| geneid | 2263 |
|---|---|
| ensemblid | ENSG00000066468.24 |
| hgncid | 3689 |
| symbol | FGFR2 |
| name | fibroblast growth factor receptor 2 |
| refseq_nuc | NM_000141.5 |
| refseq_prot | NP_000132.3 |
| ensembl_nuc | ENST00000358487.10 |
| ensembl_prot | ENSP00000351276.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 121478332 |
| end | 121598444 |
| strand | - |
| ver | v1.2 |
| region | chr10:121478332-121598444 |
| region5000 | chr10:121473332-121603444 |
| regionname0 | FGFR2_chr10_121478332_121598444 |
| regionname5000 | FGFR2_chr10_121473332_121603444 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 821 | 194 | 58 | 40 | 68 | 6 | 20 | 38 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002 | 0/0 | 821 | 43 | 29 | 6 | 8 | 0 | 0 | 6 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0003 | 0/0 | 821 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0004 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2466 | 140 | 27 | 31 | 63 | 4 | 14 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0002 | 1/0 | 2466 | 42 | 23 | 6 | 5 | 2 | 5 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0003 | 0/0 | 2466 | 39 | 25 | 6 | 8 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0004 | 0/0 | 2466 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0005 | 0/0 | 2466 | 4 | 2 | 1 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0006 | 0/0 | 2466 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0007 | 0/0 | 2466 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0008 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0009 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0010 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0011 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0012 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| c0013 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2159 | 52 | 4 | 18 | 20 | 3 | 7 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0002 | 0/0 | 2159 | 49 | 7 | 7 | 28 | 1 | 6 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0003 | 0/0 | 2159 | 31 | 21 | 3 | 5 | 1 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0004 | 1/0 | 2159 | 28 | 25 | 0 | 0 | 0 | 2 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0005 | 0/0 | 2159 | 13 | 1 | 3 | 8 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0006 | 0/0 | 2159 | 12 | 2 | 0 | 10 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0007 | 0/0 | 2159 | 11 | 3 | 3 | 5 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0008 | 0/0 | 2159 | 7 | 2 | 4 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0009 | 0/0 | 2159 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0010 | 0/0 | 2159 | 5 | 4 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0011 | 0/0 | 2159 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0012 | 0/0 | 2159 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0013 | 0/0 | 2159 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0014 | 0/1 | 2159 | 2 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0015 | 0/0 | 2159 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0016 | 0/0 | 2159 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0017 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0018 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0019 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0020 | 0/0 | 2159 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0021 | 0/0 | 2159 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0022 | 0/0 | 2159 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0023 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0024 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0025 | 0/0 | 2159 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0026 | 0/0 | 2159 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| t0027 | 0/0 | 2159 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2466 | 140 | 27 | 31 | 63 | 4 | 14 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002 | 1/0 | 2466 | 42 | 23 | 6 | 5 | 2 | 5 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0004 | 0/0 | 2466 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0005 | 0/0 | 2466 | 4 | 2 | 1 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0009 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0010 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0012 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0013 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003 | 0/0 | 2466 | 39 | 25 | 6 | 8 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0006 | 0/0 | 2466 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0011 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0003c0007 | 0/0 | 2466 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0004c0008 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4624 | 38 | 3 | 14 | 17 | 1 | 3 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0002 | 0/0 | 4624 | 36 | 1 | 6 | 22 | 1 | 6 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0003 | 0/0 | 4624 | 11 | 4 | 1 | 4 | 1 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0004 | 0/0 | 4624 | 8 | 7 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0005 | 0/0 | 4624 | 6 | 1 | 1 | 4 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0006 | 0/0 | 4624 | 11 | 1 | 0 | 10 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0007 | 0/0 | 4624 | 7 | 1 | 2 | 4 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0008 | 0/0 | 4624 | 4 | 1 | 2 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0009 | 0/0 | 4624 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0011 | 0/0 | 4624 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0012 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0014 | 0/1 | 4624 | 2 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0015 | 0/0 | 4624 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0017 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0018 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0019 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0020 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0021 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0022 | 0/0 | 4624 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0023 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0001t0027 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0001 | 0/0 | 4624 | 12 | 1 | 3 | 2 | 2 | 4 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0002 | 0/0 | 4624 | 7 | 4 | 1 | 2 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0003 | 0/0 | 4624 | 5 | 5 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0004 | 1/0 | 4624 | 7 | 6 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0005 | 0/0 | 4624 | 2 | 0 | 1 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0007 | 0/0 | 4624 | 2 | 1 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0008 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0009 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0012 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0013 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0016 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0002t0025 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0004t0002 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0004t0003 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0004t0004 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0005t0004 | 0/0 | 4624 | 2 | 1 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0005t0007 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0005t0008 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0009t0004 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0010t0008 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0012t0024 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0001c0013t0003 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0001 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0002 | 0/0 | 4624 | 4 | 1 | 0 | 3 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0003 | 0/0 | 4624 | 11 | 9 | 1 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0004 | 0/0 | 4624 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0005 | 0/0 | 4624 | 5 | 0 | 1 | 4 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0007 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0009 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0010 | 0/0 | 4624 | 5 | 4 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0012 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0013 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0016 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0003t0026 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0006t0003 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0006t0004 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0006t0006 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0002c0011t0004 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0003c0007t0001 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0003c0007t0002 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| a0004c0008t0003 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | copy fasta | chr10 | 121473332 | 121603444 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0008g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0011g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0014g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0015g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0015g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0020g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0021g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0022g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0023g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0001t0027g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0016g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0002t0025g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0004t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0004t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0005t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0005t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0005t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0005t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0009t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0010t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0012t0024g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0001c0013t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0010g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0003t0026g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0006t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0006t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0006t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0002c0011t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0003c0007t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0003c0007t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| a0004c0008t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0207 | EUR | GBR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0019 | EUR | GBR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0146 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00621 | hp2 | a0002 | c0003 | t0005 | g0176 | EAS | CHS | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00642 | hp1 | a0001 | c0002 | t0005 | g0167 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0092 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0208 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0206 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01109 | hp1 | a0002 | c0003 | t0007 | g0155 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0165 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01168 | hp2 | a0001 | c0013 | t0003 | g0124 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01175 | hp2 | a0002 | c0003 | t0010 | g0002 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01243 | hp1 | a0002 | c0003 | t0026 | g0238 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01243 | hp2 | a0001 | c0001 | t0014 | g0117 | AMR | PUR | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01257 | hp1 | a0001 | c0010 | t0008 | g0194 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0001 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01258 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01261 | hp1 | a0001 | c0005 | t0008 | g0231 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01346 | hp1 | a0002 | c0003 | t0003 | g0157 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0049 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01884 | hp2 | a0001 | c0002 | t0013 | g0217 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01891 | hp1 | a0002 | c0003 | t0004 | g0220 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01928 | hp2 | a0001 | c0001 | t0021 | g0189 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01978 | hp1 | a0001 | c0002 | t0025 | g0237 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02004 | hp1 | a0002 | c0003 | t0005 | g0184 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0185 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02055 | hp1 | a0002 | c0003 | t0004 | g0214 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CDX | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02165 | hp1 | a0002 | c0003 | t0003 | g0149 | EAS | CDX | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02165 | hp2 | a0001 | c0002 | t0007 | g0164 | EAS | CDX | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0013 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02257 | hp2 | a0002 | c0003 | t0010 | g0005 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0127 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0145 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02280 | hp2 | a0002 | c0003 | t0010 | g0006 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02572 | hp2 | a0001 | c0002 | t0016 | g0200 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02615 | hp1 | a0001 | c0004 | t0002 | g0103 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0137 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0128 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02622 | hp2 | a0004 | c0008 | t0003 | g0120 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0166 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0007 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02698 | hp2 | a0001 | c0005 | t0004 | g0196 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02717 | hp1 | a0001 | c0002 | t0008 | g0224 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02717 | hp2 | a0002 | c0003 | t0003 | g0139 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02723 | hp1 | a0002 | c0011 | t0004 | g0201 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02735 | hp2 | a0001 | c0001 | t0022 | g0234 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02818 | hp2 | a0002 | c0003 | t0013 | g0205 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02895 | hp2 | a0002 | c0003 | t0003 | g0122 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02896 | hp1 | a0002 | c0003 | t0003 | g0161 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02896 | hp2 | a0002 | c0003 | t0010 | g0003 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0162 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02922 | hp2 | a0002 | c0003 | t0004 | g0221 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0233 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02976 | hp2 | a0002 | c0006 | t0003 | g0154 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0209 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03098 | hp1 | a0002 | c0003 | t0016 | g0225 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03098 | hp2 | a0002 | c0003 | t0012 | g0119 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03130 | hp2 | a0002 | c0003 | t0009 | g0009 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0134 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0136 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03225 | hp2 | a0002 | c0003 | t0009 | g0008 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0212 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03453 | hp2 | a0002 | c0003 | t0002 | g0114 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0121 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03486 | hp2 | a0001 | c0004 | t0004 | g0202 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0159 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0160 | SAS | PJL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03516 | hp2 | a0001 | c0002 | t0013 | g0218 | AFR | ESN | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0215 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0158 | AFR | GWD | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0099 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0210 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03942 | hp2 | a0001 | c0002 | t0005 | g0181 | SAS | BEB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | STU | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0223 | SAS | STU | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | STU | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18522 | hp1 | a0001 | c0002 | t0009 | g0014 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0130 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | CHB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0062 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18949 | hp1 | a0002 | c0003 | t0005 | g0190 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18971 | hp2 | a0002 | c0003 | t0005 | g0174 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18977 | hp2 | a0001 | c0001 | t0027 | g0239 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18989 | hp2 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18990 | hp1 | a0003 | c0007 | t0002 | g0023 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19011 | hp1 | a0003 | c0007 | t0001 | g0022 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19030 | hp1 | a0002 | c0003 | t0010 | g0004 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19030 | hp2 | a0002 | c0006 | t0006 | g0193 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19043 | hp1 | a0002 | c0003 | t0004 | g0232 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19043 | hp2 | a0001 | c0005 | t0004 | g0213 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19063 | hp1 | a0001 | c0001 | t0020 | g0179 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19088 | hp1 | a0002 | c0003 | t0005 | g0177 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19240 | hp1 | a0002 | c0003 | t0003 | g0133 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA19240 | hp2 | a0002 | c0006 | t0004 | g0219 | AFR | YRI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20129 | hp1 | a0001 | c0009 | t0004 | g0197 | AFR | ASW | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ASW | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | TSI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | TSI | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0235 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0222 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02559 | hp1 | a0001 | c0012 | t0024 | g0236 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG02559 | hp2 | a0002 | c0003 | t0003 | g0156 | AFR | ACB | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03471 | hp1 | a0002 | c0003 | t0004 | g0203 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0131 | AFR | MSL | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20300 | hp1 | a0001 | c0005 | t0007 | g0140 | AFR | USA | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| NA21309 | hp2 | a0002 | c0003 | t0003 | g0163 | AFR | LWK | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0118 | REF | REF | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0004 | g0227 | REF | REF | FGFR2_chr10_121473332_121603444 | FGFR2 | chr10 | 121473332 | 121603444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:121551357
|
A | G | 1 | a0002 | 43 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
missense_variant | MODERATE | c.557T>C | p.Met186Thr | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/18 | 1190/4624 | 557/2466 | 186/821 | chr10 | 121551357 | ||
| chr10:121593784
|
C | T | 1 | a0004 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.34G>A | p.Val12Met | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/18 | 667/4624 | 34/2466 | 12/821 | chr10 | 121593784 | ||
| chr10:121593801
|
C | G | 1 | a0003 | 2 | NA18990.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.17G>C | p.Arg6Pro | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/18 | 650/4624 | 17/2466 | 6/821 | chr10 | 121593801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:121488036
|
G | A | 3 | a0001c0004a0001c0005a0002c0006 | 11 | HG01261.hp1 HG02258.hp1 HG02615.hp1 others(8): Show |
synonymous_variant | LOW | c.1941C>T | p.Leu647Leu | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/18 | 2574/4624 | 1941/2466 | 647/821 | chr10 | 121488036 | ||
| chr10:121517461
|
G | A | 1 | a0001c0013 | 1 | HG01168.hp2 | splice_region_variant&synonymous_variant | LOW | c.942C>T | p.Ala314Ala | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/18 | 1575/4624 | 942/2466 | 314/821 | chr10 | 121517461 | ||
| chr10:121520162
|
C | T | 1 | a0001c0012 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.756G>A | p.Ser252Ser | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/18 | 1389/4624 | 756/2466 | 252/821 | chr10 | 121520162 | ||
| chr10:121538644
|
T | C | 8 | a0001c0001a0001c0005a0001c0009others(5): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
synonymous_variant | LOW | c.696A>G | p.Val232Val | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/18 | 1329/4624 | 696/2466 | 232/821 | chr10 | 121538644 | ||
| chr10:121565520
|
C | T | 1 | a0001c0010 | 1 | HG01257.hp1 | synonymous_variant | LOW | c.294G>A | p.Thr98Thr | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/18 | 927/4624 | 294/2466 | 98/821 | chr10 | 121565520 | ||
| chr10:121565655
|
C | T | 1 | a0001c0009 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.159G>A | p.Ala53Ala | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/18 | 792/4624 | 159/2466 | 53/821 | chr10 | 121565655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:121478556
|
G | A | 1 | a0001c0001t0014 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1301C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 1301 | chr10 | 121478556 | |||||
| chr10:121478632
|
A | T | 1 | a0001c0001t0020 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1225T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 1225 | chr10 | 121478632 | |||||
| chr10:121479183
|
C | A | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*674G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 674 | chr10 | 121479183 | |||||
| chr10:121479253
|
C | T | 1 | a0001c0001t0019 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 604 | chr10 | 121479253 | |||||
| chr10:121479388
|
C | T | 5 | a0001c0001t0012a0001c0002t0012a0001c0002t0016others(2): Show | 5 | HG02572.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*469G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 469 | chr10 | 121479388 | |||||
| chr10:121479454
|
T | C | 1 | a0001c0001t0011 | 3 | HG01257.hp2 HG01258.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*403A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 403 | chr10 | 121479454 | |||||
| chr10:121479567
|
G | A | 1 | a0001c0001t0018 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 290 | chr10 | 121479567 | |||||
| chr10:121479598
|
G | A | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(19): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*259C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 259 | chr10 | 121479598 | |||||
| chr10:121479673
|
G | A | 2 | a0001c0002t0013a0002c0003t0013 | 3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 18/18 | 184 | chr10 | 121479673 | |||||
| chr10:121593878
|
C | A | 1 | a0001c0001t0021 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/18 | 61 | chr10 | 121593878 | |||||
| chr10:121597968
|
T | C | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0012others(13): Show | 48 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-157A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4151 | chr10 | 121597968 | |||||
| chr10:121598047
|
C | G | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(10): Show | 40 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-236G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4230 | chr10 | 121598047 | |||||
| chr10:121598047
|
C | T | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
5_prime_UTR_variant | MODIFIER | c.-236G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4230 | chr10 | 121598047 | |||||
| chr10:121598129
|
C | G | 4 | a0001c0001t0009a0001c0001t0018a0001c0002t0009others(1): Show | 7 | HG02257.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-318G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4312 | chr10 | 121598129 | |||||
| chr10:121598148
|
T | C | 1 | a0001c0001t0022 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-337A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4331 | chr10 | 121598148 | |||||
| chr10:121598169
|
G | A | 1 | a0001c0001t0023 | 1 | HG02109.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-358C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | chr10 | 121598169 | ||||||
| chr10:121598232
|
G | A | 1 | a0001c0012t0024 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-421C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4415 | chr10 | 121598232 | |||||
| chr10:121598269
|
G | T | 2 | a0001c0001t0017a0002c0003t0010 | 6 | HG01175.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-458C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4452 | chr10 | 121598269 | |||||
| chr10:121598272
|
C | T | 1 | a0001c0002t0025 | 1 | HG01978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-461G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4455 | chr10 | 121598272 | |||||
| chr10:121598298
|
G | A | 1 | a0001c0002t0025 | 1 | HG01978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-487C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4481 | chr10 | 121598298 | |||||
| chr10:121598426
|
G | C | 1 | a0002c0003t0026 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-615C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4609 | chr10 | 121598426 | |||||
| chr10:121598437
|
G | C | 1 | a0001c0001t0027 | 1 | NA18977.hp2 | 5_prime_UTR_variant | MODIFIER | c.-626C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/18 | 4620 | chr10 | 121598437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:121480240
|
G | T | 1 | a0002c0003t0007g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2302-219C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480240 | ||||||
| chr10:121480463
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0101 | 2 | NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2302-442G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480463 | ||||||
| chr10:121480568
|
G | T | 3 | a0001c0001t0006g0173a0002c0003t0002g0062a0002c0003t0002g0073 | 3 | NA18612.hp1 NA18943.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2302-547C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480568 | ||||||
| chr10:121480762
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2302-741C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480762 | ||||||
| chr10:121480762
|
GA | G | 10 | a0001c0001t0018g0013a0001c0002t0002g0099a0001c0002t0003g0138others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2302-742delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480762 | ||||||
| chr10:121480773
|
T | C | 233 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2302-752A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480773 | ||||||
| chr10:121480824
|
C | A | 1 | a0001c0005t0007g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2302-803G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480824 | ||||||
| chr10:121480860
|
G | A | 3 | a0001c0001t0003g0129a0001c0001t0004g0211a0001c0012t0024g0236 | 3 | HG02258.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2302-839C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480860 | ||||||
| chr10:121480867
|
T | C | 1 | a0002c0003t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2302-846A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480867 | ||||||
| chr10:121480938
|
G | T | 1 | a0001c0001t0027g0239 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2302-917C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121480938 | ||||||
| chr10:121481111
|
A | G | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020others(131): Show | 134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.2302-1090T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481111 | ||||||
| chr10:121481131
|
C | T | 50 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2302-1110G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481131 | ||||||
| chr10:121481389
|
GAC | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0003g0135others(10): Show | 13 | HG00609.hp2 HG01168.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2302-1370_2302-136 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481389 | ||||||
| chr10:121481389
|
GACAC | G | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2302-1372_2302-136 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481389 | ||||||
| chr10:121481389
|
GACACAC | G | 3 | a0001c0001t0002g0110a0001c0001t0004g0230a0001c0001t0023g0235 | 3 | HG02109.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2302-1374_2302-136 others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481389 | ||||||
| chr10:121481389
|
GACACACA others(1): Show |
G | 8 | a0001c0001t0002g0034a0001c0001t0002g0101a0001c0004t0002g0103others(5): Show | 8 | HG02280.hp2 HG02615.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2302-1376_2302-136 others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481389 | ||||||
| chr10:121481389
|
GACACACA others(3): Show |
G | 123 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020others(120): Show | 123 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2302-1378_2302-136 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481389 | ||||||
| chr10:121481563
|
C | A | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2302-1542G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481563 | ||||||
| chr10:121481608
|
C | G | 2 | a0001c0001t0002g0071a0001c0002t0002g0078 | 2 | HG01981.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2302-1587G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481608 | ||||||
| chr10:121481609
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2302-1588G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481609 | ||||||
| chr10:121481809
|
G | A | 4 | a0001c0001t0002g0088a0001c0002t0002g0079a0001c0002t0002g0109others(1): Show | 4 | HG01928.hp1 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2302-1788C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481809 | ||||||
| chr10:121481818
|
G | A | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2302-1797C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481818 | ||||||
| chr10:121481827
|
C | CT | 4 | a0001c0001t0002g0034a0001c0001t0006g0170a0002c0003t0010g0003others(1): Show | 4 | HG02896.hp2 NA19074.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2302-1807dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481827 | ||||||
| chr10:121481827
|
C | CTT | 74 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020others(71): Show | 74 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2302-1808_2302-180 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481827 | ||||||
| chr10:121481827
|
C | CTTT | 35 | a0001c0001t0002g0037a0001c0001t0002g0048a0001c0001t0002g0054others(32): Show | 35 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2302-1809_2302-180 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481827 | ||||||
| chr10:121481834
|
A | T | 121 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020others(118): Show | 121 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.2302-1813T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481834 | ||||||
| chr10:121481840
|
A | T | 131 | a0001c0001t0001g0093a0001c0001t0002g0017a0001c0001t0002g0018others(128): Show | 131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.2302-1819T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481840 | ||||||
| chr10:121481841
|
T | A | 9 | a0001c0001t0002g0088a0001c0001t0002g0110a0001c0001t0004g0230others(6): Show | 9 | HG01928.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2302-1820A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481841 | ||||||
| chr10:121481842
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2302-1821A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481842 | ||||||
| chr10:121481846
|
T | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2302-1825A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481846 | ||||||
| chr10:121481847
|
T | A | 5 | a0001c0001t0002g0088a0001c0001t0017g0007a0001c0002t0002g0079others(2): Show | 5 | HG01928.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2302-1826A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481847 | ||||||
| chr10:121481859
|
C | T | 99 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.2302-1838G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481859 | ||||||
| chr10:121481869
|
C | T | 122 | a0001c0001t0001g0046a0001c0001t0002g0017a0001c0001t0002g0018others(119): Show | 122 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2301+1829G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481869 | ||||||
| chr10:121481875
|
C | T | 5 | a0001c0001t0012g0158a0001c0002t0012g0121a0001c0002t0016g0200others(2): Show | 5 | HG02572.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2301+1823G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481875 | ||||||
| chr10:121481982
|
T | C | 233 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2301+1716A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121481982 | ||||||
| chr10:121482013
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2301+1685T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482013 | ||||||
| chr10:121482076
|
