g0251 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0205 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19004 | hp2 | a0001 | c0001 | t0030 | g0234 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19030 | hp2 | a0001 | c0001 | t0019 | g0052 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0228 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19063 | hp1 | a0001 | c0001 | t0031 | g0144 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19067 | hp1 | a0001 | c0001 | t0041 | g0284 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20129 | hp1 | a0001 | c0001 | t0029 | g0040 | AFR | ASW | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ASW | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0286 | EUR | TSI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0095 | SAS | GIH | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20905 | hp2 | a0001 | c0001 | t0021 | g0231 | SAS | GIH | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0094 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0226 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02486 | hp2 | a0001 | c0001 | t0015 | g0173 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0111 | AFR | MSL | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0197 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | USA | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0229 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | LWK | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0033 | g0126 | REF | REF | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0019 | g0215 | REF | REF | FGF10_chr5_44295247_44394420 | FGF10 | chr5 | 44295247 | 44394420 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44305002 | T | G | 1 | a0002 | 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 | a0003 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44300259 | T | TTC | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(19): 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 | a0001c0001t0043 | 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 | a0001c0001t0022 | 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 | a0001c0001t0029 | 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 | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(4): 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 | 11 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(8): 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 | a0001c0001t0046 | 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 | a0001c0001t0038 | 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 | a0001c0001t0035 | 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 | a0001c0001t0039 | 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 | 2 | a0001c0001t0006 a0001c0001t0018 |
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 | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0044 | 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 | 3 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0027 |
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 | a0001c0001t0037 | 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 | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(4): 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 | 1 | a0001c0001t0006 | 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 | 6 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0015 others(3): 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 | a0001c0001t0020 | 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 | a0001c0001t0038 | 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 | a0001c0001t0016 | 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 | 4 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0031 others(1): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): 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 | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0015 others(1): 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 | a0001c0001t0023 | 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 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0034 |
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 | a0001c0001t0010 | 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 | a0001c0001t0002 a0002c0004t0002 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 |
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 | a0001c0001t0001 a0003c0003t0032 |
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 | a0001c0001t0004 | 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 | a0001c0001t0004 a0001c0001t0022 |
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 | a0001c0001t0004 a0001c0001t0030 |
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 | a0001c0001t0004 | 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(9): Show |
72 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(69): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(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 | a0001c0001t0003 | 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 | a0001c0001t0039 | 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 | a0001c0001t0003 | 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 | a0001c0001t0047 | 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 | a0001c0001t0040 | 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 | a0001c0001t0021 | 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 | 1 | a0001c0001t0012 | 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 | a0001c0001t0042 | 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 | 3 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0027 |
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 | a0001c0001t0027 | 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 | a0001c0001t0039 | 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 | a0001c0001t0039 | 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 | 4 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0041 others(1): 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 | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(30): 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 | 1 | a0001c0001t0006 | 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 | a0001c0001t0039 | 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 | 6 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0022 others(3): 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 | a0003c0003t0032 | 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 | a0001c0001t0018 | 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 | a0001c0001t0045 | 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 | a0001c0001t0041 | 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 | 3 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0046 |
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 | a0001c0001t0031 | 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 | 5 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0024 others(2): 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 | 10 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(7): 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 | a0001c0001t0030 | 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 | 3 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0046 |
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 | 2 | a0001c0001t0008 a0001c0001t0029 |
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 | 2 | a0001c0001t0007 a0001c0001t0028 |
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 | a0001c0001t0047 | 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 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0026 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:44305204 | A | AAACAGAA others(5): Show |
1 | a0001c0001t0002g0259 | 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 | 55 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(52): 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 | a0001c0001t0003g0291 | 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 | a0001c0001t0001g0212 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 70 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(67): 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 | a0001c0001t0004g0252 | 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 | a0001c0001t0004g0238 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0002t0002g0064 a0001c0002t0002g0065 a0001c0002t0002g0222 |
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 | 102 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(99): 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0003g0283 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 7 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(4): 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 | a0001c0001t0005g0113 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0001g0149 | 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 | a0001c0002t0002g0064 a0001c0002t0002g0065 a0001c0002t0002g0222 |
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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 80 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(77): 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 | a0001c0001t0002g0308 a0001c0001t0002g0309 |
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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 7 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(4): 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 | 53 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(50): 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 | a0001c0001t0024g0107 a0001c0001t0024g0169 a0001c0001t0026g0030 |
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 | a0001c0001t0004g0232 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0101 a0001c0001t0005g0102 others(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 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0003g0276 | 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 | a0001c0001t0028g0034 | 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 | a0001c0001t0001g0213 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0013g0197 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0003g0272 | 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 | a0001c0001t0003g0272 | 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 | 59 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(56): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0008g0042 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0005g0102 | 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 | a0001c0001t0001g0177 | 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 | 70 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(67): 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 | 51 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0025 others(48): 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0025g0031 |
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 | 8 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): 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 | a0001c0001t0008g0041 | 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 | a0001c0001t0002g0054 | 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 | 71 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(68): 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 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0221 others(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 | a0001c0001t0005g0076 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 81 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(78): 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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0132 | 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 | 96 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(93): 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0005g0110 a0001c0001t0005g0113 |
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 | a0001c0001t0009g0255 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0004g0233 | 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 115 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(112): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0001g0165 a0001c0001t0001g0192 a0001c0001t0020g0129 others(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 | 145 | a0001c0001t0001g0103 a0001c0001t0001g0179 a0001c0001t0002g0001 others(142): 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0013g0118 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0003g0267 | 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 | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0003c0003t0032g0045 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0003g0289 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0001c0001t0036g0170 | 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 | 188 | a0001c0001t0001g0103 a0001c0001t0002g0001 a0001c0001t0002g0003 others(185): 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0221 others(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 | 65 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(62): 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 | 71 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(68): 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 | 110 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(107): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.326-3059dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44313588 | |||||||
| chr5:44313588 | G | GTT | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | 67 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(64): 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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(22): 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 | a0001c0001t0004g0239 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0071 a0001c0001t0002g0072 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0002g0091 a0001c0001t0045g0312 |
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 | 81 | a0001c0001t0001g0103 a0001c0001t0003g0006 a0001c0001t0003g0008 others(78): 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 | a0001c0001t0043g0068 | 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 | a0001c0001t0007g0036 a0001c0001t0007g0038 |
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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | 137 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(134): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.326-4653delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315182 | |||||||
| chr5:44315182 | CAA | C | 107 | a0001c0001t0001g0103 a0001c0001t0001g0127 a0001c0001t0002g0001 others(104): 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 | a0001c0001t0002g0260 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0011g0119 a0001c0001t0011g0120 a0001c0001t0011g0310 others(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 | a0001c0001t0005g0101 a0001c0001t0005g0111 a0001c0001t0005g0114 others(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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.326-5111A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44315641 | |||||||
| chr5:44315705 | C | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0002t0002g0064 | 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 | a0001c0001t0003g0264 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0003g0270 a0001c0001t0003g0271 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0004g0248 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0017g0028 | 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 | a0001c0001t0003g0268 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | a0001c0001t0005g0076 | 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 | a0001c0001t0013g0121 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0001g0152 others(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 | a0001c0001t0018g0228 a0001c0001t0018g0229 a0001c0001t0038g0184 |
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 | a0003c0003t0032g0045 | 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 | 4 | a0001c0001t0008g0002 a0001c0001t0008g0041 a0001c0001t0008g0042 others(1): 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 | 24 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0232 others(21): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0005g0110 | 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 | a0001c0001t0020g0129 a0001c0001t0020g0133 |
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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | 169 | a0001c0001t0001g0103 a0001c0001t0002g0001 a0001c0001t0002g0003 others(166): 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 | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0254 |
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 | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0003g0280 | 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 | 1 | a0001c0001t0003g0006 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0012g0203 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 1 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
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 | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0003g0270 a0001c0001t0003g0271 |
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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.326-10183delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44320712 | |||||||