A | T | 1 | a0001c0002t0016g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2301+1622T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482076 | ||||||
| chr10:121482102
|
G | A | 11 | a0001c0002t0003g0138a0001c0004t0002g0103a0001c0004t0003g0127others(8): Show | 11 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2301+1596C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482102 | ||||||
| chr10:121482280
|
C | T | 125 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020others(122): Show | 125 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2301+1418G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482280 | ||||||
| chr10:121482281
|
C | T | 2 | a0002c0003t0002g0114a0002c0003t0004g0203 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2301+1417G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482281 | ||||||
| chr10:121482437
|
T | A | 1 | a0002c0003t0010g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2301+1261A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482437 | ||||||
| chr10:121482512
|
T | C | 201 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2301+1186A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482512 | ||||||
| chr10:121482985
|
C | A | 1 | a0001c0001t0002g0058 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2301+713G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482985 | ||||||
| chr10:121482994
|
G | A | 20 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(17): Show | 20 | HG00621.hp2 HG01261.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.2301+704C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121482994 | ||||||
| chr10:121483075
|
G | A | 18 | a0001c0001t0002g0088a0001c0002t0003g0138a0001c0004t0002g0103others(15): Show | 18 | HG01261.hp1 HG01928.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2301+623C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483075 | ||||||
| chr10:121483076
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2301+622G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483076 | ||||||
| chr10:121483105
|
A | G | 2 | a0001c0002t0012g0121a0001c0002t0016g0200 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2301+593T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483105 | ||||||
| chr10:121483164
|
A | C | 1 | a0001c0002t0002g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2301+534T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483164 | ||||||
| chr10:121483207
|
A | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0036 | 2 | HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2301+491T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483207 | ||||||
| chr10:121483210
|
T | C | 198 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2301+488A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483210 | ||||||
| chr10:121483211
|
A | G | 14 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(11): Show | 14 | HG00621.hp2 HG01433.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2301+487T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483211 | ||||||
| chr10:121483266
|
G | C | 212 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2301+432C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483266 | ||||||
| chr10:121483301
|
C | T | 1 | a0001c0001t0005g0183 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2301+397G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483301 | ||||||
| chr10:121483453
|
C | T | 1 | a0001c0002t0009g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2301+245G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483453 | ||||||
| chr10:121483683
|
G | A | 93 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.2301+15C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 17/17 | chr10 | 121483683 | ||||||
| chr10:121484148
|
C | CT | 8 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(5): Show | 8 | HG00621.hp2 HG01433.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2196-346dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484148 | ||||||
| chr10:121484153
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(5): Show | 8 | HG00621.hp2 HG01433.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2196-350G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484153 | ||||||
| chr10:121484216
|
G | A | 210 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2196-413C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484216 | ||||||
| chr10:121484417
|
G | A | 4 | a0001c0004t0003g0127a0001c0004t0004g0215a0002c0006t0003g0154others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2196-614C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484417 | ||||||
| chr10:121484610
|
A | G | 4 | a0001c0004t0003g0127a0001c0004t0004g0215a0002c0006t0003g0154others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2195+785T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484610 | ||||||
| chr10:121484666
|
T | C | 1 | a0001c0002t0004g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2195+729A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484666 | ||||||
| chr10:121484907
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2195+488C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484907 | ||||||
| chr10:121484909
|
T | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2195+486A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484909 | ||||||
| chr10:121484912
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2195+483C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484912 | ||||||
| chr10:121484913
|
G | T | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2195+482C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121484913 | ||||||
| chr10:121485014
|
C | T | 1 | a0002c0003t0010g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2195+381G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121485014 | ||||||
| chr10:121485036
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(2): Show | 5 | HG00621.hp2 HG01433.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2195+359C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121485036 | ||||||
| chr10:121485163
|
C | T | 6 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(3): Show | 6 | HG00621.hp2 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2195+232G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121485163 | ||||||
| chr10:121485320
|
C | T | 16 | a0001c0001t0001g0042a0001c0001t0002g0110a0001c0001t0004g0230others(13): Show | 16 | HG00621.hp2 HG01433.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2195+75G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 16/17 | chr10 | 121485320 | ||||||
| chr10:121485680
|
G | A | 3 | a0001c0001t0003g0129a0001c0001t0004g0211a0001c0012t0024g0236 | 3 | HG02258.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2058-148C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121485680 | ||||||
| chr10:121486474
|
G | A | 1 | a0001c0001t0004g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2057+880C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121486474 | ||||||
| chr10:121486784
|
G | A | 17 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0002g0045others(14): Show | 17 | HG00558.hp1 HG02027.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.2057+570C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121486784 | ||||||
| chr10:121486829
|
G | C | 2 | a0001c0001t0018g0013a0001c0002t0002g0099 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2057+525C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121486829 | ||||||
| chr10:121487060
|
A | G | 1 | a0002c0003t0004g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2057+294T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121487060 | ||||||
| chr10:121487098
|
G | A | 87 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.2057+256C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121487098 | ||||||
| chr10:121487203
|
C | A | 1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2057+151G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121487203 | ||||||
| chr10:121487218
|
TTTCTAAG others(15): Show |
T | 93 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.2057+114_2057+135d others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121487218 | ||||||
| chr10:121487296
|
G | A | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2057+58C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 15/17 | chr10 | 121487296 | ||||||
| chr10:121487523
|
C | T | 85 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.1987-99G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487523 | ||||||
| chr10:121487530
|
T | C | 122 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1987-106A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487530 | ||||||
| chr10:121487553
|
A | G | 2 | a0002c0003t0003g0133a0002c0003t0003g0134 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1987-129T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487553 | ||||||
| chr10:121487589
|
A | C | 3 | a0001c0002t0012g0121a0001c0002t0016g0200a0002c0003t0004g0214 | 3 | HG02055.hp1 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1987-165T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487589 | ||||||
| chr10:121487590
|
T | G | 3 | a0001c0002t0012g0121a0001c0002t0016g0200a0002c0003t0004g0214 | 3 | HG02055.hp1 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1987-166A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487590 | ||||||
| chr10:121487650
|
A | C | 1 | a0001c0001t0019g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1987-226T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487650 | ||||||
| chr10:121487662
|
C | T | 35 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(32): Show | 35 | HG01192.hp2 HG01261.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1987-238G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487662 | ||||||
| chr10:121487716
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1986+275A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487716 | ||||||
| chr10:121487916
|
T | A | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1986+75A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 14/17 | chr10 | 121487916 | ||||||
| chr10:121488130
|
A | C | 2 | a0001c0001t0002g0110a0002c0003t0005g0176 | 2 | HG00621.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1864-17T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488130 | ||||||
| chr10:121488155
|
AC | A | 29 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(26): Show | 29 | HG01192.hp2 HG01261.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1864-43delG | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488155 | ||||||
| chr10:121488159
|
C | T | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1864-46G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488159 | ||||||
| chr10:121488211
|
T | C | 1 | a0002c0003t0004g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1864-98A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488211 | ||||||
| chr10:121488237
|
T | TA | 105 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0046others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1864-125dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488237 | ||||||
| chr10:121488243
|
A | G | 2 | a0002c0003t0002g0114a0002c0003t0004g0203 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1864-130T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488243 | ||||||
| chr10:121488393
|
T | C | 1 | a0001c0001t0006g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1864-280A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488393 | ||||||
| chr10:121488485
|
G | A | 1 | a0001c0001t0002g0060 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1864-372C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488485 | ||||||
| chr10:121488540
|
CA | C | 86 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.1864-428delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488540 | ||||||
| chr10:121488540
|
CAA | C | 18 | a0001c0001t0002g0110a0001c0001t0003g0129a0001c0001t0004g0211others(15): Show | 18 | HG00621.hp2 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1864-429_1864-428d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488540 | ||||||
| chr10:121488540
|
CAAA | C | 124 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0046others(121): Show | 124 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1864-430_1864-428d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488540 | ||||||
| chr10:121488637
|
T | A | 131 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1864-524A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488637 | ||||||
| chr10:121488693
|
C | T | 4 | a0001c0001t0005g0187a0001c0001t0017g0007a0001c0002t0003g0138others(1): Show | 4 | HG02647.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1864-580G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121488693 | ||||||
| chr10:121489076
|
G | GT | 31 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(28): Show | 31 | HG01192.hp2 HG01261.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1864-964dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489076 | ||||||
| chr10:121489093
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1864-980T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489093 | ||||||
| chr10:121489136
|
G | A | 1 | a0001c0001t0027g0239 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1864-1023C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489136 | ||||||
| chr10:121489149
|
C | T | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1864-1036G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489149 | ||||||
| chr10:121489210
|
C | T | 235 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1864-1097G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489210 | ||||||
| chr10:121489272
|
C | T | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1864-1159G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489272 | ||||||
| chr10:121489318
|
T | C | 236 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1864-1205A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489318 | ||||||
| chr10:121489394
|
G | T | 6 | a0001c0001t0003g0129a0001c0001t0004g0211a0001c0002t0002g0079others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864-1281C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489394 | ||||||
| chr10:121489543
|
T | C | 6 | a0001c0001t0002g0088a0001c0001t0007g0123a0001c0001t0019g0136others(3): Show | 6 | HG01192.hp2 HG01884.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864-1430A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489543 | ||||||
| chr10:121489712
|
C | T | 1 | a0002c0003t0010g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1864-1599G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489712 | ||||||
| chr10:121489725
|
A | T | 5 | a0001c0001t0004g0230a0001c0001t0005g0187a0001c0001t0017g0007others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864-1612T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121489725 | ||||||
| chr10:121490154
|
CT | C | 168 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1864-2042delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490154
|
CTT | C | 5 | a0001c0001t0001g0083a0001c0001t0002g0094a0001c0001t0002g0110others(2): Show | 5 | HG01496.hp1 HG02698.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1864-2043_1864-204 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490154
|
CTTT | C | 8 | a0001c0001t0002g0088a0001c0001t0007g0123a0001c0001t0019g0136others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1864-2044_1864-204 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490154
|
CTTTT | C | 10 | a0001c0001t0001g0051a0001c0004t0003g0127a0001c0004t0004g0215others(7): Show | 10 | HG01261.hp1 HG01346.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1864-2045_1864-204 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490154
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1864-2055_1864-204 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490154
|
CTTTTTTT others(8): Show |
C | 9 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0008g0208others(6): Show | 9 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1864-2056_1864-204 others(19): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490154 | ||||||
| chr10:121490216
|
T | G | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1864-2103A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490216 | ||||||
| chr10:121490367
|
T | C | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1864-2254A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490367 | ||||||
| chr10:121490378
|
G | A | 27 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(24): Show | 27 | HG01192.hp2 HG01261.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1864-2265C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490378 | ||||||
| chr10:121490415
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1864-2302G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490415 | ||||||
| chr10:121490424
|
A | G | 5 | a0001c0001t0004g0199a0001c0002t0002g0113a0001c0002t0003g0137others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1864-2311T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490424 | ||||||
| chr10:121490460
|
G | A | 1 | a0001c0004t0004g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1864-2347C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490460 | ||||||
| chr10:121490492
|
G | A | 2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864-2379C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490492 | ||||||
| chr10:121490733
|
C | T | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1864-2620G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490733 | ||||||
| chr10:121490734
|
G | A | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1864-2621C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490734 | ||||||
| chr10:121490764
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0014g0117a0001c0001t0014g0118others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864-2651G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490764 | ||||||
| chr10:121490870
|
G | A | 2 | a0001c0001t0002g0110a0002c0003t0005g0176 | 2 | HG00621.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1864-2757C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490870 | ||||||
| chr10:121490946
|
G | C | 1 | a0001c0013t0003g0124 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1864-2833C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121490946 | ||||||
| chr10:121491060
|
G | A | 2 | a0001c0001t0002g0110a0002c0003t0005g0176 | 2 | HG00621.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1864-2947C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491060 | ||||||
| chr10:121491149
|
A | G | 2 | a0001c0001t0002g0029a0001c0002t0002g0072 | 2 | NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1864-3036T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491149 | ||||||
| chr10:121491298
|
A | AAGTAATC others(41): Show |
2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1864-3186_1864-318 others(52): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491298 | ||||||
| chr10:121491342
|
C | G | 234 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1864-3229G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491342 | ||||||
| chr10:121491346
|
C | T | 234 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1864-3233G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491346 | ||||||
| chr10:121491592
|
T | C | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1864-3479A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491592 | ||||||
| chr10:121491594
|
A | G | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1864-3481T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491594 | ||||||
| chr10:121491598
|
T | C | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1864-3485A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491598 | ||||||
| chr10:121491695
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1864-3582G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491695 | ||||||
| chr10:121491802
|
A | G | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1864-3689T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491802 | ||||||
| chr10:121491819
|
G | A | 4 | a0001c0002t0002g0099a0001c0002t0012g0121a0001c0002t0016g0200others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1864-3706C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491819 | ||||||
| chr10:121491873
|
C | CA | 66 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0027others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.1864-3761dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491873 | ||||||
| chr10:121491873
|
C | CAA | 40 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0039others(37): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1864-3762_1864-376 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121491873 | ||||||
| chr10:121492187
|
G | A | 11 | a0001c0004t0002g0103a0001c0004t0003g0127a0001c0004t0004g0202others(8): Show | 11 | HG01261.hp1 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1864-4074C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492187 | ||||||
| chr10:121492221
|
G | T | 4 | a0001c0001t0003g0150a0002c0003t0002g0062a0002c0003t0002g0073others(1): Show | 4 | HG02165.hp1 NA18943.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1864-4108C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492221 | ||||||
| chr10:121492375
|
A | G | 236 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1863+4157T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492375 | ||||||
| chr10:121492421
|
CAT | C | 13 | a0001c0001t0003g0129a0001c0001t0004g0211a0001c0002t0002g0079others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1863+4109_1863+411 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492421 | ||||||
| chr10:121492451
|
G | A | 1 | a0001c0002t0008g0224 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1863+4081C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492451 | ||||||
| chr10:121492896
|
C | G | 12 | a0001c0001t0001g0053a0001c0004t0002g0103a0001c0004t0003g0127others(9): Show | 12 | HG01261.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1863+3636G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492896 | ||||||
| chr10:121492963
|
A | G | 1 | a0001c0013t0003g0124 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1863+3569T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121492963 | ||||||
| chr10:121493018
|
A | G | 225 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1863+3514T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493018 | ||||||
| chr10:121493063
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0005g0181 | 3 | HG03491.hp1 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1863+3469G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493063 | ||||||
| chr10:121493482
|
T | C | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1863+3050A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493482 | ||||||
| chr10:121493530
|
G | C | 2 | a0001c0005t0004g0213a0002c0006t0006g0193 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1863+3002C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493530 | ||||||
| chr10:121493537
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1863+2995C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493537 | ||||||
| chr10:121493567
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1863+2965G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493567 | ||||||
| chr10:121493574
|
C | T | 3 | a0001c0001t0002g0088a0001c0002t0013g0217a0001c0002t0013g0218 | 3 | HG01884.hp2 HG01928.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1863+2958G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493574 | ||||||
| chr10:121493646
|
A | G | 11 | a0001c0001t0005g0187a0001c0001t0006g0186a0001c0002t0002g0099others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1863+2886T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493646 | ||||||
| chr10:121493687
|
G | A | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1863+2845C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493687 | ||||||
| chr10:121493705
|
C | T | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1863+2827G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493705 | ||||||
| chr10:121493783
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1863+2749G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493783 | ||||||
| chr10:121493819
|
T | A | 1 | a0001c0002t0007g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1863+2713A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493819 | ||||||
| chr10:121493869
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1863+2663G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493869 | ||||||
| chr10:121493931
|
G | C | 2 | a0001c0002t0001g0082a0001c0002t0007g0164 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1863+2601C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493931 | ||||||
| chr10:121493949
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1863+2583A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493949 | ||||||
| chr10:121493953
|
A | G | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1863+2579T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121493953 | ||||||
| chr10:121494509
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1863+2023C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121494509 | ||||||
| chr10:121494850
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1863+1682C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121494850 | ||||||
| chr10:121494952
|
G | A | 5 | a0001c0001t0004g0211a0001c0012t0024g0236a0002c0003t0001g0092others(2): Show | 5 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1863+1580C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121494952 | ||||||
| chr10:121495251
|
G | A | 4 | a0001c0001t0002g0034a0001c0001t0002g0101a0002c0003t0004g0214others(1): Show | 4 | HG02055.hp1 HG03098.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1863+1281C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121495251 | ||||||
| chr10:121495394
|
G | A | 2 | a0001c0004t0003g0127a0002c0006t0003g0154 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1863+1138C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121495394 | ||||||
| chr10:121495624
|
A | G | 1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1863+908T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121495624 | ||||||
| chr10:121496171
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1863+361A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121496171 | ||||||
| chr10:121496222
|
A | T | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1863+310T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121496222 | ||||||
| chr10:121496286
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1863+246A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121496286 | ||||||
| chr10:121496333
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1863+199C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 13/17 | chr10 | 121496333 | ||||||
| chr10:121496815
|
C | CT | 5 | a0001c0001t0001g0042a0001c0001t0002g0101a0001c0001t0006g0173others(2): Show | 5 | HG01433.hp2 NA18612.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.1673-94dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496815 | ||||||
| chr10:121496815
|
CT | C | 5 | a0001c0001t0003g0135a0001c0001t0007g0143a0001c0001t0009g0010others(2): Show | 5 | HG01884.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1673-94delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496815 | ||||||
| chr10:121496817
|
T | A | 1 | a0002c0003t0002g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1673-95A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496817 | ||||||
| chr10:121496856
|
C | G | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1673-134G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496856 | ||||||
| chr10:121496893
|
G | A | 5 | a0001c0001t0004g0211a0001c0012t0024g0236a0002c0003t0001g0092others(2): Show | 5 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673-171C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496893 | ||||||
| chr10:121496951
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1673-229G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496951 | ||||||
| chr10:121496995
|
G | A | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1673-273C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121496995 | ||||||
| chr10:121497032
|
G | A | 4 | a0001c0001t0003g0129a0001c0002t0002g0079a0001c0002t0002g0109others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1673-310C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497032 | ||||||
| chr10:121497118
|
G | A | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1673-396C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497118 | ||||||
| chr10:121497130
|
C | CA | 14 | a0001c0001t0001g0053a0001c0001t0003g0150a0001c0001t0005g0187others(11): Show | 14 | HG02486.hp1 HG02572.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.1673-409dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497130 | ||||||
| chr10:121497130
|
CA | C | 164 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1673-409delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497130 | ||||||
| chr10:121497147
|
A | G | 2 | a0001c0004t0003g0127a0002c0006t0003g0154 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1673-425T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497147 | ||||||
| chr10:121497190
|
C | T | 1 | a0001c0001t0004g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1673-468G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497190 | ||||||
| chr10:121497374
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0002g0101 | 2 | NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1673-652T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497374 | ||||||
| chr10:121497489
|
A | C | 9 | a0001c0001t0003g0135a0001c0001t0006g0186a0001c0001t0009g0010others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1673-767T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497489 | ||||||
| chr10:121497831
|
G | A | 2 | a0001c0001t0005g0187a0001c0002t0008g0224 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1672+664C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497831 | ||||||
| chr10:121497888
|
A | C | 221 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1672+607T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497888 | ||||||
| chr10:121497930
|
C | T | 2 | a0002c0003t0004g0214a0002c0003t0012g0119 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1672+565G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121497930 | ||||||
| chr10:121498104
|
G | A | 1 | a0001c0002t0003g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1672+391C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121498104 | ||||||
| chr10:121498341
|
T | C | 1 | a0001c0001t0019g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1672+154A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121498341 | ||||||
| chr10:121498459
|
A | G | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1672+36T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 12/17 | chr10 | 121498459 | ||||||
| chr10:121498720
|
A | C | 1 | a0001c0001t0004g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1562-115T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121498720 | ||||||
| chr10:121498795
|
T | G | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1562-190A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121498795 | ||||||
| chr10:121498840
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0003g0153 | 2 | HG02129.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1562-235C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121498840 | ||||||
| chr10:121498907
|
A | G | 1 | a0001c0001t0002g0020 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1562-302T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121498907 | ||||||
| chr10:121499238
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1562-633C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499238 | ||||||
| chr10:121499504
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1562-899C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499504 | ||||||
| chr10:121499785
|
C | A | 2 | a0001c0001t0015g0159a0001c0001t0015g0160 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1561+1041G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499785 | ||||||
| chr10:121499825
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1561+1001A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499825 | ||||||
| chr10:121499879
|
A | C | 1 | a0002c0003t0010g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1561+947T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499879 | ||||||
| chr10:121499989
|
C | A | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1561+837G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121499989 | ||||||
| chr10:121500102
|
G | A | 2 | a0002c0003t0004g0214a0002c0003t0012g0119 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1561+724C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500102 | ||||||
| chr10:121500299
|
C | T | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1561+527G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500299 | ||||||
| chr10:121500392
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1561+434A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500392 | ||||||
| chr10:121500441
|
T | G | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1561+385A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500441 | ||||||
| chr10:121500493
|
C | T | 5 | a0001c0001t0017g0007a0001c0004t0003g0127a0001c0004t0004g0215others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561+333G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500493 | ||||||
| chr10:121500610
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1561+216C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500610 | ||||||
| chr10:121500678
|
C | T | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1561+148G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500678 | ||||||
| chr10:121500731
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1561+95G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500731 | ||||||
| chr10:121500754
|