| chr5:44320866 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(63): 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 | 31 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0232 others(28): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0003g0268 a0001c0001t0003g0280 a0001c0001t0003g0282 others(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 | 65 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(62): 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 | a0001c0001t0035g0292 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 64 | a0001c0001t0001g0022 a0001c0001t0002g0001 a0001c0001t0002g0003 others(61): 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 | a0001c0001t0003g0283 | 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 | 8 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): 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 | a0001c0001t0005g0076 | 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 | 24 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0232 others(21): 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0006g0094 a0001c0001t0006g0099 |
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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | 58 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(55): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0005g0111 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
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 | a0001c0001t0002g0054 a0001c0001t0002g0070 |
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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0003g0283 | 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 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0084 |
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 | a0001c0001t0001g0180 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0002g0058 a0001c0001t0002g0074 |
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 | a0001c0001t0003g0027 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0002g0258 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0023g0236 | 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 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
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 | 106 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(103): 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 | 117 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(114): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.326-14837A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44325367 | |||||||
| chr5:44325405 | C | A | 169 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(166): 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 | 58 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(55): 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0037g0112 | 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 | 177 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(174): 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 | a0001c0001t0003g0274 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0013g0121 | 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 | a0001c0001t0037g0112 | 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 | 90 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | 58 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(55): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0003g0267 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0048 others(5): 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 | a0001c0001t0002g0256 | 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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | a0001c0001t0003g0305 | 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 | 8 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0066 others(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 | 304 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(301): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.326-17617T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328147 | |||||||
| chr5:44328168 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(144): 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 | a0001c0001t0039g0100 | 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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(144): 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 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0225 |
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 | 304 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(301): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.326-17921G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44328451 | |||||||
| chr5:44328464 | A | T | 1 | a0001c0001t0003g0006 | 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 141 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(138): 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 | a0001c0001t0001g0148 a0001c0001t0001g0208 |
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 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(144): 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 | a0001c0001t0004g0240 a0001c0001t0004g0252 |
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 | a0001c0001t0020g0133 | 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 | 297 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(294): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0002g0063 | 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 | 141 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(138): 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0002g0048 | 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 | a0001c0001t0005g0101 | 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 | a0001c0002t0002g0064 a0001c0002t0002g0065 a0001c0002t0002g0067 others(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 | a0001c0001t0005g0015 | 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 | 3 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0083 |
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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0004g0241 | 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-20199C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330729 | |||||||
| chr5:44330755 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(37): 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 | a0001c0001t0002g0054 a0001c0001t0002g0056 a0001c0001t0002g0059 others(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 | a0001c0001t0011g0119 | 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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.326-20363T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44330893 | |||||||
| chr5:44330944 | C | A | 1 | a0001c0001t0022g0024 | 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 | a0001c0001t0047g0313 | 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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0048 others(4): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0013g0121 | 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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(144): 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 | a0001c0001t0001g0199 | 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 | 6 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(3): 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 | a0001c0001t0001g0152 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0003g0109 | 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 | a0001c0001t0002g0060 | 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 | a0001c0001t0004g0250 | 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 | a0001c0001t0020g0129 a0001c0001t0020g0133 |
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 | a0001c0001t0013g0118 | 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0004g0250 | 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 | a0001c0001t0015g0221 | 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 | a0001c0001t0036g0170 | 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 | a0001c0001t0002g0265 a0001c0001t0002g0308 a0001c0001t0002g0309 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 100 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(97): 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0011g0119 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0006g0098 | 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 | a0001c0001t0002g0216 a0001c0001t0010g0073 a0001c0001t0010g0218 others(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 | 69 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(66): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0145 | 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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0071 a0001c0001t0002g0072 others(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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0004g0243 a0001c0001t0004g0245 |
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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-24351T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334881 | |||||||
| chr5:44334910 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326-24380G>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44334910 | |||||||
| chr5:44334912 | G | A | 22 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(19): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0003g0263 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0150 | 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 | 121 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): 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 | a0002c0004t0002g0077 | 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 | a0001c0001t0003g0299 | 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 | a0001c0001t0005g0101 a0001c0001t0005g0111 a0001c0001t0005g0114 others(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 | a0001c0001t0013g0118 | 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 | 10 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(7): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0027g0029 | 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 | a0001c0001t0016g0055 | 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 | a0001c0001t0024g0107 a0001c0001t0024g0169 |
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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0102 others(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 | a0001c0001t0001g0193 a0001c0001t0006g0014 a0001c0001t0006g0093 others(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 | 68 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(65): 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.326-26733delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337262 | |||||||
| chr5:44337536 | A | C | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-27006T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44337536 | |||||||
| chr5:44337588 | C | T | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0003g0271 | 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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0019g0052 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | a0001c0001t0002g0054 | 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 | 97 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(94): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 27 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(24): 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 | 10 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(7): 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 | a0001c0001t0040g0242 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 119 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(116): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.326-29178C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44339708 | |||||||
| chr5:44339882 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(115): Show |
130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): 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 | a0001c0001t0001g0018 a0001c0001t0001g0140 a0001c0001t0001g0183 |
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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 117 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(114): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): 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 | a0001c0001t0013g0121 | 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 | a0001c0001t0002g0216 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0005g0101 a0001c0001t0005g0110 a0001c0001t0005g0111 others(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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | a0001c0002t0002g0064 a0001c0002t0002g0065 a0001c0002t0002g0067 others(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 | a0001c0001t0002g0260 | 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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326-30295A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44340825 | |||||||
| chr5:44340873 | T | G | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0027g0029 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0013g0121 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0028g0034 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(61): 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 | a0001c0001t0002g0266 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0013g0197 | 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 | a0001c0001t0019g0052 | 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 | a0001c0001t0036g0170 | 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 | 261 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): 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 | a0001c0001t0001g0018 a0001c0001t0001g0140 a0001c0001t0001g0183 |
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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.326-31347T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44341877 | |||||||
| chr5:44342070 | A | G | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0004g0250 | 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 | 120 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(117): 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 | a0001c0001t0003g0297 | 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 | a0001c0001t0002g0061 | 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 | 8 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0020g0129 a0001c0001t0020g0133 |
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 | a0001c0001t0003g0270 a0001c0001t0003g0271 |
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 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 others(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 | a0001c0001t0036g0170 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | a0001c0001t0007g0036 | 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 | a0001c0001t0001g0022 | 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 |
9 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(6): 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 | a0001c0001t0002g0071 a0001c0001t0013g0121 |
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 | a0001c0001t0001g0202 | 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 | 52 | a0001c0001t0001g0053 a0001c0001t0001g0293 a0001c0001t0001g0296 others(49): 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 | a0001c0001t0002g0004 a0001c0001t0003g0025 a0001c0001t0003g0223 others(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 |
17 | a0001c0001t0001g0103 a0001c0001t0001g0132 a0001c0001t0002g0001 others(14): 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 |
17 | a0001c0001t0001g0148 a0001c0001t0001g0208 a0001c0001t0002g0004 others(14): 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 |
42 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(39): Show |
44 | HG00438.hp1 HG00673.hp2 HG01123.hp1 others(41): 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 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0122 others(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 |
44 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(41): 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 |
15 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0046 others(12): 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 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0176 others(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 | a0001c0001t0020g0129 | 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 | 30 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(27): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | a0001c0001t0009g0255 | 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 | a0001c0001t0002g0001 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0005g0076 | 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0003g0269 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 |
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 | a0001c0001t0005g0076 | 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 | a0001c0001t0002g0216 a0001c0001t0004g0230 a0001c0001t0004g0243 others(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 | 132 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(129): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.326-35104delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44345633 | |||||||
| chr5:44345633 | CAA | C | 62 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0003 others(59): 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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0005g0015 a0001c0001t0005g0104 |