T | C | 2 | a0001c0001t0005g0187a0001c0002t0008g0224 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1561+72A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 11/17 | chr10 | 121500754 | ||||||
| chr10:121501054
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1440-107C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501054 | ||||||
| chr10:121501167
|
T | A | 1 | a0001c0001t0007g0143 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1440-220A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501167 | ||||||
| chr10:121501178
|
G | A | 8 | a0001c0001t0002g0088a0001c0001t0004g0211a0001c0012t0024g0236others(5): Show | 8 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1440-231C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501178 | ||||||
| chr10:121501195
|
G | A | 4 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440-248C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501195 | ||||||
| chr10:121501551
|
C | T | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1440-604G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501551 | ||||||
| chr10:121501591
|
C | T | 2 | a0001c0002t0003g0138a0001c0002t0008g0224 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1440-644G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501591 | ||||||
| chr10:121501795
|
T | A | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1440-848A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501795 | ||||||
| chr10:121501979
|
T | C | 2 | a0001c0001t0002g0088a0001c0002t0002g0072 | 2 | HG01928.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1440-1032A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121501979 | ||||||
| chr10:121502005
|
C | T | 8 | a0001c0001t0002g0088a0001c0001t0004g0211a0001c0012t0024g0236others(5): Show | 8 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1440-1058G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502005 | ||||||
| chr10:121502013
|
A | G | 2 | a0002c0003t0004g0214a0002c0003t0012g0119 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1440-1066T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502013 | ||||||
| chr10:121502048
|
A | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0115 | 2 | NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1440-1101T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502048 | ||||||
| chr10:121502066
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1440-1119C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502066 | ||||||
| chr10:121502180
|
C | T | 188 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1440-1233G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502180 | ||||||
| chr10:121502363
|
T | G | 4 | a0001c0001t0001g0053a0001c0002t0013g0217a0001c0002t0013g0218others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440-1416A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502363 | ||||||
| chr10:121502376
|
G | C | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1439+1414C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502376 | ||||||
| chr10:121502417
|
T | C | 1 | a0002c0003t0005g0176 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1439+1373A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502417 | ||||||
| chr10:121502448
|
A | G | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1439+1342T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502448 | ||||||
| chr10:121502533
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1439+1257C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502533 | ||||||
| chr10:121502547
|
G | A | 6 | a0001c0001t0002g0037a0001c0001t0002g0064a0001c0001t0007g0165others(3): Show | 6 | HG00140.hp1 HG01168.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1439+1243C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502547 | ||||||
| chr10:121502636
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1439+1154A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502636 | ||||||
| chr10:121502642
|
G | T | 8 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1439+1148C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502642 | ||||||
| chr10:121502794
|
G | C | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1439+996C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502794 | ||||||
| chr10:121502854
|
T | G | 196 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1439+936A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502854 | ||||||
| chr10:121502936
|
C | T | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1439+854G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502936 | ||||||
| chr10:121502978
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0012g0158a0001c0002t0001g0090others(3): Show | 6 | HG00735.hp1 HG02622.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1439+812G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121502978 | ||||||
| chr10:121503018
|
C | A | 2 | a0001c0001t0005g0182a0001c0001t0021g0189 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1439+772G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503018 | ||||||
| chr10:121503151
|
A | G | 1 | a0001c0001t0007g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1439+639T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503151 | ||||||
| chr10:121503165
|
C | T | 3 | a0001c0002t0008g0224a0002c0003t0004g0214a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1439+625G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503165 | ||||||
| chr10:121503181
|
G | C | 7 | a0001c0001t0002g0088a0001c0001t0004g0211a0001c0012t0024g0236others(4): Show | 7 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1439+609C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503181 | ||||||
| chr10:121503194
|
G | A | 187 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1439+596C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503194 | ||||||
| chr10:121503412
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1439+378G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503412 | ||||||
| chr10:121503423
|
A | G | 3 | a0002c0003t0004g0233a0002c0003t0009g0009a0002c0003t0010g0002 | 3 | HG01175.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1439+367T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503423 | ||||||
| chr10:121503436
|
G | T | 1 | a0002c0003t0003g0157 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1439+354C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503436 | ||||||
| chr10:121503455
|
A | G | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1439+335T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503455 | ||||||
| chr10:121503509
|
G | A | 2 | a0001c0002t0002g0079a0001c0002t0002g0109 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1439+281C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503509 | ||||||
| chr10:121503616
|
A | T | 2 | a0001c0001t0004g0198a0001c0001t0009g0012 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1439+174T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503616 | ||||||
| chr10:121503625
|
T | C | 2 | a0001c0001t0004g0230a0001c0001t0019g0136 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1439+165A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 10/17 | chr10 | 121503625 | ||||||
| chr10:121503956
|
C | T | 1 | a0001c0002t0003g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1288-15G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121503956 | ||||||
| chr10:121503964
|
C | G | 7 | a0001c0001t0002g0088a0001c0001t0004g0211a0001c0012t0024g0236others(4): Show | 7 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1288-23G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121503964 | ||||||
| chr10:121503976
|
T | C | 2 | a0001c0002t0013g0217a0001c0002t0013g0218 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1288-35A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121503976 | ||||||
| chr10:121504102
|
C | T | 45 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1288-161G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504102 | ||||||
| chr10:121504187
|
T | C | 1 | a0001c0001t0006g0171 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1288-246A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504187 | ||||||
| chr10:121504258
|
C | T | 1 | a0001c0001t0003g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1288-317G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504258 | ||||||
| chr10:121504277
|
C | T | 1 | a0002c0003t0010g0003 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1288-336G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504277 | ||||||
| chr10:121504295
|
C | CCTGGAG | 8 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0009g0012others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288-355_1288-354i others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504295 | ||||||
| chr10:121504296
|
A | C | 8 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0009g0012others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288-355T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504296 | ||||||
| chr10:121504336
|
C | T | 187 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1288-395G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504336 | ||||||
| chr10:121504341
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1288-400C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504341 | ||||||
| chr10:121504393
|
T | C | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1288-452A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504393 | ||||||
| chr10:121504456
|
C | G | 1 | a0002c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1288-515G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504456 | ||||||
| chr10:121504572
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1288-631A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504572 | ||||||
| chr10:121504830
|
GA | G | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1288-890delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504830 | ||||||
| chr10:121504847
|
A | G | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1288-906T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504847 | ||||||
| chr10:121504905
|
G | C | 2 | a0001c0001t0007g0123a0001c0013t0003g0124 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1288-964C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504905 | ||||||
| chr10:121504934
|
C | T | 6 | a0001c0002t0013g0217a0001c0002t0013g0218a0001c0004t0002g0103others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288-993G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504934 | ||||||
| chr10:121504954
|
A | T | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1288-1013T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504954 | ||||||
| chr10:121504978
|
C | A | 8 | a0001c0001t0001g0053a0001c0002t0013g0217a0001c0002t0013g0218others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288-1037G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504978 | ||||||
| chr10:121504999
|
G | A | 1 | a0001c0001t0018g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1288-1058C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121504999 | ||||||
| chr10:121505199
|
G | C | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1288-1258C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505199 | ||||||
| chr10:121505417
|
C | A | 1 | a0001c0001t0002g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1288-1476G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505417 | ||||||
| chr10:121505475
|
T | G | 1 | a0001c0001t0004g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1288-1534A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505475 | ||||||
| chr10:121505539
|
A | G | 1 | a0001c0001t0022g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1288-1598T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505539 | ||||||
| chr10:121505746
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1288-1805A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505746 | ||||||
| chr10:121505792
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1288-1851A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121505792 | ||||||
| chr10:121506319
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1288-2378G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506319 | ||||||
| chr10:121506357
|
C | CA | 24 | a0001c0001t0001g0025a0001c0001t0001g0056a0001c0001t0004g0198others(21): Show | 24 | HG00140.hp2 HG01243.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1288-2417dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506357 | ||||||
| chr10:121506357
|
C | CAA | 182 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1288-2418_1288-241 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506357 | ||||||
| chr10:121506357
|
C | CAAA | 6 | a0001c0001t0002g0026a0001c0001t0002g0100a0001c0001t0023g0235others(3): Show | 6 | HG00738.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1288-2419_1288-241 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506357 | ||||||
| chr10:121506357
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0019g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1288-2431_1288-241 others(19): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506357 | ||||||
| chr10:121506377
|
G | A | 1 | a0001c0001t0008g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1288-2436C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506377 | ||||||
| chr10:121506410
|
C | T | 2 | a0001c0001t0001g0053a0001c0005t0004g0196 | 2 | HG02486.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1288-2469G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506410 | ||||||
| chr10:121506461
|
G | A | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1288-2520C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506461 | ||||||
| chr10:121506715
|
G | C | 9 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(6): Show | 9 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288-2774C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506715 | ||||||
| chr10:121506718
|
C | T | 1 | a0002c0003t0013g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1288-2777G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506718 | ||||||
| chr10:121506726
|
C | A | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1288-2785G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506726 | ||||||
| chr10:121506947
|
C | T | 20 | a0001c0001t0003g0151a0001c0001t0004g0204a0001c0001t0004g0216others(17): Show | 20 | HG01109.hp1 HG01175.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1288-3006G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121506947 | ||||||
| chr10:121507025
|
C | T | 2 | a0001c0001t0015g0159a0001c0001t0015g0160 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1288-3084G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507025 | ||||||
| chr10:121507038
|
T | C | 9 | a0001c0001t0002g0088a0001c0001t0003g0129a0001c0001t0004g0211others(6): Show | 9 | HG00621.hp2 HG00738.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288-3097A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507038 | ||||||
| chr10:121507205
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1288-3264C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507205 | ||||||
| chr10:121507237
|
G | A | 2 | a0002c0003t0004g0214a0002c0003t0012g0119 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1288-3296C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507237 | ||||||
| chr10:121507246
|
T | C | 6 | a0001c0001t0018g0013a0001c0002t0003g0138a0001c0002t0008g0224others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1288-3305A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507246 | ||||||
| chr10:121507492
|
G | A | 186 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1288-3551C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507492 | ||||||
| chr10:121507893
|
C | A | 1 | a0001c0002t0008g0224 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1288-3952G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507893 | ||||||
| chr10:121507894
|
C | A | 1 | a0001c0001t0004g0223 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1288-3953G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507894 | ||||||
| chr10:121507921
|
C | A | 4 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-3980G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121507921 | ||||||
| chr10:121508117
|
G | T | 118 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(115): Show | 118 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1288-4176C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121508117 | ||||||
| chr10:121508209
|
C | T | 3 | a0001c0001t0019g0136a0001c0004t0004g0215a0002c0003t0016g0225 | 3 | HG03098.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1288-4268G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121508209 | ||||||
| chr10:121508255
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1288-4314A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121508255 | ||||||
| chr10:121508614
|
C | T | 8 | a0001c0001t0001g0098a0001c0001t0002g0037a0001c0001t0002g0064others(5): Show | 8 | HG00140.hp1 HG00544.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288-4673G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121508614 | ||||||
| chr10:121508959
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1288-5018C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121508959 | ||||||
| chr10:121509023
|
G | A | 2 | a0001c0001t0019g0136a0002c0003t0016g0225 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1288-5082C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509023 | ||||||
| chr10:121509029
|
C | T | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1288-5088G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509029 | ||||||
| chr10:121509165
|
C | A | 2 | a0001c0001t0014g0117a0001c0001t0014g0118 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1288-5224G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509165 | ||||||
| chr10:121509375
|
T | G | 60 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0066others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1288-5434A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509375 | ||||||
| chr10:121509385
|
T | A | 4 | a0001c0001t0001g0053a0001c0001t0023g0235a0001c0005t0004g0196others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-5444A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509385 | ||||||
| chr10:121509421
|
G | GT | 30 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0083others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1288-5481dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509421 | ||||||
| chr10:121509421
|
GT | G | 10 | a0001c0001t0006g0170a0001c0001t0008g0206a0001c0001t0008g0207others(7): Show | 11 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1288-5481delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509421 | ||||||
| chr10:121509421
|
GTT | G | 63 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0066others(60): Show | 63 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1288-5482_1288-548 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509421 | ||||||
| chr10:121509482
|
C | CTT | 6 | a0001c0002t0002g0109a0001c0002t0005g0181a0001c0002t0012g0121others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288-5543_1288-554 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509482 | ||||||
| chr10:121509482
|
CT | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1288-5542delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509482 | ||||||
| chr10:121509482
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0011t0004g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1288-5556_1288-554 others(19): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509482 | ||||||
| chr10:121509495
|
T | G | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1288-5554A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509495 | ||||||
| chr10:121509502
|
TTTTTTTT others(1): Show |
T | 57 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0066others(54): Show | 57 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1288-5569_1288-556 others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509502 | ||||||
| chr10:121509509
|
TG | T | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1288-5569delC | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509509 | ||||||
| chr10:121509627
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1287+5490C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509627 | ||||||
| chr10:121509676
|
T | G | 1 | a0001c0002t0002g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1287+5441A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509676 | ||||||
| chr10:121509685
|
G | A | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287+5432C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509685 | ||||||
| chr10:121509793
|
A | C | 8 | a0001c0001t0004g0230a0001c0001t0018g0013a0001c0002t0013g0217others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1287+5324T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509793 | ||||||
| chr10:121509802
|
T | G | 2 | a0002c0006t0003g0154a0002c0006t0004g0219 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1287+5315A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509802 | ||||||
| chr10:121509865
|
T | C | 1 | a0002c0003t0005g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1287+5252A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509865 | ||||||
| chr10:121509986
|
C | G | 1 | a0002c0003t0002g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1287+5131G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121509986 | ||||||
| chr10:121510197
|
T | C | 133 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1287+4920A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510197 | ||||||
| chr10:121510365
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1287+4752C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510365 | ||||||
| chr10:121510389
|
G | A | 1 | a0001c0001t0005g0175 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1287+4728C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510389 | ||||||
| chr10:121510399
|
A | G | 235 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1287+4718T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510399 | ||||||
| chr10:121510412
|
A | G | 1 | a0001c0004t0003g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1287+4705T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510412 | ||||||
| chr10:121510603
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287+4514A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510603 | ||||||
| chr10:121510666
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1287+4451C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510666 | ||||||
| chr10:121510702
|
C | T | 2 | a0001c0001t0007g0123a0001c0013t0003g0124 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1287+4415G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510702 | ||||||
| chr10:121510778
|
A | ATTTAT | 22 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0002g0028others(19): Show | 22 | HG00140.hp2 HG00558.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1287+4334_1287+433 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
A | ATTTATTT others(3): Show |
58 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0066others(55): Show | 58 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1287+4329_1287+433 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
A | ATTTATTT others(8): Show |
9 | a0001c0001t0001g0053a0001c0001t0003g0135a0001c0002t0004g0209others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+4324_1287+433 others(19): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
A | ATTTATTT others(13): Show |
1 | a0002c0003t0004g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+4319_1287+433 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
A | ATTTATTT others(18): Show |
1 | a0002c0003t0012g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1287+4314_1287+433 others(29): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
A | ATTTATTT others(23): Show |
2 | a0001c0001t0019g0136a0002c0003t0016g0225 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1287+4309_1287+433 others(34): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510778
|
ATTTAT | A | 6 | a0001c0001t0004g0230a0001c0001t0018g0013a0001c0002t0013g0217others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287+4334_1287+433 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510778 | ||||||
| chr10:121510824
|
C | G | 65 | a0001c0001t0001g0031a0001c0001t0001g0053a0001c0001t0001g0055others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1287+4293G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121510824 | ||||||
| chr10:121511216
|
C | T | 2 | a0001c0001t0006g0171a0001c0001t0006g0188 | 2 | HG02083.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1287+3901G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511216 | ||||||
| chr10:121511530
|
A | T | 2 | a0001c0001t0019g0136a0002c0003t0016g0225 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1287+3587T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511530 | ||||||
| chr10:121511545
|
T | G | 156 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1287+3572A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511545 | ||||||
| chr10:121511618
|
G | A | 22 | a0001c0001t0002g0048a0001c0001t0003g0129a0001c0001t0003g0135others(19): Show | 22 | HG00621.hp2 HG00738.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1287+3499C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511618 | ||||||
| chr10:121511625
|
A | G | 172 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1287+3492T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511625 | ||||||
| chr10:121511632
|
G | A | 23 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0002g0034others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1287+3485C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511632 | ||||||
| chr10:121511873
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1287+3244T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511873 | ||||||
| chr10:121511888
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1287+3229C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511888 | ||||||
| chr10:121511957
|
G | A | 21 | a0001c0001t0003g0129a0001c0001t0003g0135a0001c0001t0004g0211others(18): Show | 21 | HG00621.hp2 HG00738.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287+3160C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121511957 | ||||||
| chr10:121512019
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1287+3098G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512019 | ||||||
| chr10:121512025
|
G | A | 5 | a0001c0002t0001g0019a0001c0002t0001g0024a0001c0002t0001g0038others(2): Show | 5 | HG00099.hp2 HG00642.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287+3092C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512025 | ||||||
| chr10:121512180
|
A | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1287+2937T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512180 | ||||||
| chr10:121512324
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1287+2793G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512324 | ||||||
| chr10:121512366
|
T | C | 3 | a0001c0002t0002g0113a0001c0002t0003g0137a0002c0006t0004g0219 | 3 | HG02615.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1287+2751A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512366 | ||||||
| chr10:121512495
|
C | T | 215 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1287+2622G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512495 | ||||||
| chr10:121512598
|
T | C | 1 | a0001c0001t0006g0170 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1287+2519A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512598 | ||||||
| chr10:121512751
|
G | A | 2 | a0001c0001t0004g0230a0001c0001t0018g0013 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1287+2366C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512751 | ||||||
| chr10:121512782
|
G | A | 112 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(109): Show | 113 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1287+2335C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512782 | ||||||
| chr10:121512809
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1287+2308G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512809 | ||||||
| chr10:121512902
|
T | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+2215A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512902 | ||||||
| chr10:121512903
|
C | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+2214G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512903 | ||||||
| chr10:121512921
|
G | A | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1287+2196C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512921 | ||||||
| chr10:121512922
|
C | T | 1 | a0002c0003t0002g0073 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1287+2195G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512922 | ||||||
| chr10:121512923
|
G | A | 18 | a0001c0001t0001g0052a0001c0002t0001g0019a0001c0002t0001g0024others(15): Show | 18 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1287+2194C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121512923 | ||||||
| chr10:121513106
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+2011A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513106 | ||||||
| chr10:121513153
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0002g0112a0001c0001t0006g0173others(2): Show | 5 | HG02155.hp1 NA18612.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+1964G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513153 | ||||||
| chr10:121513308
|
C | T | 1 | a0002c0003t0003g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1287+1809G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513308 | ||||||
| chr10:121513402
|
T | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+1715A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513402 | ||||||
| chr10:121513439
|
C | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+1678G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513439 | ||||||
| chr10:121513444
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+1673T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513444 | ||||||
| chr10:121513461
|
A | C | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1287+1656T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513461 | ||||||
| chr10:121513565
|
A | G | 205 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1287+1552T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513565 | ||||||
| chr10:121513919
|
G | A | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1287+1198C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513919 | ||||||
| chr10:121513936
|
T | C | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1287+1181A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121513936 | ||||||
| chr10:121514176
|
G | C | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1287+941C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121514176 | ||||||
| chr10:121514512
|
C | A | 2 | a0001c0001t0005g0187a0001c0001t0006g0186 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1287+605G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121514512 | ||||||
| chr10:121514548
|
C | A | 5 | a0001c0001t0001g0055a0001c0002t0001g0033a0001c0002t0001g0063others(2): Show | 5 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+569G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121514548 | ||||||
| chr10:121514613
|
A | C | 205 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1287+504T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121514613 | ||||||
| chr10:121514904
|
C | T | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1287+213G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 9/17 | chr10 | 121514904 | ||||||
| chr10:121515332
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1085-13A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121515332 | ||||||
| chr10:121515531
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1085-212A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121515531 | ||||||
| chr10:121515541
|
C | T | 4 | a0001c0002t0002g0113a0001c0002t0003g0137a0001c0002t0003g0138others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-222G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121515541 | ||||||
| chr10:121515575
|
G | T | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1085-256C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121515575 | ||||||
| chr10:121515619
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1085-300G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121515619 | ||||||
| chr10:121516148
|
T | C | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1085-829A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516148 | ||||||
| chr10:121516152
|
C | T | 41 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0002t0001g0019others(38): Show | 41 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1085-833G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516152 | ||||||
| chr10:121516304
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1085-985A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516304 | ||||||
| chr10:121516364
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1084+955A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516364 | ||||||
| chr10:121516410
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1084+909A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516410 | ||||||
| chr10:121516577
|
G | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0030others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1084+742C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516577 | ||||||
| chr10:121516599
|
A | G | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1084+720T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516599 | ||||||
| chr10:121516776
|
G | A | 41 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0002t0001g0019others(38): Show | 41 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1084+543C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516776 | ||||||
| chr10:121516786
|
C | T | 204 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1084+533G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516786 | ||||||
| chr10:121516792
|
G | A | 1 | a0001c0002t0002g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1084+527C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121516792 | ||||||
| chr10:121517047
|
A | G | 1 | a0002c0003t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1084+272T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121517047 | ||||||
| chr10:121517198
|
C | G | 1 | a0001c0002t0001g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1084+121G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121517198 | ||||||
| chr10:121517215
|
T | C | 2 | a0002c0003t0005g0174a0003c0007t0001g0022 | 2 | NA18971.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1084+104A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121517215 | ||||||
| chr10:121517287
|
A | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1084+32T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 8/17 | chr10 | 121517287 | ||||||
| chr10:121517520
|
G | A | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.940-57C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121517520 | ||||||
| chr10:121517541
|
G | A | 1 | a0002c0003t0004g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.940-78C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121517541 | ||||||
| chr10:121517638
|
C | T | 1 | a0002c0003t0007g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.940-175G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121517638 | ||||||
| chr10:121517941
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.940-478A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121517941 | ||||||
| chr10:121517993
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.940-530C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121517993 | ||||||
| chr10:121518087
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0005g0169 | 2 | NA18981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.940-624T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518087 | ||||||
| chr10:121518152
|
G | GTA | 46 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0002t0001g0019others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.940-691_940-690dup others(2): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518152 | ||||||
| chr10:121518228
|
C | T | 204 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.940-765G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518228 | ||||||
| chr10:121518301
|
A | G | 2 | a0001c0001t0004g0198a0001c0001t0007g0166 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.940-838T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518301 | ||||||
| chr10:121518349
|
T | G | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.940-886A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518349 | ||||||
| chr10:121518355
|
C | T | 5 | a0001c0001t0008g0206a0001c0001t0008g0207a0001c0001t0008g0208others(2): Show | 6 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-892G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518355 | ||||||
| chr10:121518997
|
G | A | 1 | a0002c0003t0010g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+982C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121518997 | ||||||
| chr10:121519056
|
G | C | 5 | a0001c0002t0002g0113a0001c0002t0003g0137a0001c0002t0003g0138others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+923C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519056 | ||||||
| chr10:121519186
|
T | G | 4 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0212others(1): Show | 4 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+793A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519186 | ||||||
| chr10:121519227
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.939+752G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519227 | ||||||
| chr10:121519400
|
G | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0027others(63): Show | 67 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.939+579C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519400 | ||||||
| chr10:121519665
|
C | T | 204 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.939+314G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519665 | ||||||
| chr10:121519968
|
A | G | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.939+11T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 7/17 | chr10 | 121519968 | ||||||
| chr10:121520196
|
A | G | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.749-27T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520196 | ||||||
| chr10:121520231
|
C | T | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-62G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520231 | ||||||
| chr10:121520281
|
C | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0002t0001g0019others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.749-112G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520281 | ||||||
| chr10:121520316
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.749-147G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520316 | ||||||
| chr10:121520352
|
C | T | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-183G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520352 | ||||||
| chr10:121520756
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.749-587G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520756 | ||||||
| chr10:121520851
|
T | C | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-682A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520851 | ||||||
| chr10:121520872
|
T | C | 204 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.749-703A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520872 | ||||||
| chr10:121520873
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.749-704C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520873 | ||||||
| chr10:121520880
|
C | T | 2 | a0001c0001t0014g0117a0001c0001t0014g0118 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.749-711G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121520880 | ||||||
| chr10:121521132
|
T | C | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.749-963A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521132 | ||||||
| chr10:121521321
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.749-1152C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521321 | ||||||
| chr10:121521401
|
T | C | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-1232A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521401 | ||||||
| chr10:121521572
|
GCAAATCA others(19): Show |
G | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-1429_749-1404d others(28): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521572 | ||||||
| chr10:121521618
|
G | A | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.749-1449C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521618 | ||||||
| chr10:121521645
|
GA | G | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-1477delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521645 | ||||||
| chr10:121521649
|
A | G | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-1480T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521649 | ||||||
| chr10:121521703
|
G | A | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-1534C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521703 | ||||||
| chr10:121521739
|
A | G | 49 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0027others(46): Show | 49 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.749-1570T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521739 | ||||||
| chr10:121521977
|
A | C | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.749-1808T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121521977 | ||||||
| chr10:121522051
|
C | A | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.749-1882G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522051 | ||||||
| chr10:121522086
|
G | A | 7 | a0002c0003t0003g0122a0002c0003t0003g0156a0002c0003t0003g0157others(4): Show | 7 | HG01109.hp1 HG01346.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.749-1917C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522086 | ||||||
| chr10:121522256
|
A | T | 1 | a0001c0001t0003g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.749-2087T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522256 | ||||||
| chr10:121522314
|
T | C | 1 | a0001c0002t0002g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.749-2145A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522314 | ||||||
| chr10:121522356
|
G | A | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.749-2187C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522356 | ||||||
| chr10:121522507
|
G | A | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.749-2338C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522507 | ||||||
| chr10:121522620
|
T | C | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.749-2451A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522620 | ||||||
| chr10:121522750
|
A | T | 216 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.749-2581T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522750 | ||||||
| chr10:121522926
|
A | C | 216 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.749-2757T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121522926 | ||||||
| chr10:121523047
|
C | T | 205 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.749-2878G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523047 | ||||||
| chr10:121523177
|
G | T | 3 | a0001c0001t0005g0187a0001c0001t0006g0186a0002c0003t0009g0008 | 3 | HG02723.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.749-3008C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523177 | ||||||
| chr10:121523351
|
G | A | 2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.749-3182C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523351 | ||||||
| chr10:121523425
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.749-3256G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523425 | ||||||
| chr10:121523732
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.749-3563C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523732 | ||||||
| chr10:121523757
|
G | A | 1 | a0001c0001t0005g0175 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.749-3588C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523757 | ||||||
| chr10:121523796
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.749-3627A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523796 | ||||||
| chr10:121523894
|
T | C | 1 | a0001c0010t0008g0194 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.749-3725A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121523894 | ||||||
| chr10:121524096
|
A | ATG | 7 | a0001c0001t0002g0060a0001c0001t0003g0129a0001c0001t0004g0204others(4): Show | 7 | HG02165.hp1 HG02965.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.749-3929_749-3928d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524096 | ||||||
| chr10:121524098
|
GTA | G | 59 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0031others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.749-3931_749-3930d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524098 | ||||||
| chr10:121524099
|
T | TACAC | 4 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0009g0010others(1): Show | 4 | HG01433.hp2 HG02004.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-3931_749-3930i others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
T | TGTAC | 3 | a0001c0001t0005g0180a0002c0003t0001g0092a0002c0003t0002g0070 | 3 | HG00738.hp1 NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.749-3931_749-3930i others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATAC | T | 19 | a0001c0001t0002g0020a0001c0001t0002g0112a0001c0001t0004g0223others(16): Show | 20 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.749-3934_749-3931d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATACACA others(1): Show |
T | 6 | a0001c0001t0002g0017a0001c0001t0002g0036a0001c0001t0004g0211others(3): Show | 6 | HG01192.hp1 HG01258.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.749-3938_749-3931d others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATACACA others(3): Show |
T | 1 | a0001c0002t0003g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.749-3940_749-3931d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATACACA others(5): Show |
T | 3 | a0001c0002t0004g0210a0001c0002t0013g0217a0001c0002t0013g0218 | 3 | HG01884.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.749-3942_749-3931d others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATACACA others(7): Show |
T | 25 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0002t0001g0019others(22): Show | 25 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.749-3944_749-3931d others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524099
|
TATACACA others(9): Show |
T | 1 | a0001c0002t0001g0024 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.749-3946_749-3931d others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524099 | ||||||
| chr10:121524100
|
A | G | 4 | a0001c0005t0004g0213a0002c0003t0005g0176a0002c0003t0005g0184others(1): Show | 4 | HG00621.hp2 HG02004.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-3931T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524100 | ||||||
| chr10:121524101
|
T | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.749-3932A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524101 | ||||||
| chr10:121524101
|
T | TAC | 3 | a0002c0003t0010g0005a0002c0003t0010g0006a0002c0006t0003g0154 | 3 | HG02257.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.749-3934_749-3933d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524101 | ||||||
| chr10:121524101
|
T | TACACACA others(3): Show |
2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.749-3942_749-3933d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524101 | ||||||
| chr10:121524101
|
TAC | T | 16 | a0001c0001t0023g0235a0001c0005t0004g0213a0002c0003t0003g0122others(13): Show | 16 | HG01109.hp1 HG01175.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.749-3934_749-3933d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524101 | ||||||
| chr10:121524109
|
C | T | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.749-3940G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524109 | ||||||
| chr10:121524141
|
CA | C | 4 | a0001c0001t0001g0089a0001c0001t0002g0032a0001c0001t0003g0125others(1): Show | 4 | HG00735.hp2 HG02083.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-3973delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524141 | ||||||
| chr10:121524142
|
A | C | 2 | a0001c0001t0001g0057a0001c0001t0003g0151 | 2 | HG02809.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.749-3973T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524142 | ||||||
| chr10:121524144
|
A | ACC | 3 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0116 | 3 | HG00597.hp2 NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.749-3976_749-3975i others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524144 | ||||||
| chr10:121524144
|
A | C | 47 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0041others(44): Show | 47 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.749-3975T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524144 | ||||||
| chr10:121524146
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0002g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.749-3978_749-3977i others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524146 | ||||||
| chr10:121524146
|
A | ACACACCC others(3): Show |
1 | a0001c0001t0014g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.749-3978_749-3977i others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524146 | ||||||
| chr10:121524146
|
A | ACACC | 3 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0002g0102 | 3 | HG00609.hp1 HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.749-3978_749-3977i others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524146 | ||||||
| chr10:121524146
|
A | ACC | 7 | a0001c0001t0001g0050a0001c0001t0002g0034a0001c0001t0002g0101others(4): Show | 7 | HG01099.hp1 HG01099.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.749-3979_749-3978d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524146 | ||||||
| chr10:121524146
|
A | C | 118 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0030others(115): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.749-3977T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524146 | ||||||
| chr10:121524190
|
C | A | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.749-4021G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524190 | ||||||
| chr10:121524307
|
T | C | 1 | a0001c0002t0016g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.749-4138A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524307 | ||||||
| chr10:121524424
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.749-4255T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524424 | ||||||
| chr10:121524526
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.749-4357G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524526 | ||||||
| chr10:121524566
|
G | A | 1 | a0001c0002t0008g0224 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.749-4397C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524566 | ||||||
| chr10:121524581
|
T | G | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.749-4412A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524581 | ||||||
| chr10:121524612
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG01496.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.749-4443T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524612 | ||||||
| chr10:121524718
|
C | T | 1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.749-4549G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524718 | ||||||
| chr10:121524874
|
A | G | 1 | a0002c0003t0003g0157 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.749-4705T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524874 | ||||||
| chr10:121524930
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.749-4761C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524930 | ||||||
| chr10:121524997
|
C | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG01496.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.749-4828G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121524997 | ||||||
| chr10:121525010
|
G | T | 2 | a0001c0001t0006g0172a0001c0001t0007g0146 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.749-4841C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525010 | ||||||
| chr10:121525035
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.749-4866A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525035 | ||||||
| chr10:121525126
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.749-4957C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525126 | ||||||
| chr10:121525624
|
G | GGAGAGAG others(3): Show |
2 | a0002c0003t0004g0214a0002c0003t0012g0119 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.749-5465_749-5456d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525624 | ||||||
| chr10:121525624
|
G | GGAGAGAG others(7): Show |
1 | a0002c0003t0010g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.749-5469_749-5456d others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525624 | ||||||
| chr10:121525624
|
GGA | G | 8 | a0001c0001t0019g0136a0001c0002t0002g0113a0001c0002t0003g0137others(5): Show | 8 | HG02615.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-5457_749-5456d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525624 | ||||||
| chr10:121525624
|
GGAGA | G | 201 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.749-5459_749-5456d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525624 | ||||||
| chr10:121525624
|
GGAGAGAG others(3): Show |
G | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.749-5465_749-5456d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525624 | ||||||
| chr10:121525630
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0002g0102others(1): Show | 4 | HG00609.hp1 HG00621.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-5461T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525630 | ||||||
| chr10:121525728
|
A | C | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.749-5559T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525728 | ||||||
| chr10:121525921
|
A | G | 219 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.749-5752T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121525921 | ||||||
| chr10:121526011
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.749-5842G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526011 | ||||||
| chr10:121526106
|
G | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0036 | 2 | HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.749-5937C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526106 | ||||||
| chr10:121526236
|
A | G | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-6067T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526236 | ||||||
| chr10:121526419
|
C | T | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.749-6250G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526419 | ||||||
| chr10:121526421
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.749-6252G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526421 | ||||||
| chr10:121526699
|
TG | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0005g0183 | 3 | NA18951.hp2 NA19079.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.749-6531delC | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526699 | ||||||
| chr10:121526861
|
T | C | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.749-6692A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121526861 | ||||||
| chr10:121527590
|
CA | C | 194 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.749-7422delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121527590 | ||||||
| chr10:121527592
|
A | T | 8 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(5): Show | 8 | HG01261.hp1 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-7423T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121527592 | ||||||
| chr10:121527691
|
G | T | 194 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.749-7522C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121527691 | ||||||
| chr10:121527835
|
CGAG | C | 6 | a0001c0001t0019g0136a0002c0003t0002g0114a0002c0003t0003g0161others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.749-7669_749-7667d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121527835 | ||||||
| chr10:121527902
|
G | A | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.749-7733C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121527902 | ||||||
| chr10:121528189
|
T | C | 216 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.749-8020A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528189 | ||||||
| chr10:121528213
|
T | C | 205 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.749-8044A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528213 | ||||||
| chr10:121528214
|
G | T | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.749-8045C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528214 | ||||||
| chr10:121528272
|
C | A | 205 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.749-8103G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528272 | ||||||
| chr10:121528484
|
C | T | 15 | a0001c0002t0002g0079a0001c0002t0002g0099a0001c0002t0002g0109others(12): Show | 15 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.749-8315G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528484 | ||||||
| chr10:121528533
|
A | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.749-8364T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528533 | ||||||
| chr10:121528759
|
A | G | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.749-8590T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528759 | ||||||
| chr10:121528868
|
G | GAACA | 3 | a0001c0001t0003g0135a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.749-8703_749-8700d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528868 | ||||||
| chr10:121528875
|
C | T | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.749-8706G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528875 | ||||||
| chr10:121528962
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.749-8793A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121528962 | ||||||
| chr10:121529078
|
C | G | 8 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(5): Show | 8 | HG01261.hp1 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-8909G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529078 | ||||||
| chr10:121529084
|
G | A | 5 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-8915C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529084 | ||||||
| chr10:121529203
|
C | T | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.749-9034G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529203 | ||||||
| chr10:121529220
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.749-9051A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529220 | ||||||
| chr10:121529224
|
T | C | 1 | a0001c0001t0003g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.749-9055A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529224 | ||||||
| chr10:121529259
|
A | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.749-9090T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529259 | ||||||
| chr10:121529350
|
T | C | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.749-9181A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529350 | ||||||
| chr10:121529368
|
T | C | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-9199A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529368 | ||||||
| chr10:121529463
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0002g0086 | 2 | HG01175.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.748+9129A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529463 | ||||||
| chr10:121529486
|
A | G | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.748+9106T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529486 | ||||||
| chr10:121529631
|
T | C | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.748+8961A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121529631 | ||||||
| chr10:121530046
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.748+8546C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530046 | ||||||
| chr10:121530345
|
A | G | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.748+8247T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530345 | ||||||
| chr10:121530377
|
C | T | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.748+8215G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530377 | ||||||
| chr10:121530391
|
C | G | 2 | a0001c0001t0004g0211a0002c0006t0004g0219 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.748+8201G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530391 | ||||||
| chr10:121530554
|
G | A | 29 | a0001c0001t0001g0052a0001c0002t0001g0019a0001c0002t0001g0024others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.748+8038C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530554 | ||||||
| chr10:121530632
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.748+7960G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121530632 | ||||||
| chr10:121531202
|
A | C | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.748+7390T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531202 | ||||||
| chr10:121531220
|
C | T | 16 | a0002c0003t0003g0122a0002c0003t0003g0133a0002c0003t0003g0134others(13): Show | 16 | HG01109.hp1 HG01175.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.748+7372G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531220 | ||||||
| chr10:121531609
|
C | T | 10 | a0001c0002t0002g0079a0001c0002t0002g0099a0001c0002t0002g0109others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+6983G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531609 | ||||||
| chr10:121531625
|
C | T | 5 | a0002c0003t0001g0092a0002c0003t0005g0176a0002c0003t0005g0177others(2): Show | 5 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+6967G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531625 | ||||||
| chr10:121531750
|
G | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(23): Show | 26 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.748+6842C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531750 | ||||||
| chr10:121531982
|
C | G | 1 | a0004c0008t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.748+6610G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121531982 | ||||||
| chr10:121532044
|
C | T | 2 | a0001c0002t0008g0224a0001c0004t0003g0127 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.748+6548G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121532044 | ||||||
| chr10:121532718
|
A | G | 1 | a0001c0001t0020g0179 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.748+5874T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121532718 | ||||||
| chr10:121532770
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.748+5822C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121532770 | ||||||
| chr10:121532935
|
T | C | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+5657A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121532935 | ||||||
| chr10:121533110
|
C | T | 5 | a0002c0003t0004g0214a0002c0003t0010g0003a0002c0003t0010g0004others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.748+5482G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533110 | ||||||
| chr10:121533163
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0002g0048others(3): Show | 6 | HG00438.hp2 HG00597.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+5429G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533163 | ||||||
| chr10:121533198
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748+5394C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533198 | ||||||
| chr10:121533274
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.748+5318G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533274 | ||||||
| chr10:121533316
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.748+5276C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533316 | ||||||
| chr10:121533401
|
G | A | 1 | a0001c0001t0019g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.748+5191C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533401 | ||||||
| chr10:121533464
|
A | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748+5128T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533464 | ||||||
| chr10:121533708
|
G | C | 1 | a0001c0001t0005g0183 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.748+4884C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533708 | ||||||
| chr10:121533750
|
G | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748+4842C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533750 | ||||||
| chr10:121533889
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748+4703A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533889 | ||||||
| chr10:121533912
|
T | G | 2 | a0002c0003t0003g0139a0002c0006t0006g0193 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.748+4680A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121533912 | ||||||
| chr10:121534038
|
C | T | 1 | a0001c0002t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.748+4554G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534038 | ||||||
| chr10:121534067
|
C | T | 1 | a0001c0002t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.748+4525G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534067 | ||||||
| chr10:121534091
|
C | CT | 43 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0046others(40): Show | 43 | HG00438.hp1 HG00735.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.748+4500dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534091
|
C | CTT | 11 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0004g0211others(8): Show | 11 | HG01192.hp2 HG01952.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.748+4499_748+4500d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534091
|
C | CTTT | 19 | a0002c0003t0003g0122a0002c0003t0003g0133a0002c0003t0003g0134others(16): Show | 19 | HG01243.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.748+4498_748+4500d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534091
|
C | CTTTT | 5 | a0002c0003t0007g0155a0002c0003t0009g0009a0002c0003t0010g0002others(2): Show | 5 | HG01109.hp1 HG01175.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.748+4497_748+4500d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534091
|
CT | C | 10 | a0001c0001t0001g0115a0001c0001t0002g0110a0001c0001t0003g0147others(7): Show | 10 | HG00438.hp2 HG02055.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.748+4500delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534091
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0007g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.748+4489_748+4500d others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534091 | ||||||
| chr10:121534121
|
C | T | 3 | a0001c0002t0001g0082a0002c0003t0003g0139a0002c0006t0006g0193 | 3 | HG02523.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.748+4471G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534121 | ||||||
| chr10:121534201
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0074a0001c0001t0001g0091others(4): Show | 7 | HG02717.hp2 NA18612.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.748+4391G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534201 | ||||||
| chr10:121534256
|
C | G | 34 | a0001c0001t0004g0211a0001c0001t0019g0136a0001c0001t0023g0235others(31): Show | 34 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.748+4336G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534256 | ||||||
| chr10:121534259
|
T | C | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.748+4333A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534259 | ||||||
| chr10:121534417
|
T | A | 138 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.748+4175A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534417 | ||||||
| chr10:121534556
|
C | T | 5 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+4036G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534556 | ||||||
| chr10:121534563
|