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 | a0001c0001t0013g0121 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0002t0002g0067 | 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 | a0001c0001t0019g0052 | 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 | a0002c0004t0002g0077 | 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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0013g0121 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0013g0121 | 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 | a0001c0001t0001g0149 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0225 others(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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | 105 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(102): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(112): 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | a0001c0001t0011g0119 a0001c0001t0011g0120 a0001c0001t0011g0310 others(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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0003g0301 a0001c0001t0003g0305 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0038g0184 | 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 | a0001c0001t0001g0127 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0001g0195 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0002g0070 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0200 | 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 | 119 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(116): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0002g0062 a0001c0001t0002g0259 |
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 | a0001c0001t0004g0237 a0001c0001t0004g0240 a0001c0001t0004g0248 others(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 | a0001c0001t0004g0241 a0001c0001t0004g0243 a0001c0001t0004g0244 others(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 | a0001c0001t0004g0232 a0001c0001t0022g0024 a0001c0001t0023g0247 others(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 | a0001c0001t0004g0172 a0001c0001t0004g0235 a0001c0001t0004g0238 |
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 | a0001c0001t0021g0231 | 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 | a0001c0001t0021g0251 | 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 | a0001c0001t0008g0002 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0194 | 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 | a0001c0001t0012g0205 | 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 | a0001c0001t0003g0271 | 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 | a0001c0001t0003g0272 | 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 | 1 | a0001c0001t0004g0230 | 1 | NA19006.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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0220 |
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 | a0001c0001t0010g0219 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0002g0056 a0001c0001t0002g0070 a0001c0001t0002g0265 others(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 | a0001c0001t0002g0059 a0001c0001t0002g0257 a0001c0001t0013g0197 |
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 | a0001c0001t0009g0254 | 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 | a0001c0001t0046g0106 | 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 | a0001c0001t0006g0093 | 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 | a0001c0001t0009g0255 | 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 | a0001c0001t0009g0226 | 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 | a0001c0001t0009g0227 | 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 | a0001c0001t0009g0253 | 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 | a0001c0001t0002g0091 | 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 | a0001c0001t0006g0014 | 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 | a0001c0001t0006g0095 a0001c0001t0006g0097 |
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 | a0001c0001t0006g0096 | 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 | a0001c0001t0006g0098 | 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 | a0001c0001t0006g0094 a0001c0001t0006g0099 a0001c0001t0028g0034 |
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 | a0001c0001t0003g0270 | 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 | a0001c0001t0001g0132 a0001c0001t0002g0003 a0001c0001t0002g0066 others(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 | a0001c0001t0005g0015 | 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 | a0001c0001t0037g0112 | 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 | a0001c0001t0001g0103 a0001c0001t0005g0111 |
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 | a0001c0001t0005g0101 a0001c0001t0005g0102 a0001c0001t0005g0114 others(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 | a0001c0001t0005g0104 | 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 | a0001c0001t0003g0008 a0001c0001t0003g0025 a0001c0001t0003g0108 others(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 | a0001c0001t0003g0286 | 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 | a0001c0001t0003g0261 | 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 |
34 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(31): 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 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0025 a0001c0001t0003g0306 |
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 | a0001c0001t0003g0025 a0001c0001t0003g0306 |
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 | a0001c0001t0004g0023 | 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 | a0001c0001t0004g0023 | 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 | 18 | a0001c0001t0001g0046 a0001c0001t0001g0139 a0001c0001t0001g0202 others(15): 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 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0221 others(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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 29 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0019 others(26): 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 | 48 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): 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 | 34 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0131 others(31): 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 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0125 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0208 a0001c0001t0002g0012 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0187 a0001c0001t0002g0001 others(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 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0029g0040 |
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 | 7 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(4): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(72): 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 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
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 | a0001c0001t0013g0118 a0001c0001t0036g0170 |
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 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.325+38669delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44349688 | |||||||
| chr5:44349832 | T | C | 7 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 10 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(7): 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 | a0001c0002t0002g0064 a0001c0002t0002g0065 a0001c0002t0002g0067 others(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 | a0001c0001t0001g0155 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0001g0103 a0001c0001t0005g0015 a0001c0001t0005g0101 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0011g0119 a0001c0001t0011g0120 a0001c0001t0011g0310 others(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 | a0001c0001t0002g0082 | 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 | a0001c0001t0001g0103 | 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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0002g0079 | 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 | a0001c0001t0006g0093 | 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 | a0001c0001t0013g0121 | 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 | a0001c0001t0006g0093 | 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0009g0254 | 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 | a0001c0001t0021g0251 | 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 | a0001c0001t0013g0118 | 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 | a0001c0001t0006g0095 | 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 | a0001c0001t0004g0244 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0003g0278 | 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 | a0001c0001t0013g0118 | 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 | a0001c0001t0034g0209 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0208 |
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 | 182 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(179): Show |
206 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(203): 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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | 261 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): 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 | a0001c0001t0001g0131 a0001c0001t0001g0160 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
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 | a0001c0001t0003g0223 | 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0027g0029 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0018g0228 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0104 |
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 | a0001c0001t0001g0143 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0014g0142 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0002g0075 | 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.325+33097A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44355261 | |||||||
| chr5:44355301 | A | G | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0045g0312 | 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 | 58 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(55): 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 | 2 | a0001c0001t0001g0022 a0001c0001t0034g0209 |
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 | a0001c0001t0004g0230 a0001c0001t0021g0231 |
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 | 303 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(300): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0003g0224 | 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 | a0001c0001t0006g0094 a0001c0001t0006g0099 |
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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.325+32113A>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44356245 | |||||||
| chr5:44356288 | C | T | 310 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(307): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): 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 | a0001c0001t0005g0113 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | a0001c0001t0003g0267 | 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 | 185 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(182): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.325+31239delT | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44357118 | |||||||
| chr5:44357120 | A | T | 1 | a0001c0001t0013g0121 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0003g0278 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0002g0216 a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0038g0184 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0003g0285 a0001c0001t0003g0287 |
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 | a0003c0003t0032g0045 | 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 | 24 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0232 others(21): 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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+29596C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358762 | |||||||
| chr5:44358794 | C | T | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+29564G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44358794 | |||||||
| chr5:44358799 | G | A | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0002g0216 a0001c0001t0009g0226 a0001c0001t0009g0227 others(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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | 15 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0145 others(12): 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 | a0001c0001t0001g0147 | 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 | 44 | a0001c0001t0002g0216 a0001c0001t0004g0023 a0001c0001t0004g0172 others(41): 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0003g0261 a0001c0001t0003g0273 a0001c0001t0003g0274 |
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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0005g0102 | 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 | a0001c0001t0008g0043 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0003g0282 | 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 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0266 |
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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0004g0235 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0159 others(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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | 33 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0049 others(30): 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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0004g0232 a0001c0001t0004g0237 a0001c0001t0023g0236 others(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 | 121 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+25922C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362436 | |||||||
| chr5:44362458 | A | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.325+25900T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362458 | |||||||
| chr5:44362667 | C | T | 121 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+25691G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44362667 | |||||||
| chr5:44362818 | T | C | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(306): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0018g0229 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+25117G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44363241 | |||||||
| chr5:44363475 | A | T | 7 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0048 others(4): 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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0048 others(4): 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0019g0052 | 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 | 183 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0002g0216 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0009g0253 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0003g0261 | 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 | a0001c0001t0015g0174 | 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 | 24 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0232 others(21): 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 | a0001c0001t0003g0267 | 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 | 10 | a0001c0001t0001g0022 a0001c0001t0007g0009 a0001c0001t0007g0033 others(7): 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 | 77 | a0001c0001t0001g0143 a0001c0001t0002g0001 a0001c0001t0002g0003 others(74): 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 | 97 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0017 others(94): Show |
106 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(103): 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 | 18 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): 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 | a0001c0001t0013g0118 | 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.325+22915G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44365443 | |||||||
| chr5:44365531 | C | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): 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 | a0001c0001t0001g0196 | 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 | 310 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(307): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): 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 | a0001c0001t0003g0268 | 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 | a0001c0001t0002g0074 | 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 | 132 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(129): Show |
152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.325+22230dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366127 | |||||||
| chr5:44366127 | C | CTT | 74 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0139 others(71): 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 | 35 | a0001c0001t0002g0266 a0001c0001t0003g0225 a0001c0001t0003g0267 others(32): 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 | a0001c0001t0004g0235 a0001c0001t0006g0014 a0001c0001t0006g0093 others(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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | a0001c0001t0001g0168 | 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 | 78 | a0001c0001t0001g0103 a0001c0001t0001g0293 a0001c0001t0001g0296 others(75): 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 | a0001c0001t0004g0233 | 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 | a0001c0001t0013g0118 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+21618T>C | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366740 | |||||||