T | C | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+4029A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534563 | ||||||
| chr10:121534595
|
C | T | 1 | a0001c0001t0008g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.748+3997G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534595 | ||||||
| chr10:121534602
|
A | G | 37 | a0001c0001t0004g0211a0001c0001t0012g0158a0001c0001t0017g0007others(34): Show | 37 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.748+3990T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534602 | ||||||
| chr10:121534632
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.748+3960C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534632 | ||||||
| chr10:121534859
|
A | T | 15 | a0001c0002t0002g0079a0001c0002t0002g0099a0001c0002t0002g0109others(12): Show | 15 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.748+3733T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534859 | ||||||
| chr10:121534941
|
A | C | 2 | a0002c0003t0002g0114a0002c0003t0004g0203 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.748+3651T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121534941 | ||||||
| chr10:121535124
|
A | G | 2 | a0002c0003t0003g0139a0002c0006t0006g0193 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.748+3468T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535124 | ||||||
| chr10:121535178
|
C | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0055others(14): Show | 17 | HG00558.hp2 HG01168.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.748+3414G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535178 | ||||||
| chr10:121535257
|
A | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0002g0075others(5): Show | 8 | HG00544.hp2 HG00597.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.748+3335T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535257 | ||||||
| chr10:121535292
|
G | A | 2 | a0001c0001t0007g0123a0001c0013t0003g0124 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.748+3300C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535292 | ||||||
| chr10:121535364
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.748+3228G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535364 | ||||||
| chr10:121535508
|
A | G | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748+3084T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121535508 | ||||||
| chr10:121536084
|
G | T | 30 | a0001c0001t0023g0235a0002c0003t0002g0114a0002c0003t0003g0122others(27): Show | 30 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.748+2508C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121536084 | ||||||
| chr10:121536305
|
C | A | 1 | a0001c0001t0006g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.748+2287G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121536305 | ||||||
| chr10:121536311
|
C | A | 1 | a0001c0001t0006g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.748+2281G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121536311 | ||||||
| chr10:121536644
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0095others(5): Show | 9 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.748+1948C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121536644 | ||||||
| chr10:121536805
|
G | T | 187 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.748+1787C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121536805 | ||||||
| chr10:121537146
|
A | G | 1 | a0001c0001t0006g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.748+1446T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537146 | ||||||
| chr10:121537226
|
T | G | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.748+1366A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537226 | ||||||
| chr10:121537273
|
T | C | 10 | a0001c0005t0004g0213a0002c0003t0001g0092a0002c0003t0002g0062others(7): Show | 10 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.748+1319A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537273 | ||||||
| chr10:121537338
|
C | T | 5 | a0001c0001t0003g0135a0001c0001t0004g0230a0001c0001t0009g0010others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+1254G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537338 | ||||||
| chr10:121537557
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.748+1035G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537557 | ||||||
| chr10:121537646
|
C | T | 2 | a0002c0003t0003g0139a0002c0006t0006g0193 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.748+946G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537646 | ||||||
| chr10:121537654
|
C | T | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.748+938G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537654 | ||||||
| chr10:121537714
|
C | A | 4 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+878G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537714 | ||||||
| chr10:121537726
|
A | AAG | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.748+865_748+866ins others(2): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121537726 | ||||||
| chr10:121538071
|
C | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0063a0001c0002t0001g0065others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+521G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121538071 | ||||||
| chr10:121538213
|
G | T | 24 | a0001c0001t0023g0235a0002c0003t0002g0114a0002c0003t0003g0122others(21): Show | 24 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.748+379C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 6/17 | chr10 | 121538213 | ||||||
| chr10:121538976
|
T | C | 1 | a0002c0003t0005g0177 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.625-261A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121538976 | ||||||
| chr10:121538989
|
G | A | 1 | a0001c0001t0007g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.625-274C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121538989 | ||||||
| chr10:121539013
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.625-298C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539013 | ||||||
| chr10:121539055
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.625-340G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539055 | ||||||
| chr10:121539056
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-341C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539056 | ||||||
| chr10:121539070
|
C | T | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-355G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539070 | ||||||
| chr10:121539189
|
C | G | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-474G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539189 | ||||||
| chr10:121539242
|
T | G | 2 | a0002c0003t0003g0139a0002c0006t0006g0193 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.625-527A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539242 | ||||||
| chr10:121539760
|
G | C | 1 | a0001c0001t0008g0195 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.625-1045C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539760 | ||||||
| chr10:121539783
|
G | A | 138 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.625-1068C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539783 | ||||||
| chr10:121539923
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.625-1208A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121539923 | ||||||
| chr10:121540246
|
T | A | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-1531A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540246 | ||||||
| chr10:121540254
|
G | T | 1 | a0001c0001t0003g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.625-1539C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540254 | ||||||
| chr10:121540357
|
G | A | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.625-1642C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540357 | ||||||
| chr10:121540402
|
T | C | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.625-1687A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540402 | ||||||
| chr10:121540403
|
T | A | 1 | a0001c0005t0007g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.625-1688A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540403 | ||||||
| chr10:121540411
|
A | T | 5 | a0002c0003t0004g0214a0002c0003t0010g0003a0002c0003t0010g0004others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-1696T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540411 | ||||||
| chr10:121540435
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0004g0204 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-1720C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540435 | ||||||
| chr10:121540525
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-1810C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540525 | ||||||
| chr10:121540528
|
A | G | 2 | a0002c0003t0003g0139a0002c0006t0006g0193 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.625-1813T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540528 | ||||||
| chr10:121540556
|
A | G | 5 | a0002c0003t0004g0214a0002c0003t0010g0003a0002c0003t0010g0004others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-1841T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540556 | ||||||
| chr10:121540752
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.625-2037T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540752 | ||||||
| chr10:121540780
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.625-2065T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540780 | ||||||
| chr10:121540846
|
T | C | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-2131A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121540846 | ||||||
| chr10:121541097
|
G | A | 2 | a0001c0001t0003g0132a0004c0008t0003g0120 | 2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.625-2382C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541097 | ||||||
| chr10:121541171
|
G | T | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-2456C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541171 | ||||||
| chr10:121541456
|
G | T | 2 | a0001c0001t0009g0012a0001c0005t0004g0213 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.625-2741C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541456 | ||||||
| chr10:121541538
|
C | T | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.625-2823G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541538 | ||||||
| chr10:121541608
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.625-2893C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541608 | ||||||
| chr10:121541630
|
G | T | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-2915C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541630 | ||||||
| chr10:121541684
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0004g0204 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-2969C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541684 | ||||||
| chr10:121541786
|
AAATAAAA others(6): Show |
A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-3084_625-3072d others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121541786 | ||||||
| chr10:121542069
|
G | A | 1 | a0002c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-3354C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542069 | ||||||
| chr10:121542099
|
T | C | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-3384A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542099 | ||||||
| chr10:121542258
|
G | C | 1 | a0001c0002t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.625-3543C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542258 | ||||||
| chr10:121542503
|
C | T | 1 | a0001c0001t0006g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.625-3788G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542503 | ||||||
| chr10:121542521
|
C | T | 1 | a0001c0002t0001g0090 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.625-3806G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542521 | ||||||
| chr10:121542885
|
C | T | 1 | a0001c0002t0003g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.625-4170G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542885 | ||||||
| chr10:121542886
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-4171C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542886 | ||||||
| chr10:121542966
|
G | C | 1 | a0002c0003t0013g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.625-4251C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121542966 | ||||||
| chr10:121543260
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.625-4545T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543260 | ||||||
| chr10:121543307
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-4592G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543307 | ||||||
| chr10:121543407
|
G | A | 1 | a0002c0006t0004g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.625-4692C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543407 | ||||||
| chr10:121543442
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.625-4727T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543442 | ||||||
| chr10:121543443
|
G | C | 1 | a0002c0003t0004g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.625-4728C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543443 | ||||||
| chr10:121543582
|
C | G | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-4867G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543582 | ||||||
| chr10:121543636
|
T | G | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-4921A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543636 | ||||||
| chr10:121543764
|
G | A | 30 | a0001c0001t0023g0235a0002c0003t0002g0114a0002c0003t0003g0122others(27): Show | 30 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.625-5049C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543764 | ||||||
| chr10:121543886
|
T | C | 1 | a0001c0002t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.625-5171A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543886 | ||||||
| chr10:121543964
|
A | G | 1 | a0001c0001t0003g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.625-5249T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121543964 | ||||||
| chr10:121544036
|
C | A | 5 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0210others(2): Show | 5 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-5321G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544036 | ||||||
| chr10:121544056
|
G | C | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-5341C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544056 | ||||||
| chr10:121544091
|
T | C | 11 | a0001c0002t0002g0079a0001c0002t0002g0099a0001c0002t0002g0109others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-5376A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544091 | ||||||
| chr10:121544212
|
C | A | 9 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(6): Show | 9 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-5497G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544212 | ||||||
| chr10:121544225
|
A | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG01496.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.625-5510T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544225 | ||||||
| chr10:121544226
|
T | C | 1 | a0001c0002t0003g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.625-5511A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544226 | ||||||
| chr10:121544354
|
A | G | 209 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(206): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.625-5639T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544354 | ||||||
| chr10:121544443
|
T | TA | 13 | a0001c0001t0001g0021a0001c0001t0001g0051a0001c0001t0001g0104others(10): Show | 13 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-5729dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544443 | ||||||
| chr10:121544443
|
TA | T | 26 | a0001c0001t0004g0204a0001c0001t0022g0234a0001c0002t0001g0063others(23): Show | 26 | HG01109.hp1 HG01168.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.625-5729delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544443 | ||||||
| chr10:121544878
|
C | T | 1 | a0001c0005t0007g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.625-6163G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544878 | ||||||
| chr10:121544911
|
G | A | 1 | a0001c0001t0006g0192 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.625-6196C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544911 | ||||||
| chr10:121544972
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-6257C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121544972 | ||||||
| chr10:121545119
|
C | T | 5 | a0002c0003t0004g0214a0002c0003t0010g0003a0002c0003t0010g0004others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+6171G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121545119 | ||||||
| chr10:121545347
|
G | A | 2 | a0001c0002t0008g0224a0001c0004t0003g0127 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.624+5943C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121545347 | ||||||
| chr10:121545392
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624+5898C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121545392 | ||||||
| chr10:121545955
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.624+5335G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121545955 | ||||||
| chr10:121545973
|
T | C | 1 | a0002c0003t0003g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.624+5317A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121545973 | ||||||
| chr10:121546058
|
C | T | 2 | a0002c0003t0003g0133a0002c0003t0003g0134 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.624+5232G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546058 | ||||||
| chr10:121546185
|
T | TA | 135 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.624+5104dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546185
|
T | TAAAAAAA others(1): Show |
17 | a0001c0001t0003g0129a0001c0001t0004g0204a0002c0003t0001g0092others(14): Show | 17 | HG00621.hp2 HG00738.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.624+5097_624+5104d others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546185
|
T | TAAAAAAA others(2): Show |
16 | a0001c0001t0009g0011a0002c0003t0002g0114a0002c0003t0003g0131others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.624+5096_624+5104d others(11): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546185
|
T | TAAAAAAA others(3): Show |
7 | a0001c0001t0009g0010a0002c0003t0007g0155a0002c0003t0010g0002others(4): Show | 7 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+5095_624+5104d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546185
|
T | TAAAAAAA others(4): Show |
5 | a0001c0001t0003g0135a0001c0001t0004g0211a0002c0003t0004g0214others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+5094_624+5104d others(13): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546185
|
T | TAAAAAAA others(5): Show |
5 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0004t0004g0215others(2): Show | 5 | HG01261.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+5093_624+5104d others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546185 | ||||||
| chr10:121546239
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.624+5051G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546239 | ||||||
| chr10:121546254
|
A | G | 15 | a0001c0001t0003g0129a0001c0001t0004g0204a0002c0003t0001g0092others(12): Show | 15 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.624+5036T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546254 | ||||||
| chr10:121546399
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0002g0020a0001c0001t0002g0058 | 3 | HG01099.hp2 NA18954.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.624+4891C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546399 | ||||||
| chr10:121546430
|
T | C | 1 | a0001c0001t0008g0195 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.624+4860A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546430 | ||||||
| chr10:121546482
|
G | A | 1 | a0002c0003t0003g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.624+4808C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546482 | ||||||
| chr10:121546981
|
C | T | 3 | a0001c0001t0007g0143a0001c0004t0002g0103a0001c0004t0004g0202 | 3 | HG02615.hp1 HG03486.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.624+4309G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546981 | ||||||
| chr10:121546982
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.624+4308C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121546982 | ||||||
| chr10:121547092
|
C | T | 3 | a0001c0001t0004g0211a0001c0001t0004g0230a0001c0001t0018g0013 | 3 | HG02257.hp1 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.624+4198G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547092 | ||||||
| chr10:121547168
|
G | A | 40 | a0001c0001t0003g0129a0001c0001t0004g0204a0002c0003t0001g0092others(37): Show | 40 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.624+4122C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547168 | ||||||
| chr10:121547208
|
G | A | 18 | a0002c0003t0003g0122a0002c0003t0003g0131a0002c0003t0003g0133others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.624+4082C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547208 | ||||||
| chr10:121547309
|
A | AATGG | 2 | a0002c0003t0002g0114a0002c0003t0004g0203 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.624+3980_624+3981i others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547309 | ||||||
| chr10:121547400
|
C | CT | 40 | a0001c0001t0003g0129a0001c0001t0004g0204a0002c0003t0001g0092others(37): Show | 40 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.624+3889dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547400 | ||||||
| chr10:121547404
|
T | G | 2 | a0001c0001t0003g0152a0001c0001t0005g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.624+3886A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547404 | ||||||
| chr10:121547522
|
G | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.624+3768C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547522 | ||||||
| chr10:121547528
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.624+3762C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547528 | ||||||
| chr10:121547820
|
C | T | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.624+3470G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547820 | ||||||
| chr10:121547864
|
G | A | 1 | a0001c0002t0016g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.624+3426C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121547864 | ||||||
| chr10:121548040
|
C | T | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.624+3250G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548040 | ||||||
| chr10:121548107
|
A | C | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+3183T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548107 | ||||||
| chr10:121548209
|
C | G | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0012g0158others(2): Show | 5 | HG01261.hp1 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+3081G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548209 | ||||||
| chr10:121548220
|
T | G | 38 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(35): Show | 38 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.624+3070A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548220 | ||||||
| chr10:121548236
|
G | A | 2 | a0001c0001t0006g0172a0001c0001t0007g0146 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.624+3054C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548236 | ||||||
| chr10:121548245
|
C | CTTTTT | 12 | a0001c0001t0001g0051a0001c0001t0002g0017a0001c0001t0002g0036others(9): Show | 12 | HG01192.hp1 HG01258.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+3040_624+3044d others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTT | 19 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0002g0020others(16): Show | 19 | HG00408.hp2 HG01168.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+3039_624+3044d others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT | 18 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0091others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.624+3038_624+3044d others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0002g0087others(6): Show | 9 | HG00438.hp1 HG01981.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+3037_624+3044d others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0047others(7): Show | 10 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+3036_624+3044d others(11): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0003g0138a0001c0004t0002g0103 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.624+3035_624+3044d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0013g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624+3034_624+3044d others(13): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0032a0001c0002t0002g0035a0001c0002t0007g0164others(1): Show | 4 | HG00408.hp1 HG02165.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+3033_624+3044d others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(6): Show |
2 | a0001c0002t0001g0038a0001c0002t0001g0082 | 2 | HG02523.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.624+3032_624+3044d others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0081 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.624+3031_624+3044d others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0008g0195a0001c0002t0001g0080 | 2 | HG02055.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.624+3030_624+3044d others(17): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0002g0100a0001c0001t0003g0148a0001c0002t0001g0063 | 3 | HG01978.hp2 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.624+3029_624+3044d others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0071a0001c0002t0002g0072a0001c0002t0025g0237 | 3 | HG01978.hp1 HG04115.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.624+3026_624+3044d others(21): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0001g0024 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.624+3021_624+3044d others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
C | CTTTTTTT others(22): Show |
1 | a0001c0002t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+3016_624+3044d others(31): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTT | C | 6 | a0001c0001t0001g0096a0001c0001t0002g0108a0001c0001t0004g0199others(3): Show | 6 | HG00597.hp1 HG01175.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+3041_624+3044d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTT | C | 32 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(29): Show | 32 | HG00438.hp2 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.624+3040_624+3044d others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTT | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.624+3039_624+3044d others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(2): Show |
C | 9 | a0002c0003t0003g0131a0002c0003t0003g0161a0002c0003t0003g0162others(6): Show | 9 | HG01175.hp2 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+3036_624+3044d others(11): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(3): Show |
C | 15 | a0002c0003t0003g0122a0002c0003t0003g0133a0002c0003t0003g0134others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.624+3035_624+3044d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.624+3033_624+3044d others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0001g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624+3032_624+3044d others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0004g0211a0001c0001t0004g0223a0001c0001t0022g0234 | 3 | HG02258.hp2 HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.624+3029_624+3044d others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(11): Show |
C | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0012g0158others(2): Show | 5 | HG01261.hp1 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+3027_624+3044d others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548245
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0004g0230a0001c0001t0018g0013 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.624+3026_624+3044d others(21): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548245 | ||||||
| chr10:121548280
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.624+3010C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548280 | ||||||
| chr10:121548390
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.624+2900G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548390 | ||||||
| chr10:121548546
|
C | T | 13 | a0001c0001t0003g0135a0001c0001t0005g0187a0001c0001t0006g0186others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.624+2744G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548546 | ||||||
| chr10:121548647
|
C | G | 6 | a0001c0001t0005g0187a0001c0001t0006g0186a0001c0002t0002g0079others(3): Show | 6 | HG02630.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+2643G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121548647 | ||||||
| chr10:121549019
|
A | G | 87 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(84): Show | 88 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.624+2271T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549019 | ||||||
| chr10:121549162
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.624+2128A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549162 | ||||||
| chr10:121549236
|
A | C | 1 | a0002c0003t0009g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.624+2054T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549236 | ||||||
| chr10:121549237
|
A | G | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.624+2053T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549237 | ||||||
| chr10:121549462
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.624+1828G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549462 | ||||||
| chr10:121549625
|
G | GCT | 6 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0210others(3): Show | 6 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1663_624+1664d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549625 | ||||||
| chr10:121549707
|
T | G | 11 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0106others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.624+1583A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549707 | ||||||
| chr10:121549746
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.624+1544G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121549746 | ||||||
| chr10:121550198
|
C | T | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+1092G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550198 | ||||||
| chr10:121550230
|
C | T | 86 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.624+1060G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550230 | ||||||
| chr10:121550306
|
A | G | 39 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+984T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550306 | ||||||
| chr10:121550380
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624+910C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550380 | ||||||
| chr10:121550430
|
C | T | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+860G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550430 | ||||||
| chr10:121550433
|
G | A | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.624+857C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550433 | ||||||
| chr10:121550456
|
C | A | 1 | a0001c0001t0002g0088 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.624+834G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550456 | ||||||
| chr10:121550460
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0074a0001c0001t0001g0091others(2): Show | 5 | NA18612.hp2 NA18951.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+830A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550460 | ||||||
| chr10:121550511
|
C | T | 26 | a0002c0003t0002g0114a0002c0003t0003g0122a0002c0003t0003g0131others(23): Show | 26 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.624+779G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550511 | ||||||
| chr10:121550533
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+757C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550533 | ||||||
| chr10:121550534
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+756C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550534 | ||||||
| chr10:121550551
|
A | G | 43 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(40): Show | 43 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.624+739T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550551 | ||||||
| chr10:121550656
|
T | C | 1 | a0001c0001t0002g0059 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.624+634A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550656 | ||||||
| chr10:121550811
|
C | G | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624+479G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550811 | ||||||
| chr10:121550886
|
C | T | 2 | a0001c0001t0004g0223a0001c0001t0022g0234 | 2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.624+404G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121550886 | ||||||
| chr10:121551036
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.624+254G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121551036 | ||||||
| chr10:121551046
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.624+244G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121551046 | ||||||
| chr10:121551136
|
C | T | 1 | a0001c0002t0003g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.624+154G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121551136 | ||||||
| chr10:121551150
|
A | G | 49 | a0001c0001t0004g0211a0001c0001t0009g0010a0001c0001t0009g0011others(46): Show | 49 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.624+140T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121551150 | ||||||
| chr10:121551151
|
T | C | 49 | a0001c0001t0004g0211a0001c0001t0009g0010a0001c0001t0009g0011others(46): Show | 49 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.624+139A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 5/17 | chr10 | 121551151 | ||||||
| chr10:121551540
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.455-81A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551540 | ||||||