| chr5:44366747 | G | A | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+21611C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44366747 | |||||||
| chr5:44367119 | A | T | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0253 others(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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(279): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.325+20514delA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44367843 | |||||||
| chr5:44367843 | GTT | G | 8 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0002g0216 a0001c0001t0010g0073 a0001c0001t0010g0218 others(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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.325+20337C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44368021 | |||||||
| chr5:44368148 | G | T | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(59): 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 | a0001c0001t0001g0103 a0001c0001t0003g0108 a0001c0001t0003g0109 others(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 | 184 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(181): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): 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 | a0003c0003t0032g0045 | 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 | a0003c0003t0032g0045 | 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 | 61 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(58): 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0019g0052 | 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 | a0001c0001t0002g0135 | 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 | 6 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(3): 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0005g0076 | 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 | a0001c0001t0005g0076 | 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 | 119 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(116): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.325+18804G>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44369554 | |||||||
| chr5:44370062 | G | C | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | a0001c0001t0004g0245 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
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 | a0001c0001t0003g0307 | 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 | a0001c0001t0002g0216 a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0002g0216 | 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 | a0001c0001t0002g0216 | 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 | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): 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 | 1 | a0001c0001t0001g0132 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.325+17103C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44371255 | |||||||
| chr5:44371296 | T | C | 253 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(250): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0005g0114 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 1 | a0001c0001t0001g0017 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(250): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0017g0028 | 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 | 112 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(109): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): 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 | a0001c0001t0015g0174 a0001c0001t0025g0031 |
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 | a0001c0001t0003g0283 | 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 | a0001c0001t0001g0138 a0001c0001t0003g0306 |
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 | a0001c0001t0009g0254 | 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 | a0001c0001t0030g0234 | 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 | a0001c0001t0010g0073 a0001c0001t0010g0218 a0001c0001t0010g0219 others(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 | a0001c0001t0001g0137 | 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 | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+15620C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372738 | |||||||
| chr5:44372762 | T | C | 305 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.325+15596A>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44372762 | |||||||
| chr5:44372958 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(91): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0018g0228 | 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 | a0001c0001t0039g0100 | 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 | a0001c0001t0004g0246 | 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 | a0001c0001t0005g0102 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0013g0121 | 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 | 26 | a0001c0001t0004g0023 a0001c0001t0004g0172 a0001c0001t0004g0230 others(23): 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 | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(61): 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0021g0251 | 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 | a0001c0001t0028g0034 | 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 | 191 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(188): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0006g0097 | 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 | 16 | a0001c0001t0002g0061 a0001c0001t0002g0070 a0001c0001t0007g0009 others(13): 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 | a0001c0001t0026g0030 | 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 | 292 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(289): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.325+13472dupA | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44374885 | |||||||
| chr5:44375104 | C | T | 1 | a0001c0001t0003g0272 | 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 | 103 | a0001c0001t0001g0217 a0001c0001t0001g0293 a0001c0001t0001g0296 others(100): 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 | a0001c0001t0026g0030 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
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 | a0001c0001t0002g0266 | 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 | a0003c0003t0032g0045 | 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 | a0001c0001t0001g0103 a0001c0001t0003g0108 a0001c0001t0003g0109 others(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 | a0001c0001t0001g0134 | 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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | a0002c0004t0002g0077 | 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 | 17 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(14): 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 | 24 | a0001c0001t0001g0022 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): Show |
26 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(23): 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 | 75 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): 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 | 45 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0019 others(42): 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 | 5 | a0001c0001t0001g0021 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): 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 | a0001c0001t0003g0261 | 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 | a0001c0001t0001g0293 a0001c0001t0003g0269 a0001c0001t0003g0270 others(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 |
16 | a0001c0001t0001g0296 a0001c0001t0003g0008 a0001c0001t0003g0223 others(13): 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 | a0001c0001t0001g0300 a0001c0001t0002g0259 a0001c0001t0003g0026 others(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 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0308 others(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 | a0001c0001t0003g0288 a0001c0001t0003g0306 |
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 | a0001c0001t0002g0309 a0001c0001t0003g0027 a0001c0001t0003g0289 |
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 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0059 others(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 | a0001c0001t0006g0098 a0001c0001t0006g0099 |