| chr10:121551551
|
T | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-92A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551551 | ||||||
| chr10:121551560
|
T | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-101A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551560 | ||||||
| chr10:121551678
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.455-219C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551678 | ||||||
| chr10:121551701
|
C | T | 2 | a0002c0003t0003g0131a0002c0003t0009g0008 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.455-242G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551701 | ||||||
| chr10:121551774
|
A | T | 41 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(38): Show | 41 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.455-315T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551774 | ||||||
| chr10:121551804
|
G | A | 14 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(11): Show | 14 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.455-345C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551804 | ||||||
| chr10:121551996
|
C | A | 25 | a0002c0003t0002g0114a0002c0003t0003g0122a0002c0003t0003g0131others(22): Show | 25 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.455-537G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121551996 | ||||||
| chr10:121552023
|
CA | C | 194 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.455-565delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552023 | ||||||
| chr10:121552023
|
CAA | C | 39 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-566_455-565del others(2): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552023 | ||||||
| chr10:121552028
|
A | C | 2 | a0001c0001t0007g0123a0001c0013t0003g0124 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.455-569T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552028 | ||||||
| chr10:121552089
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.455-630T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552089 | ||||||
| chr10:121552095
|
G | T | 12 | a0001c0001t0003g0135a0001c0001t0005g0187a0001c0001t0006g0186others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-636C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552095 | ||||||
| chr10:121552184
|
G | A | 135 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.455-725C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552184 | ||||||
| chr10:121552400
|
A | G | 2 | a0002c0003t0003g0139a0002c0011t0004g0201 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.455-941T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552400 | ||||||
| chr10:121552460
|
G | A | 65 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0027others(62): Show | 66 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.455-1001C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552460 | ||||||
| chr10:121552577
|
A | T | 1 | a0001c0002t0002g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.455-1118T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552577 | ||||||
| chr10:121552610
|
C | T | 39 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-1151G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552610 | ||||||
| chr10:121552689
|
G | A | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.455-1230C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552689 | ||||||
| chr10:121552967
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.455-1508C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121552967 | ||||||
| chr10:121553364
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-1905G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121553364 | ||||||
| chr10:121553445
|
A | G | 41 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(38): Show | 41 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.455-1986T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121553445 | ||||||
| chr10:121553500
|
A | C | 39 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-2041T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121553500 | ||||||
| chr10:121554016
|
T | C | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.455-2557A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554016 | ||||||
| chr10:121554150
|
T | G | 2 | a0002c0003t0002g0062a0002c0003t0002g0073 | 2 | NA18943.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.455-2691A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554150 | ||||||
| chr10:121554318
|
G | A | 1 | a0001c0001t0008g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.455-2859C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554318 | ||||||
| chr10:121554333
|
C | CT | 5 | a0001c0001t0004g0211a0001c0002t0004g0222a0001c0002t0016g0200others(2): Show | 5 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-2875dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554333 | ||||||
| chr10:121554333
|
C | CTT | 37 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(34): Show | 37 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.455-2876_455-2875d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554333 | ||||||
| chr10:121554505
|
A | AT | 6 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0002g0034others(3): Show | 6 | HG00438.hp1 HG02129.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-3047dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554505 | ||||||
| chr10:121554505
|
AT | A | 84 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.455-3047delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554505 | ||||||
| chr10:121554505
|
ATT | A | 10 | a0001c0001t0009g0012a0001c0002t0003g0130a0001c0002t0004g0209others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-3048_455-3047d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554505 | ||||||
| chr10:121554505
|
ATTTTTTT | A | 39 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-3053_455-3047d others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554505 | ||||||
| chr10:121554540
|
ACAGGGTT others(13): Show |
A | 40 | a0001c0001t0001g0057a0001c0001t0004g0211a0002c0003t0001g0092others(37): Show | 40 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.455-3101_455-3082d others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554540 | ||||||
| chr10:121554660
|
C | T | 39 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(36): Show | 39 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-3201G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554660 | ||||||
| chr10:121554663
|
G | A | 2 | a0001c0002t0008g0224a0001c0004t0003g0127 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.455-3204C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554663 | ||||||
| chr10:121554731
|
T | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-3272A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554731 | ||||||
| chr10:121554860
|
C | T | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.455-3401G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554860 | ||||||
| chr10:121554872
|
A | G | 6 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0210others(3): Show | 6 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-3413T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554872 | ||||||
| chr10:121554910
|
G | A | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.455-3451C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554910 | ||||||
| chr10:121554948
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0002g0086a0001c0001t0002g0094 | 3 | HG01175.hp1 HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.455-3489G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554948 | ||||||
| chr10:121554951
|
G | A | 18 | a0002c0003t0003g0122a0002c0003t0003g0131a0002c0003t0003g0133others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.455-3492C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121554951 | ||||||
| chr10:121555126
|
C | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-3667G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555126 | ||||||
| chr10:121555197
|
A | T | 25 | a0002c0003t0002g0114a0002c0003t0003g0122a0002c0003t0003g0131others(22): Show | 25 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.455-3738T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555197 | ||||||
| chr10:121555371
|
C | CTCAA | 16 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0002g0018others(13): Show | 17 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.455-3916_455-3913d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555371 | ||||||
| chr10:121555371
|
CTCAA | C | 171 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.455-3916_455-3913d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555371 | ||||||
| chr10:121555401
|
C | A | 35 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0114others(32): Show | 35 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.455-3942G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555401 | ||||||
| chr10:121555563
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.455-4104A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555563 | ||||||
| chr10:121555726
|
T | C | 38 | a0001c0001t0004g0211a0002c0003t0001g0092a0002c0003t0002g0062others(35): Show | 38 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.455-4267A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555726 | ||||||
| chr10:121555732
|
C | G | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-4273G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555732 | ||||||
| chr10:121555784
|
G | C | 1 | a0002c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.455-4325C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121555784 | ||||||
| chr10:121556097
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.455-4638G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556097 | ||||||
| chr10:121556102
|
T | TTGGA | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.455-4647_455-4644d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556102 | ||||||
| chr10:121556106
|
A | G | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.455-4647T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556106 | ||||||
| chr10:121556139
|
T | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-4680A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556139 | ||||||
| chr10:121556187
|
T | A | 1 | a0001c0002t0001g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.455-4728A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556187 | ||||||
| chr10:121556209
|
C | T | 2 | a0001c0004t0002g0103a0001c0004t0004g0202 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.455-4750G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556209 | ||||||
| chr10:121556396
|
A | ACT | 34 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0104others(31): Show | 35 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.455-4939_455-4938d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
A | ACTCT | 10 | a0001c0001t0001g0085a0001c0001t0002g0112a0001c0001t0008g0206others(7): Show | 10 | HG01099.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.455-4941_455-4938d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
A | ACTCTCT | 25 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0067others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.455-4943_455-4938d others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
A | ACTCTCTC others(1): Show |
4 | a0001c0001t0006g0185a0001c0001t0017g0007a0001c0001t0019g0136others(1): Show | 4 | HG02027.hp1 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-4945_455-4938d others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
A | ACTCTCTC others(3): Show |
4 | a0001c0001t0002g0048a0001c0001t0012g0158a0001c0005t0008g0231others(1): Show | 4 | HG01261.hp1 HG02027.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4947_455-4938d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
A | ACTCTCTC others(13): Show |
2 | a0001c0001t0004g0199a0002c0006t0006g0193 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.455-4957_455-4938d others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
ACT | A | 101 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.455-4939_455-4938d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
ACTCTCT | A | 3 | a0001c0001t0004g0230a0001c0001t0018g0013a0001c0005t0007g0140 | 3 | HG02257.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.455-4943_455-4938d others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556396
|
ACTCTCTC others(3): Show |
A | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.455-4947_455-4938d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556396 | ||||||
| chr10:121556433
|
C | CTA | 5 | a0002c0003t0002g0114a0002c0003t0003g0161a0002c0003t0003g0162others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-4975_455-4974i others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556433
|
C | CTCTCTA | 4 | a0002c0003t0003g0133a0002c0003t0003g0134a0002c0003t0003g0157others(1): Show | 4 | HG01175.hp2 HG01346.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4975_455-4974i others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556433
|
C | CTCTCTCT others(3): Show |
10 | a0002c0003t0003g0122a0002c0003t0003g0131a0002c0003t0003g0156others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.455-4975_455-4974i others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556433
|
C | CTCTCTCT others(5): Show |
3 | a0001c0001t0009g0010a0001c0001t0009g0011a0002c0003t0004g0233 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.455-4975_455-4974i others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556433
|
C | CTCTCTCT others(7): Show |
2 | a0002c0003t0009g0009a0002c0003t0013g0205 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.455-4975_455-4974i others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556433
|
C | CTCTCTCT others(9): Show |
1 | a0002c0003t0009g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.455-4975_455-4974i others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556433 | ||||||
| chr10:121556726
|
C | T | 1 | a0001c0002t0016g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.455-5267G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556726 | ||||||
| chr10:121556735
|
G | A | 1 | a0001c0001t0004g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.455-5276C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556735 | ||||||
| chr10:121556941
|
C | T | 27 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(24): Show | 27 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.455-5482G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121556941 | ||||||
| chr10:121557443
|
G | A | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.455-5984C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121557443 | ||||||
| chr10:121557498
|
C | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-6039G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121557498 | ||||||
| chr10:121557522
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.455-6063T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121557522 | ||||||
| chr10:121557671
|
T | C | 33 | a0001c0001t0004g0211a0001c0001t0009g0010a0001c0001t0009g0011others(30): Show | 33 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.455-6212A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121557671 | ||||||
| chr10:121557767
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.455-6308A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121557767 | ||||||
| chr10:121558128
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+6374C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558128 | ||||||
| chr10:121558217
|
T | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.454+6285A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558217 | ||||||
| chr10:121558276
|
C | G | 2 | a0002c0003t0003g0131a0002c0003t0009g0008 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.454+6226G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558276 | ||||||
| chr10:121558412
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0046others(2): Show | 5 | HG01433.hp2 HG01496.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+6090G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558412 | ||||||
| chr10:121558422
|
C | G | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454+6080G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558422 | ||||||
| chr10:121558597
|
G | C | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.454+5905C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558597 | ||||||
| chr10:121558603
|
G | GT | 15 | a0002c0003t0003g0122a0002c0003t0003g0131a0002c0003t0003g0133others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.454+5898dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558603 | ||||||
| chr10:121558603
|
G | GTT | 4 | a0001c0004t0004g0202a0002c0003t0003g0134a0002c0003t0010g0002others(1): Show | 4 | HG01175.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+5897_454+5898d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558603 | ||||||
| chr10:121558610
|
G | GT | 25 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0112others(22): Show | 25 | HG00621.hp2 HG00738.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.454+5891dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558610 | ||||||
| chr10:121558610
|
G | T | 19 | a0001c0004t0004g0202a0002c0003t0003g0122a0002c0003t0003g0131others(16): Show | 19 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.454+5892C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558610 | ||||||
| chr10:121558612
|
T | G | 2 | a0001c0001t0004g0230a0001c0001t0018g0013 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454+5890A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558612 | ||||||
| chr10:121558671
|
A | G | 140 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.454+5831T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558671 | ||||||
| chr10:121558739
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454+5763C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558739 | ||||||
| chr10:121558830
|
G | A | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+5672C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558830 | ||||||
| chr10:121558838
|
C | G | 1 | a0002c0003t0016g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.454+5664G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558838 | ||||||
| chr10:121558888
|
T | G | 1 | a0001c0001t0004g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.454+5614A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121558888 | ||||||
| chr10:121559111
|
G | GA | 8 | a0001c0001t0003g0126a0001c0001t0003g0150a0001c0001t0004g0199others(5): Show | 8 | HG00735.hp2 HG01978.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.454+5390dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559111 | ||||||
| chr10:121559111
|
GA | G | 37 | a0001c0001t0002g0045a0001c0001t0003g0129a0001c0001t0005g0180others(34): Show | 37 | HG00558.hp1 HG00621.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.454+5390delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559111 | ||||||
| chr10:121559133
|
A | C | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+5369T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559133 | ||||||
| chr10:121559179
|
G | C | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.454+5323C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559179 | ||||||
| chr10:121559221
|
C | T | 27 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(24): Show | 27 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.454+5281G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559221 | ||||||
| chr10:121559309
|
A | G | 6 | a0001c0001t0003g0135a0001c0001t0023g0235a0001c0002t0003g0145others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+5193T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559309 | ||||||
| chr10:121559361
|
G | C | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+5141C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559361 | ||||||
| chr10:121559420
|
G | A | 2 | a0002c0003t0002g0062a0002c0003t0002g0073 | 2 | NA18943.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.454+5082C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559420 | ||||||
| chr10:121559447
|
A | G | 140 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.454+5055T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121559447 | ||||||
| chr10:121560029
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454+4473C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560029 | ||||||
| chr10:121560100
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.454+4402C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560100 | ||||||
| chr10:121560136
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.454+4366G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560136 | ||||||
| chr10:121560202
|
C | T | 22 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+4300G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560202 | ||||||
| chr10:121560219
|
G | T | 1 | a0001c0002t0003g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454+4283C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560219 | ||||||
| chr10:121560263
|
G | A | 1 | a0001c0013t0003g0124 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.454+4239C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560263 | ||||||
| chr10:121560386
|
G | A | 3 | a0002c0003t0001g0092a0002c0003t0005g0176a0002c0003t0005g0184 | 3 | HG00621.hp2 HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.454+4116C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560386 | ||||||
| chr10:121560397
|
G | A | 78 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0039others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.454+4105C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560397 | ||||||
| chr10:121560528
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.454+3974A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560528 | ||||||
| chr10:121560531
|
C | T | 5 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0210others(2): Show | 5 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+3971G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560531 | ||||||
| chr10:121560593
|
C | G | 2 | a0001c0001t0015g0159a0001c0001t0015g0160 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.454+3909G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560593 | ||||||
| chr10:121560594
|
A | G | 2 | a0001c0001t0015g0159a0001c0001t0015g0160 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.454+3908T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560594 | ||||||
| chr10:121560605
|
A | T | 1 | a0002c0003t0012g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454+3897T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560605 | ||||||
| chr10:121560608
|
C | A | 1 | a0001c0001t0008g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.454+3894G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560608 | ||||||
| chr10:121560615
|
C | CA | 78 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(75): Show | 79 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.454+3886dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
C | CAA | 23 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0002g0048others(20): Show | 23 | HG00735.hp1 HG01261.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.454+3885_454+3886d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
C | CAAA | 14 | a0001c0001t0002g0028a0001c0002t0005g0181a0001c0004t0004g0202others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.454+3884_454+3886d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
C | CAAAA | 5 | a0002c0003t0003g0157a0002c0003t0003g0163a0002c0003t0009g0009others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+3883_454+3886d others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
CA | C | 8 | a0001c0001t0003g0135a0001c0001t0007g0141a0001c0002t0002g0113others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.454+3886delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
CAAA | C | 11 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(8): Show | 11 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+3884_454+3886d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560615
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0015 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.454+3873_454+3886d others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560615 | ||||||
| chr10:121560863
|
C | T | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+3639G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121560863 | ||||||
| chr10:121561191
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.454+3311C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561191 | ||||||
| chr10:121561279
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0126 | 2 | HG00735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.454+3223G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561279 | ||||||
| chr10:121561317
|
A | G | 35 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(32): Show | 35 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.454+3185T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561317 | ||||||
| chr10:121561349
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.454+3153C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561349 | ||||||
| chr10:121561425
|
C | CA | 33 | a0001c0001t0002g0058a0001c0001t0002g0108a0001c0001t0003g0132others(30): Show | 33 | HG00597.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.454+3076dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561425 | ||||||
| chr10:121561432
|
A | C | 22 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+3070T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561432 | ||||||
| chr10:121561554
|
T | C | 2 | a0001c0005t0004g0213a0002c0006t0006g0193 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.454+2948A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561554 | ||||||
| chr10:121561565
|
C | A | 1 | a0001c0001t0002g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.454+2937G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561565 | ||||||
| chr10:121561614
|
G | GA | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+2887dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121561614 | ||||||
| chr10:121562121
|
T | G | 1 | a0001c0001t0002g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.454+2381A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562121 | ||||||
| chr10:121562255
|
ACT | A | 22 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+2245_454+2246d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562255 | ||||||
| chr10:121562284
|
G | T | 1 | a0002c0003t0016g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.454+2218C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562284 | ||||||
| chr10:121562287
|
T | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0036 | 2 | HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.454+2215A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562287 | ||||||
| chr10:121562319
|
C | T | 2 | a0002c0003t0009g0009a0002c0003t0010g0002 | 2 | HG01175.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.454+2183G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562319 | ||||||
| chr10:121562395
|
A | G | 6 | a0001c0002t0003g0130a0001c0002t0004g0209a0001c0002t0004g0210others(3): Show | 6 | HG02109.hp2 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+2107T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562395 | ||||||
| chr10:121562437
|
A | AC | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+2064dupG | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562437 | ||||||
| chr10:121562465
|
A | G | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+2037T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562465 | ||||||
| chr10:121562585
|
C | T | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.454+1917G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562585 | ||||||
| chr10:121562612
|
T | G | 22 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+1890A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562612 | ||||||
| chr10:121562616
|
T | A | 22 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+1886A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562616 | ||||||
| chr10:121562640
|
G | A | 11 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(8): Show | 11 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+1862C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562640 | ||||||
| chr10:121562965
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.454+1537G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562965 | ||||||
| chr10:121562966
|
G | A | 3 | a0001c0001t0012g0158a0001c0001t0017g0007a0001c0005t0008g0231 | 3 | HG01261.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+1536C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121562966 | ||||||
| chr10:121563022
|
T | C | 1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.454+1480A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563022 | ||||||
| chr10:121563045
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454+1457C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563045 | ||||||
| chr10:121563197
|
A | G | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.454+1305T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563197 | ||||||
| chr10:121563346
|
C | G | 2 | a0001c0001t0004g0198a0001c0001t0007g0166 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.454+1156G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563346 | ||||||
| chr10:121563359
|
A | G | 38 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(35): Show | 38 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.454+1143T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563359 | ||||||
| chr10:121563373
|
C | T | 18 | a0001c0001t0003g0135a0001c0004t0004g0202a0002c0003t0003g0122others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.454+1129G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563373 | ||||||
| chr10:121563383
|
T | A | 1 | a0002c0003t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454+1119A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563383 | ||||||
| chr10:121563407
|
G | A | 3 | a0001c0002t0003g0130a0001c0002t0004g0212a0001c0002t0004g0222 | 3 | HG02109.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454+1095C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563407 | ||||||
| chr10:121563500
|
T | C | 50 | a0001c0001t0004g0211a0001c0001t0009g0010a0001c0001t0009g0011others(47): Show | 50 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.454+1002A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563500 | ||||||
| chr10:121563510
|
C | T | 1 | a0001c0002t0003g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.454+992G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563510 | ||||||
| chr10:121563528
|
G | A | 1 | a0002c0003t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.454+974C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563528 | ||||||
| chr10:121563669
|
T | C | 1 | a0001c0004t0002g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.454+833A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121563669 | ||||||
| chr10:121564285
|
C | T | 1 | a0002c0003t0002g0073 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.454+217G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121564285 | ||||||
| chr10:121564295
|
G | A | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.454+207C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121564295 | ||||||
| chr10:121564395
|
C | T | 3 | a0001c0002t0003g0130a0001c0002t0004g0212a0001c0002t0004g0222 | 3 | HG02109.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454+107G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121564395 | ||||||
| chr10:121564448
|
A | G | 41 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0002t0004g0209others(38): Show | 41 | HG00621.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.454+54T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121564448 | ||||||
| chr10:121564487
|
C | T | 1 | a0002c0003t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454+15G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 4/17 | chr10 | 121564487 | ||||||
| chr10:121564663
|
T | C | 1 | a0002c0003t0016g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.377-84A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121564663 | ||||||
| chr10:121564884
|
A | G | 1 | a0001c0001t0003g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.377-305T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121564884 | ||||||
| chr10:121564950
|
A | G | 2 | a0001c0002t0004g0228a0001c0002t0004g0229 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.377-371T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121564950 | ||||||
| chr10:121565033
|
C | T | 1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+405G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565033 | ||||||
| chr10:121565176
|
C | CA | 104 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(101): Show | 104 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.376+261dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565176 | ||||||
| chr10:121565176
|
C | CAA | 32 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0002g0028others(29): Show | 32 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.376+260_376+261dup others(2): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565176 | ||||||
| chr10:121565176
|
C | CAAA | 15 | a0001c0001t0003g0148a0001c0001t0005g0180a0002c0003t0001g0092others(12): Show | 15 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.376+259_376+261dup others(3): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565176 | ||||||
| chr10:121565225
|
T | A | 23 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0004t0004g0202others(20): Show | 23 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.376+213A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565225 | ||||||
| chr10:121565244
|
T | A | 1 | a0002c0003t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.376+194A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565244 | ||||||
| chr10:121565375
|
C | T | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.376+63G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 3/17 | chr10 | 121565375 | ||||||
| chr10:121565730
|
C | T | 3 | a0002c0003t0004g0214a0002c0003t0010g0006a0002c0003t0012g0119 | 3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110-26G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121565730 | ||||||
| chr10:121565758
|
G | A | 13 | a0002c0003t0001g0092a0002c0003t0002g0062a0002c0003t0002g0070others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.110-54C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121565758 | ||||||
| chr10:121565883
|
G | C | 33 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0002g0018others(30): Show | 34 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.110-179C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121565883 | ||||||
| chr10:121565964
|
T | C | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-260A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121565964 | ||||||
| chr10:121566024
|
T | C | 44 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0002g0018others(41): Show | 45 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.110-320A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566024 | ||||||
| chr10:121566150
|
C | G | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110-446G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566150 | ||||||
| chr10:121566241
|
T | C | 145 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.110-537A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566241 | ||||||
| chr10:121566280
|
T | C | 54 | a0001c0001t0001g0095a0001c0001t0002g0110a0001c0001t0008g0206others(51): Show | 55 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.110-576A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566280 | ||||||
| chr10:121566479
|
A | G | 1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110-775T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566479 | ||||||
| chr10:121566793
|
C | T | 1 | a0002c0003t0004g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-1089G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121566793 | ||||||
| chr10:121567132
|
A | G | 132 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0031others(129): Show | 132 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.110-1428T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567132 | ||||||
| chr10:121567260
|
G | A | 5 | a0001c0001t0004g0211a0001c0002t0004g0209a0001c0002t0004g0210others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1556C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567260 | ||||||
| chr10:121567265
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.110-1561C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567265 | ||||||
| chr10:121567514
|
C | G | 113 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0031others(110): Show | 113 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.110-1810G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567514 | ||||||
| chr10:121567527
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0002g0040a0001c0001t0002g0054others(1): Show | 4 | HG01346.hp2 NA18943.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1823C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567527 | ||||||
| chr10:121567679
|
G | C | 85 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0027others(82): Show | 86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.110-1975C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567679 | ||||||
| chr10:121567698
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0002g0040a0001c0001t0002g0054others(1): Show | 4 | HG01346.hp2 NA18943.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1994G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567698 | ||||||
| chr10:121567699
|
G | A | 9 | a0001c0001t0004g0199a0001c0001t0005g0187a0001c0001t0006g0186others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-1995C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567699 | ||||||
| chr10:121567872
|
T | C | 2 | a0001c0001t0012g0158a0001c0005t0008g0231 | 2 | HG01261.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.110-2168A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121567872 | ||||||
| chr10:121568047
|
C | T | 1 | a0002c0003t0009g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-2343G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568047 | ||||||
| chr10:121568172
|
C | T | 8 | a0001c0001t0005g0187a0001c0001t0006g0186a0001c0002t0002g0079others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-2468G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568172 | ||||||
| chr10:121568359
|
G | C | 5 | a0001c0001t0001g0083a0001c0001t0002g0036a0001c0002t0001g0033others(2): Show | 5 | HG01109.hp2 HG01258.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-2655C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568359 | ||||||
| chr10:121568362
|
C | T | 56 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0098others(53): Show | 56 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.110-2658G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568362 | ||||||
| chr10:121568510
|
C | T | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-2806G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568510 | ||||||
| chr10:121568619
|
G | A | 9 | a0001c0001t0001g0098a0002c0003t0001g0092a0002c0003t0002g0070others(6): Show | 9 | HG00544.hp1 HG00621.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-2915C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568619 | ||||||
| chr10:121568780
|
C | T | 2 | a0001c0001t0019g0136a0002c0003t0004g0203 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.110-3076G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568780 | ||||||
| chr10:121568814
|
T | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0104others(20): Show | 23 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-3110A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568814 | ||||||
| chr10:121568924
|
G | A | 14 | a0001c0001t0001g0095a0001c0001t0008g0206a0001c0001t0008g0207others(11): Show | 14 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-3220C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568924 | ||||||
| chr10:121568948
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.110-3244G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121568948 | ||||||
| chr10:121569015
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0014g0117a0001c0001t0014g0118 | 3 | HG00735.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.110-3311G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569015 | ||||||
| chr10:121569199
|
T | TTTTTC | 3 | a0001c0002t0004g0209a0001c0002t0004g0210a0001c0002t0004g0212 | 3 | HG03041.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.110-3500_110-3496d others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569199 | ||||||
| chr10:121569199
|
T | TTTTTCTT others(3): Show |
1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110-3505_110-3496d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569199 | ||||||
| chr10:121569199
|
TTTTTC | T | 98 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0042others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.110-3500_110-3496d others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569199 | ||||||
| chr10:121569199
|
TTTTTCTT others(3): Show |
T | 25 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0104others(22): Show | 25 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.110-3505_110-3496d others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569199 | ||||||
| chr10:121569213
|
TCTTTTCT others(4): Show |
T | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110-3520_110-3510d others(13): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569213 | ||||||
| chr10:121569224
|
C | CT | 8 | a0001c0001t0004g0216a0001c0002t0002g0079a0001c0002t0002g0099others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-3521dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569224 | ||||||
| chr10:121569290
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0006g0192 | 2 | HG00544.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.110-3586C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569290 | ||||||
| chr10:121569352
|
T | C | 202 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.110-3648A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569352 | ||||||
| chr10:121569533
|
T | A | 10 | a0001c0001t0004g0216a0001c0001t0007g0166a0001c0001t0019g0136others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-3829A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569533 | ||||||
| chr10:121569697
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110-3993G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569697 | ||||||
| chr10:121569727
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0006g0192 | 2 | HG00544.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.110-4023T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569727 | ||||||
| chr10:121569765
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.110-4061A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569765 | ||||||
| chr10:121569849
|
A | C | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-4145T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569849 | ||||||
| chr10:121569915
|
T | G | 79 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.110-4211A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569915 | ||||||
| chr10:121569992
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.110-4288C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121569992 | ||||||
| chr10:121570153
|
CCT | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0027others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-4451_110-4450d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570153 | ||||||
| chr10:121570213
|
C | T | 1 | a0002c0003t0002g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.110-4509G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570213 | ||||||
| chr10:121570397
|
G | A | 9 | a0001c0001t0004g0204a0001c0001t0004g0226a0001c0002t0002g0079others(6): Show | 9 | HG01261.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-4693C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570397 | ||||||
| chr10:121570417
|
C | A | 27 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0104others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.110-4713G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570417 | ||||||
| chr10:121570555
|
T | C | 1 | a0001c0001t0007g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.110-4851A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570555 | ||||||
| chr10:121570647
|
A | G | 1 | a0002c0003t0016g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110-4943T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570647 | ||||||
| chr10:121570881
|
C | T | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-5177G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570881 | ||||||
| chr10:121570923
|
C | T | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-5219G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570923 | ||||||
| chr10:121570995
|
C | CT | 22 | a0001c0001t0004g0223a0001c0001t0004g0226a0001c0001t0008g0206others(19): Show | 22 | HG00099.hp1 HG00408.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-5292dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121570995 | ||||||
| chr10:121571014
|
A | G | 21 | a0001c0001t0004g0223a0001c0001t0004g0226a0001c0001t0008g0206others(18): Show | 21 | HG00099.hp1 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-5310T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571014 | ||||||
| chr10:121571027
|
C | T | 64 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(61): Show | 64 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.110-5323G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571027 | ||||||
| chr10:121571110
|
T | C | 29 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.110-5406A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571110 | ||||||
| chr10:121571164
|
A | AT | 35 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0003g0148others(32): Show | 35 | HG00438.hp1 HG01109.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.110-5461dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571164 | ||||||
| chr10:121571182
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.110-5478C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571182 | ||||||
| chr10:121571191
|
T | G | 28 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0003g0148others(25): Show | 28 | HG00438.hp1 HG01109.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.110-5487A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571191 | ||||||
| chr10:121571212
|
A | G | 5 | a0001c0001t0004g0226a0001c0002t0002g0079a0001c0002t0002g0099others(2): Show | 5 | HG01175.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-5508T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571212 | ||||||
| chr10:121571270
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110-5566G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571270 | ||||||
| chr10:121571284
|
C | T | 64 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(61): Show | 64 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.110-5580G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571284 | ||||||
| chr10:121571293
|
C | CT | 3 | a0001c0001t0004g0226a0001c0005t0004g0213a0002c0003t0004g0233 | 3 | HG02965.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.110-5590_110-5589i others(3): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571293 | ||||||
| chr10:121571293
|
C | CTT | 11 | a0001c0001t0008g0207a0001c0001t0008g0208a0001c0001t0015g0160others(8): Show | 11 | HG00099.hp1 HG01081.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-5590_110-5589i others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571293 | ||||||
| chr10:121571293
|
C | CTTT | 9 | a0001c0001t0004g0223a0001c0001t0008g0206a0001c0001t0015g0159others(6): Show | 9 | HG01099.hp1 HG01891.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-5590_110-5589i others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571293 | ||||||
| chr10:121571294
|
C | CT | 20 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(17): Show | 20 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.110-5591dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571294 | ||||||
| chr10:121571294
|
C | CTT | 8 | a0001c0001t0001g0015a0001c0001t0002g0069a0001c0001t0002g0108others(5): Show | 8 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-5592_110-5591d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571294 | ||||||
| chr10:121571294
|
C | T | 25 | a0001c0001t0001g0076a0001c0001t0002g0077a0001c0001t0004g0223others(22): Show | 25 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.110-5590G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571294 | ||||||
| chr10:121571294
|
CT | C | 100 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0027others(97): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.110-5591delA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571294 | ||||||
| chr10:121571294
|
CTT | C | 51 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(48): Show | 51 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-5592_110-5591d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571294 | ||||||
| chr10:121571338
|
T | G | 226 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.110-5634A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571338 | ||||||
| chr10:121571426
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.110-5722C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571426 | ||||||
| chr10:121571455
|
G | A | 2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.110-5751C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571455 | ||||||
| chr10:121571560
|
G | A | 2 | a0001c0001t0004g0204a0001c0012t0024g0236 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110-5856C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571560 | ||||||
| chr10:121571637
|
A | G | 30 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0074others(27): Show | 30 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.110-5933T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571637 | ||||||
| chr10:121571646
|
AC | A | 24 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(21): Show | 24 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.110-5943delG | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571646 | ||||||
| chr10:121571647
|
C | A | 2 | a0001c0001t0007g0165a0002c0003t0010g0002 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.110-5943G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571647 | ||||||
| chr10:121571651
|
C | A | 225 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(222): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.110-5947G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571651 | ||||||
| chr10:121571680
|
G | A | 27 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.110-5976C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571680 | ||||||
| chr10:121571776
|
T | A | 1 | a0001c0002t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.110-6072A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571776 | ||||||
| chr10:121571812
|
G | A | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110-6108C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571812 | ||||||
| chr10:121571846
|
G | C | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110-6142C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571846 | ||||||
| chr10:121571894
|
G | C | 24 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.110-6190C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571894 | ||||||
| chr10:121571952
|
A | AT | 7 | a0001c0001t0003g0135a0001c0001t0005g0187a0001c0001t0006g0186others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-6249_110-6248i others(3): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571952 | ||||||
| chr10:121571953
|
A | T | 60 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(57): Show | 60 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.110-6249T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571953 | ||||||
| chr10:121571954
|
T | A | 67 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(64): Show | 67 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.110-6250A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571954 | ||||||
| chr10:121571954
|
T | TA | 24 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.110-6251dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571954 | ||||||
| chr10:121571955
|
A | T | 28 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0003g0148others(25): Show | 28 | HG00438.hp1 HG01109.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.110-6251T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571955 | ||||||
| chr10:121571981
|
C | A | 60 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(57): Show | 60 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.110-6277G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571981 | ||||||
| chr10:121571993
|
G | T | 24 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.110-6289C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121571993 | ||||||
| chr10:121572104
|
A | C | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.110-6400T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572104 | ||||||
| chr10:121572158
|
GA | G | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.110-6455delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572158 | ||||||
| chr10:121572158
|
GAA | G | 16 | a0001c0001t0002g0044a0001c0001t0003g0153a0001c0001t0006g0173others(13): Show | 16 | HG01168.hp1 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-6456_110-6455d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572158 | ||||||
| chr10:121572176
|
A | T | 84 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.110-6472T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572176 | ||||||
| chr10:121572201
|
G | C | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-6497C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572201 | ||||||
| chr10:121572365
|
A | G | 1 | a0001c0002t0002g0035 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.110-6661T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572365 | ||||||
| chr10:121572392
|
G | A | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-6688C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572392 | ||||||
| chr10:121572443
|
A | G | 6 | a0001c0001t0001g0076a0001c0001t0002g0077a0001c0001t0008g0206others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-6739T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572443 | ||||||
| chr10:121572517
|
G | C | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-6813C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572517 | ||||||
| chr10:121572556
|
G | T | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-6852C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572556 | ||||||
| chr10:121572749
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110-7045A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572749 | ||||||
| chr10:121572752
|
T | A | 1 | a0001c0002t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.110-7048A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572752 | ||||||
| chr10:121572775
|
G | A | 187 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.110-7071C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572775 | ||||||
| chr10:121572838
|
A | G | 86 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.110-7134T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572838 | ||||||
| chr10:121572901
|
T | A | 27 | a0001c0001t0001g0076a0001c0001t0002g0064a0001c0001t0002g0077others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.110-7197A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572901 | ||||||
| chr10:121572989
|
T | C | 3 | a0001c0002t0012g0121a0002c0003t0003g0122a0002c0003t0026g0238 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.110-7285A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121572989 | ||||||
| chr10:121573063
|
C | T | 68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(65): Show | 69 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.110-7359G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573063 | ||||||
| chr10:121573160
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.110-7456C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573160 | ||||||
| chr10:121573224
|
C | T | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110-7520G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573224 | ||||||
| chr10:121573332
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.110-7628G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573332 | ||||||
| chr10:121573542
|
G | T | 2 | a0001c0002t0016g0200a0002c0003t0010g0002 | 2 | HG01175.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.110-7838C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573542 | ||||||
| chr10:121573679
|
A | AG | 111 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0084others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.110-7976dupC | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573679 | ||||||
| chr10:121573758
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.110-8054G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573758 | ||||||
| chr10:121573782
|
G | A | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.110-8078C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573782 | ||||||
| chr10:121573909
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | NA18990.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.110-8205C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573909 | ||||||
| chr10:121573955
|
G | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-8251C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573955 | ||||||
| chr10:121573963
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.110-8259C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121573963 | ||||||
| chr10:121574070
|
G | A | 1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-8366C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574070 | ||||||
| chr10:121574297
|
G | C | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110-8593C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574297 | ||||||
| chr10:121574333
|
G | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-8629C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574333 | ||||||
| chr10:121574356
|
C | G | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-8652G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574356 | ||||||
| chr10:121574483
|
C | T | 75 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.110-8779G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574483 | ||||||
| chr10:121574484
|
G | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-8780C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574484 | ||||||
| chr10:121574486
|
A | G | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.110-8782T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574486 | ||||||
| chr10:121574531
|
A | AAAT | 3 | a0001c0001t0023g0235a0001c0004t0002g0103a0002c0003t0010g0002 | 3 | HG01175.hp2 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-8830_110-8828d others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574531 | ||||||
| chr10:121574531
|
A | T | 1 | a0001c0001t0019g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-8827T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574531 | ||||||
| chr10:121574644
|
A | G | 2 | a0001c0002t0002g0109a0001c0002t0002g0113 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-8940T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574644 | ||||||
| chr10:121574731
|
A | G | 1 | a0002c0003t0003g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.110-9027T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574731 | ||||||
| chr10:121574751
|
T | C | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110-9047A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574751 | ||||||
| chr10:121574865
|
G | T | 1 | a0001c0002t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.110-9161C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574865 | ||||||
| chr10:121574943
|
G | A | 75 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.110-9239C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121574943 | ||||||
| chr10:121575033
|
C | A | 9 | a0001c0001t0002g0069a0002c0003t0002g0070a0002c0003t0005g0176others(6): Show | 9 | HG00408.hp2 HG00621.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-9329G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575033 | ||||||
| chr10:121575085
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | NA18990.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.110-9381C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575085 | ||||||
| chr10:121575349
|
T | C | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.110-9645A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575349 | ||||||
| chr10:121575415
|
G | T | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110-9711C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575415 | ||||||
| chr10:121575416
|
G | A | 67 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0085others(64): Show | 67 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.110-9712C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575416 | ||||||
| chr10:121575450
|
C | T | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-9746G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575450 | ||||||
| chr10:121575494
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(17): Show | 20 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.110-9790C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575494 | ||||||
| chr10:121575576
|
C | T | 6 | a0001c0001t0005g0187a0001c0001t0006g0186a0001c0001t0009g0010others(3): Show | 6 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-9872G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575576 | ||||||
| chr10:121575657
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0002g0020 | 2 | HG00597.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.110-9953C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575657 | ||||||
| chr10:121575729
|
C | G | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.110-10025G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575729 | ||||||
| chr10:121575789
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.110-10085C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575789 | ||||||
| chr10:121575829
|
C | T | 20 | a0001c0001t0002g0069a0001c0001t0002g0075a0001c0001t0004g0198others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.110-10125G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575829 | ||||||
| chr10:121575858
|
AAAAT | A | 116 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0085others(113): Show | 116 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.110-10158_110-1015 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575858 | ||||||
| chr10:121575862
|
T | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-10158A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575862 | ||||||
| chr10:121575997
|
G | A | 1 | a0001c0005t0008g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110-10293C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121575997 | ||||||
| chr10:121576044
|
G | A | 2 | a0001c0001t0023g0235a0001c0004t0002g0103 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-10340C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576044 | ||||||
| chr10:121576116
|
G | A | 17 | a0001c0001t0002g0069a0001c0001t0004g0198a0001c0001t0004g0211others(14): Show | 17 | HG00408.hp2 HG00621.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-10412C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576116 | ||||||
| chr10:121576143
|
C | T | 2 | a0001c0001t0001g0053a0002c0003t0026g0238 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.110-10439G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576143 | ||||||
| chr10:121576233
|
T | G | 3 | a0001c0002t0012g0121a0002c0003t0003g0122a0002c0003t0026g0238 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.110-10529A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576233 | ||||||
| chr10:121576249
|
G | C | 3 | a0001c0002t0012g0121a0002c0003t0003g0122a0002c0003t0026g0238 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.110-10545C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576249 | ||||||
| chr10:121576286
|
A | G | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.110-10582T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576286 | ||||||
| chr10:121576288
|
G | A | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-10584C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576288 | ||||||
| chr10:121576325
|
G | C | 23 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(20): Show | 23 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.110-10621C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576325 | ||||||
| chr10:121576352
|
T | C | 39 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(36): Show | 39 | HG00609.hp2 HG00738.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.110-10648A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576352 | ||||||
| chr10:121576422
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(17): Show | 20 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.110-10718C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576422 | ||||||
| chr10:121576953
|
G | A | 1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110-11249C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576953 | ||||||
| chr10:121576980
|
C | T | 74 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.110-11276G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121576980 | ||||||
| chr10:121577066
|
C | T | 2 | a0001c0001t0023g0235a0001c0004t0002g0103 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-11362G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577066 | ||||||
| chr10:121577086
|
G | A | 1 | a0002c0003t0002g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.110-11382C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577086 | ||||||
| chr10:121577134
|
C | CAAAA | 9 | a0001c0001t0008g0206a0001c0001t0017g0007a0001c0002t0004g0209others(6): Show | 9 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-11434_110-1143 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577134 | ||||||
| chr10:121577134
|
C | CAAAAA | 6 | a0001c0001t0002g0077a0001c0001t0004g0223a0001c0001t0008g0195others(3): Show | 6 | HG00642.hp2 HG02055.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-11435_110-1143 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577134 | ||||||
| chr10:121577134
|
C | CAAAAAA | 13 | a0001c0001t0004g0211a0001c0001t0007g0165a0001c0001t0015g0159others(10): Show | 13 | HG01168.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-11436_110-1143 others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577134 | ||||||
| chr10:121577134
|
C | CAAAAAAA | 6 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0021g0189others(3): Show | 6 | HG00738.hp1 HG01928.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-11437_110-1143 others(11): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577134 | ||||||
| chr10:121577150
|
A | T | 1 | a0001c0004t0004g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.110-11446T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577150 | ||||||
| chr10:121577152
|
A | T | 6 | a0001c0001t0004g0216a0001c0001t0007g0166a0001c0002t0013g0217others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-11448T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577152 | ||||||
| chr10:121577154
|
A | AT | 7 | a0001c0002t0001g0024a0001c0002t0001g0065a0001c0002t0002g0113others(4): Show | 7 | HG00642.hp1 HG01109.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-11451_110-1145 others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577154 | ||||||
| chr10:121577154
|
A | ATAT | 3 | a0001c0001t0001g0083a0001c0001t0002g0036a0001c0001t0002g0048 | 3 | HG01258.hp2 HG01496.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.110-11451_110-1145 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577154 | ||||||
| chr10:121577154
|