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 | a0001c0001t0006g0014 a0001c0001t0006g0093 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0103 a0001c0001t0003g0108 a0001c0001t0003g0109 others(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 | a0001c0001t0003g0290 | 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 | a0001c0001t0003g0268 | 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 | a0001c0001t0001g0217 a0001c0001t0008g0002 a0001c0001t0008g0041 others(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 | a0001c0001t0005g0101 a0001c0001t0005g0111 a0001c0001t0005g0114 others(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 | a0001c0001t0004g0230 a0001c0001t0021g0231 |
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 | 74 | a0001c0001t0001g0130 a0001c0001t0001g0180 a0001c0001t0001g0200 others(71): 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 | a0001c0001t0002g0265 a0001c0001t0002g0308 a0001c0001t0002g0309 |
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 | 204 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(201): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): 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 | a0001c0001t0001g0127 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.325+11397T>A | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44376961 | |||||||
| chr5:44377150 | G | C | 1 | a0001c0001t0003g0307 | 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 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | 1 | a0001c0001t0001g0016 | 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 | a0001c0001t0009g0253 | 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 | a0001c0001t0003g0291 | 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 | a0001c0001t0002g0056 a0001c0001t0002g0091 a0001c0001t0016g0010 others(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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | 5 | a0001c0001t0008g0002 a0001c0001t0008g0041 a0001c0001t0008g0042 others(2): 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 | 62 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(59): 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 | 65 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(62): 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 | a0001c0001t0010g0218 a0001c0001t0010g0219 a0001c0001t0010g0220 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0004g0232 | 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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0075 a0001c0001t0005g0076 |
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 | a0001c0001t0039g0100 | 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 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
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 | a0001c0001t0002g0092 | 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 | a0001c0001t0013g0118 a0001c0001t0019g0052 |
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 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
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 | a0001c0001t0007g0033 | 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 | 75 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(72): 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0012g0203 a0001c0001t0012g0204 a0001c0001t0012g0205 |
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 | a0001c0001t0002g0054 | 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 | a0001c0001t0039g0100 | 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 | 2 | a0001c0001t0001g0005 a0001c0001t0001g0123 |
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 | 2 | a0001c0001t0001g0022 a0001c0001t0034g0209 |
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 | a0001c0001t0003g0261 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0047g0313 | 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 | 6 | a0001c0001t0001g0022 a0001c0001t0001g0208 a0001c0001t0002g0088 others(3): 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 | 27 | a0001c0001t0001g0122 a0001c0001t0004g0023 a0001c0001t0004g0230 others(24): 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 | a0001c0001t0013g0121 | 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 | 21 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(18): 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 | a0001c0001t0002g0090 | 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 | 75 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(72): 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 | a0003c0003t0032g0045 | 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 | 306 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.325+6399G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44381959 | |||||||
| chr5:44382239 | T | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(18): 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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0002g0091 | 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0010g0218 a0001c0001t0010g0219 a0001c0001t0010g0220 others(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 | 144 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(141): Show |
159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.325+5618G>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44382740 | |||||||
| chr5:44382794 | T | C | 23 | a0001c0001t0004g0023 a0001c0001t0004g0232 a0001c0001t0004g0233 others(20): 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 | a0001c0001t0002g0308 a0001c0001t0002g0309 |
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 | a0001c0001t0002g0216 | 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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | a0001c0001t0001g0103 a0001c0001t0003g0108 a0001c0001t0003g0109 others(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 | a0001c0001t0002g0117 | 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 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0258 others(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 | 51 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(48): 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 | a0001c0001t0007g0039 | 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 | 9 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(6): 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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | 9 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(6): 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 | a0003c0003t0032g0045 | 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 | a0003c0003t0032g0045 | 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 | 201 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(198): Show |
229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): 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 | a0001c0001t0011g0119 a0001c0001t0011g0120 a0001c0001t0011g0310 others(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 | a0001c0001t0018g0228 a0001c0001t0018g0229 |
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 | a0001c0001t0001g0213 | 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 | a0001c0001t0004g0252 | 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 | a0001c0001t0013g0118 a0001c0001t0019g0052 |
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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | 25 | a0001c0001t0004g0023 a0001c0001t0004g0230 a0001c0001t0004g0232 others(22): 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 | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(117): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0002g0054 a0003c0003t0032g0045 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0019g0052 | 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 | a0001c0001t0009g0253 a0001c0001t0009g0254 a0001c0001t0009g0255 |
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 | 303 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(300): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0003c0003t0032g0045 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
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 | 204 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(201): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.325+923T>G | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44387435 | |||||||
| chr5:44387741 | C | CCAAAA | 8 | a0001c0001t0007g0009 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): 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 | 59 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0300 others(56): 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 | a0001c0001t0011g0310 a0001c0001t0011g0311 |
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 | a0001c0001t0045g0312 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.325+152C>T | FGF10 | ENSG00000070193.5 | transcript | ENST00000264664.5 | protein_coding | 1/2 | chr5 | 44388206 |