A | T | 7 | a0001c0001t0001g0052a0001c0001t0004g0216a0001c0001t0007g0166others(4): Show | 7 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-11450T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577154 | ||||||
| chr10:121577156
|
A | AT | 27 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0030others(24): Show | 27 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.110-11453_110-1145 others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577156 | ||||||
| chr10:121577156
|
A | ATAT | 5 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0009g0012others(2): Show | 5 | HG01346.hp2 HG02004.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-11453_110-1145 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577156 | ||||||
| chr10:121577156
|
A | ATATAT | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0067others(4): Show | 8 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-11453_110-1145 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577156 | ||||||
| chr10:121577156
|
A | ATATATAT | 3 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG01433.hp2 HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.110-11453_110-1145 others(11): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577156 | ||||||
| chr10:121577156
|
A | T | 27 | a0001c0001t0001g0025a0001c0001t0001g0041a0001c0001t0001g0052others(24): Show | 27 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.110-11452T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577156 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(29): Show |
1 | a0001c0005t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(40): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(34): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(23): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0116a0002c0006t0006g0193 | 2 | NA19030.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(33): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(25): Show |
1 | a0001c0005t0004g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(36): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0007g0144a0001c0001t0007g0146 | 2 | HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(33): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0007g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(23): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(18): Show |
1 | a0002c0003t0003g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(29): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0007g0143 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(33): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0006g0192 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0003g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(36): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0003g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(38): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0006g0170a0001c0001t0006g0178 | 2 | HG00609.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(27): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0005g0183 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0075a0001c0001t0027g0239 | 2 | HG00544.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(9): Show |
4 | a0001c0001t0001g0089a0001c0001t0002g0094a0001c0004t0002g0103others(1): Show | 4 | HG01109.hp1 HG02083.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-11455_110-1145 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0020g0179 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0006g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(23): Show |
1 | a0001c0013t0003g0124 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(34): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(36): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(4): Show |
3 | a0002c0003t0003g0156a0002c0003t0003g0157a0002c0003t0005g0184 | 3 | HG01346.hp1 HG02004.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(6): Show |
9 | a0001c0001t0001g0091a0001c0001t0002g0112a0001c0001t0006g0191others(6): Show | 9 | HG01243.hp2 HG02809.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-11455_110-1145 others(17): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(8): Show |
1 | a0001c0002t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(19): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0006g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(21): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0005g0169 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(27): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0090 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0005g0182a0001c0001t0005g0187a0001c0002t0003g0145 | 3 | HG01975.hp2 HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0002g0086a0001c0001t0002g0111a0001c0001t0006g0186 | 3 | HG01993.hp1 HG02723.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0005g0175a0001c0001t0005g0180 | 2 | NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(11): Show |
4 | a0001c0001t0006g0171a0001c0001t0006g0188a0001c0002t0002g0072others(1): Show | 4 | HG02083.hp2 HG02129.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11455_110-1145 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0006g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0006g0172 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.110-11455_110-1145 others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAT others(4): Show |
2 | a0001c0001t0001g0097a0001c0001t0002g0087 | 2 | HG03490.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(15): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAAAT others(10): Show |
1 | a0004c0008t0003g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(21): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AAAAAATA others(3): Show |
1 | a0002c0006t0003g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-11455_110-1145 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | AT | 5 | a0001c0001t0001g0098a0001c0001t0001g0106a0001c0001t0002g0018others(2): Show | 5 | HG00544.hp1 HG02129.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-11455_110-1145 others(5): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | ATATAT | 3 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0004g0199 | 3 | HG00597.hp2 HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.110-11455_110-1145 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577158
|
A | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(87): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.110-11454T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577158 | ||||||
| chr10:121577160
|
T | A | 10 | a0001c0001t0001g0076a0001c0001t0008g0207a0001c0002t0002g0078others(7): Show | 10 | HG00099.hp1 HG01261.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-11456A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577160 | ||||||
| chr10:121577162
|
T | A | 8 | a0001c0001t0001g0076a0001c0001t0008g0207a0001c0002t0002g0078others(5): Show | 8 | HG00099.hp1 HG01261.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-11458A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577162 | ||||||
| chr10:121577164
|
T | A | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-11460A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577164 | ||||||
| chr10:121577170
|
T | TAGAGAGA others(5): Show |
2 | a0001c0001t0007g0166a0001c0002t0001g0063 | 2 | HG01978.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.110-11467_110-1146 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577170 | ||||||
| chr10:121577172
|
T | G | 2 | a0001c0001t0007g0166a0001c0002t0001g0063 | 2 | HG01978.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.110-11468A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577172 | ||||||
| chr10:121577172
|
T | TAGAGAGA others(5): Show |
1 | a0001c0002t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.110-11469_110-1146 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577172 | ||||||
| chr10:121577174
|
T | G | 5 | a0001c0001t0007g0166a0001c0002t0001g0063a0001c0002t0001g0065others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11470A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577174 | ||||||
| chr10:121577174
|
T | TAGAGAG | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0107others(1): Show | 4 | HG01978.hp1 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-11471_110-1147 others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577174 | ||||||
| chr10:121577174
|
T | TAGAGAGA others(1): Show |
4 | a0001c0002t0001g0019a0001c0002t0002g0113a0001c0002t0005g0167others(1): Show | 4 | HG00099.hp2 HG00642.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-11471_110-1147 others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577174 | ||||||
| chr10:121577174
|
T | TAGAGAGA others(5): Show |
3 | a0001c0001t0004g0216a0001c0002t0013g0217a0001c0004t0004g0215 | 3 | HG01884.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.110-11471_110-1147 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577174 | ||||||
| chr10:121577174
|
T | TAGAGAGA others(7): Show |
2 | a0001c0001t0002g0077a0001c0002t0013g0218 | 2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.110-11471_110-1147 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577174 | ||||||
| chr10:121577176
|
T | G | 22 | a0001c0001t0002g0077a0001c0001t0003g0125a0001c0001t0004g0216others(19): Show | 22 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-11472A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577176 | ||||||
| chr10:121577176
|
T | TAGAGAG | 5 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0002g0105others(2): Show | 5 | HG00544.hp1 HG00621.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11473_110-1147 others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577176 | ||||||
| chr10:121577176
|
T | TAGAGAGA others(1): Show |
6 | a0001c0001t0001g0039a0001c0001t0002g0028a0001c0001t0002g0037others(3): Show | 6 | HG01081.hp1 HG02155.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-11473_110-1147 others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577176 | ||||||
| chr10:121577176
|
T | TAGAGAGA others(3): Show |
2 | a0001c0001t0001g0025a0001c0001t0004g0223 | 2 | HG00140.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.110-11473_110-1147 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577176 | ||||||
| chr10:121577176
|
T | TAGAGAGA others(9): Show |
1 | a0002c0003t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110-11473_110-1147 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577176 | ||||||
| chr10:121577178
|
T | G | 45 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0098others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.110-11474A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TACAGAGA others(5): Show |
1 | a0001c0004t0002g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAG | 6 | a0001c0001t0001g0095a0001c0001t0002g0111a0001c0001t0005g0180others(3): Show | 6 | HG01257.hp1 HG03579.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-11478_110-1147 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAG | 20 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0089others(17): Show | 20 | HG01081.hp2 HG01168.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.110-11480_110-1147 others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(1): Show |
23 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(20): Show | 23 | HG00558.hp1 HG00735.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-11482_110-1147 others(12): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(3): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0083a0001c0001t0001g0084others(13): Show | 16 | HG00438.hp2 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.110-11484_110-1147 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(5): Show |
14 | a0001c0001t0001g0051a0001c0001t0001g0067a0001c0001t0001g0097others(11): Show | 14 | HG00544.hp2 HG01109.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-11486_110-1147 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(7): Show |
11 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0002g0054others(8): Show | 12 | HG00597.hp2 HG00738.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-11488_110-1147 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(9): Show |
7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0002g0101others(4): Show | 7 | HG00408.hp1 HG01346.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-11490_110-1147 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(11): Show |
5 | a0001c0001t0001g0016a0001c0001t0002g0018a0001c0001t0002g0059others(2): Show | 5 | HG01993.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11492_110-1147 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(13): Show |
1 | a0002c0003t0005g0190 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.110-11494_110-1147 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(17): Show |
2 | a0001c0001t0001g0015a0001c0002t0016g0200 | 2 | HG00558.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.110-11498_110-1147 others(28): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TAGAGAGA others(19): Show |
1 | a0002c0003t0002g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.110-11500_110-1147 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(3): Show |
1 | a0002c0003t0010g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(5): Show |
4 | a0001c0001t0003g0129a0001c0001t0008g0207a0002c0003t0004g0220others(1): Show | 4 | HG00099.hp1 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11475_110-1147 others(16): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(7): Show |
5 | a0001c0002t0004g0222a0001c0002t0008g0224a0001c0004t0003g0127others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11475_110-1147 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(11): Show |
2 | a0001c0001t0001g0076a0001c0001t0002g0058 | 2 | HG01952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(13): Show |
2 | a0001c0001t0002g0064a0002c0003t0005g0177 | 2 | HG00140.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(17): Show |
2 | a0001c0001t0002g0026a0001c0001t0002g0060 | 2 | HG00738.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(28): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(21): Show |
1 | a0001c0001t0002g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATAGAGA others(29): Show |
1 | a0001c0002t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(40): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATAGA others(3): Show |
1 | a0001c0001t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(14): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATAGA others(7): Show |
1 | a0002c0003t0002g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATAGA others(9): Show |
2 | a0002c0003t0010g0003a0002c0003t0010g0005 | 2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATAGA others(13): Show |
2 | a0001c0001t0001g0074a0001c0001t0002g0034 | 2 | NA18977.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(24): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATAGA others(21): Show |
4 | a0001c0001t0002g0017a0001c0001t0002g0061a0001c0001t0002g0071others(1): Show | 4 | HG01192.hp1 HG02129.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-11475_110-1147 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(7): Show |
1 | a0001c0002t0007g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(18): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(20): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(11): Show |
2 | a0001c0001t0001g0050a0002c0003t0005g0176 | 2 | HG00621.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(15): Show |
1 | a0001c0001t0012g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(17): Show |
4 | a0001c0001t0003g0151a0001c0002t0003g0138a0001c0005t0007g0140others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11475_110-1147 others(28): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(19): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0093 | 2 | HG02486.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(21): Show |
1 | a0002c0003t0003g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(15): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG00735.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(17): Show |
1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(28): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(23): Show |
1 | a0001c0002t0012g0121 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(34): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(25): Show |
2 | a0002c0003t0010g0002a0002c0003t0012g0119 | 2 | HG01175.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(36): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(15): Show |
1 | a0002c0011t0004g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(26): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(19): Show |
4 | a0001c0001t0002g0102a0001c0001t0019g0136a0001c0002t0003g0137others(1): Show | 4 | HG00609.hp1 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11475_110-1147 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(23): Show |
1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(34): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(27): Show |
1 | a0001c0001t0004g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(38): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(39): Show |
2 | a0001c0002t0004g0210a0001c0002t0004g0212 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11475_110-1147 others(50): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(19): Show |
1 | a0002c0003t0003g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(30): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(21): Show |
1 | a0002c0003t0003g0162 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.110-11475_110-1147 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577178
|
T | TATATATA others(49): Show |
1 | a0001c0002t0004g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.110-11475_110-1147 others(60): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577178 | ||||||
| chr10:121577180
|
G | T | 5 | a0001c0001t0001g0115a0001c0001t0004g0226a0001c0001t0004g0230others(2): Show | 5 | HG02922.hp1 HG03486.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11476C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577180 | ||||||
| chr10:121577182
|
G | T | 3 | a0001c0001t0004g0230a0001c0004t0004g0202a0002c0003t0004g0232 | 3 | HG02922.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110-11478C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577182 | ||||||
| chr10:121577184
|
G | T | 3 | a0001c0004t0004g0202a0001c0012t0024g0236a0002c0003t0013g0205 | 3 | HG02559.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-11480C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577184 | ||||||
| chr10:121577185
|
A | G | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-11481T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577185 | ||||||
| chr10:121577186
|
G | T | 1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110-11482C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577186 | ||||||
| chr10:121577187
|
A | AGAGAGAG others(21): Show |
1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110-11484_110-1148 others(32): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577187 | ||||||
| chr10:121577187
|
A | G | 2 | a0001c0002t0012g0121a0002c0003t0003g0122 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.110-11483T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577187 | ||||||
| chr10:121577202
|
G | GAGAGAGA others(11): Show |
1 | a0001c0002t0003g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.110-11499_110-1149 others(22): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577202 | ||||||
| chr10:121577208
|
C | G | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110-11504G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577208 | ||||||
| chr10:121577552
|
T | A | 37 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-11848A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577552 | ||||||
| chr10:121577552
|
T | C | 61 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0085others(58): Show | 61 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.110-11848A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577552 | ||||||
| chr10:121577554
|
C | T | 38 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(35): Show | 38 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.110-11850G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577554 | ||||||
| chr10:121577603
|
C | T | 113 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.110-11899G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577603 | ||||||
| chr10:121577668
|
T | C | 113 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.110-11964A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577668 | ||||||
| chr10:121577821
|
A | G | 115 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(112): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.110-12117T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577821 | ||||||
| chr10:121577987
|
A | C | 1 | a0001c0001t0002g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.110-12283T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121577987 | ||||||
| chr10:121578099
|
C | T | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110-12395G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578099 | ||||||
| chr10:121578195
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.110-12491G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578195 | ||||||
| chr10:121578241
|
TG | T | 233 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.110-12538delC | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578241 | ||||||
| chr10:121578300
|
A | G | 31 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0030others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.110-12596T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578300 | ||||||
| chr10:121578328
|
A | G | 1 | a0001c0002t0002g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.110-12624T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578328 | ||||||
| chr10:121578664
|
C | T | 20 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(17): Show | 20 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.110-12960G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578664 | ||||||
| chr10:121578672
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.110-12968C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578672 | ||||||
| chr10:121578835
|
C | T | 2 | a0001c0005t0004g0213a0002c0006t0006g0193 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.110-13131G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578835 | ||||||
| chr10:121578871
|
T | C | 17 | a0001c0001t0002g0069a0001c0001t0004g0198a0001c0001t0004g0211others(14): Show | 17 | HG00408.hp2 HG00621.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-13167A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578871 | ||||||
| chr10:121578934
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.110-13230A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578934 | ||||||
| chr10:121578958
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0002g0017 | 2 | HG01192.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.110-13254G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578958 | ||||||
| chr10:121578959
|
G | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-13255C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121578959 | ||||||
| chr10:121579038
|
G | A | 37 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-13334C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579038 | ||||||
| chr10:121579064
|
C | T | 2 | a0001c0004t0004g0202a0002c0003t0013g0205 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-13360G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579064 | ||||||
| chr10:121579140
|
G | A | 75 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.110-13436C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579140 | ||||||
| chr10:121579235
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.110-13531C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579235 | ||||||
| chr10:121579402
|
G | A | 2 | a0001c0001t0023g0235a0001c0004t0002g0103 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-13698C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579402 | ||||||
| chr10:121579411
|
T | G | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.110-13707A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579411 | ||||||
| chr10:121579461
|
A | G | 66 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0085others(63): Show | 66 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.110-13757T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579461 | ||||||
| chr10:121579527
|
TTCA | T | 37 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-13826_110-1382 others(7): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579527 | ||||||
| chr10:121579661
|
C | T | 1 | a0001c0001t0004g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-13957G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579661 | ||||||
| chr10:121579690
|
C | A | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110-13986G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579690 | ||||||
| chr10:121579742
|
A | G | 233 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.109+13967T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579742 | ||||||
| chr10:121579799
|
C | A | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+13910G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579799 | ||||||
| chr10:121579800
|
A | G | 2 | a0001c0001t0004g0204a0001c0012t0024g0236 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.109+13909T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579800 | ||||||
| chr10:121579816
|
G | C | 2 | a0001c0004t0004g0202a0002c0003t0013g0205 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+13893C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579816 | ||||||
| chr10:121579841
|
G | A | 19 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(16): Show | 19 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+13868C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579841 | ||||||
| chr10:121579991
|
C | T | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109+13718G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121579991 | ||||||
| chr10:121580008
|
A | G | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+13701T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580008 | ||||||
| chr10:121580024
|
G | A | 3 | a0001c0002t0012g0121a0002c0003t0003g0122a0002c0003t0026g0238 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.109+13685C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580024 | ||||||
| chr10:121580171
|
G | A | 38 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(35): Show | 38 | HG00609.hp2 HG00738.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.109+13538C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580171 | ||||||
| chr10:121580471
|
ATC | A | 236 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.109+13236_109+1323 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580471 | ||||||
| chr10:121580491
|
G | T | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.109+13218C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580491 | ||||||
| chr10:121580593
|
A | G | 37 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.109+13116T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580593 | ||||||
| chr10:121580749
|
G | A | 7 | a0001c0001t0019g0136a0001c0002t0003g0137a0001c0002t0003g0138others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+12960C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580749 | ||||||
| chr10:121580797
|
C | T | 74 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.109+12912G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580797 | ||||||
| chr10:121580800
|
A | G | 37 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.109+12909T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580800 | ||||||
| chr10:121580887
|
G | A | 1 | a0001c0001t0004g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.109+12822C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580887 | ||||||
| chr10:121580917
|
GC | G | 112 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(109): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.109+12791delG | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121580917 | ||||||
| chr10:121581073
|
G | A | 2 | a0001c0001t0002g0069a0002c0003t0002g0070 | 2 | HG00408.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.109+12636C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581073 | ||||||
| chr10:121581119
|
T | C | 230 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.109+12590A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581119 | ||||||
| chr10:121581150
|
G | A | 64 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(61): Show | 64 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.109+12559C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581150 | ||||||
| chr10:121581165
|
G | A | 2 | a0001c0001t0003g0151a0002c0003t0012g0119 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.109+12544C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581165 | ||||||
| chr10:121581310
|
G | A | 39 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.109+12399C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581310 | ||||||
| chr10:121581382
|
G | A | 228 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.109+12327C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581382 | ||||||
| chr10:121581399
|
T | C | 1 | a0001c0001t0007g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.109+12310A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581399 | ||||||
| chr10:121581495
|
CTGGGAGG others(6): Show |
C | 74 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.109+12201_109+1221 others(17): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581495 | ||||||
| chr10:121581565
|
C | T | 1 | a0001c0002t0003g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.109+12144G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581565 | ||||||
| chr10:121581575
|
CA | C | 151 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(148): Show | 151 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.109+12133delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581575 | ||||||
| chr10:121581707
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.109+12002C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581707 | ||||||
| chr10:121581733
|
C | T | 1 | a0001c0001t0007g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.109+11976G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581733 | ||||||
| chr10:121581761
|
T | TA | 17 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0004g0226others(14): Show | 17 | HG00438.hp1 HG00438.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.109+11947dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581761 | ||||||
| chr10:121581761
|
TA | T | 144 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.109+11947delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581761 | ||||||
| chr10:121581761
|
TAA | T | 6 | a0001c0001t0002g0034a0001c0001t0007g0165a0001c0001t0017g0007others(3): Show | 6 | HG00408.hp1 HG01168.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+11946_109+1194 others(6): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581761 | ||||||
| chr10:121581762
|
A | T | 4 | a0001c0001t0003g0135a0001c0001t0004g0223a0002c0003t0003g0133others(1): Show | 4 | HG01884.hp1 HG03209.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+11947T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581762 | ||||||
| chr10:121581763
|
A | T | 15 | a0001c0001t0001g0076a0001c0001t0002g0077a0001c0001t0008g0195others(12): Show | 15 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+11946T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581763 | ||||||
| chr10:121581764
|
A | T | 1 | a0001c0001t0007g0165 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.109+11945T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581764 | ||||||
| chr10:121581818
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0002g0088 | 2 | HG01928.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.109+11891G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581818 | ||||||
| chr10:121581933
|
A | AT | 40 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(37): Show | 40 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.109+11775dupA | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581933 | ||||||
| chr10:121581941
|
T | TTTAA | 14 | a0001c0001t0002g0069a0001c0001t0004g0216a0001c0001t0007g0166others(11): Show | 14 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+11767_109+1176 others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581941 | ||||||
| chr10:121581941
|
T | TTTTAA | 10 | a0001c0001t0002g0075a0001c0001t0004g0198a0001c0001t0004g0211others(7): Show | 10 | HG00544.hp2 HG02258.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+11767_109+1176 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581941 | ||||||
| chr10:121581941
|
T | TTTTTA | 84 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(81): Show | 84 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.109+11767_109+1176 others(9): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581941 | ||||||
| chr10:121581993
|
C | T | 1 | a0002c0003t0005g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109+11716G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121581993 | ||||||
| chr10:121582011
|
A | C | 113 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(110): Show | 113 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.109+11698T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582011 | ||||||
| chr10:121582034
|
A | C | 1 | a0001c0002t0025g0237 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.109+11675T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582034 | ||||||
| chr10:121582049
|
C | T | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+11660G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582049 | ||||||
| chr10:121582114
|
T | C | 8 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0005g0169others(5): Show | 8 | HG02071.hp1 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+11595A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582114 | ||||||
| chr10:121582210
|
G | A | 21 | a0001c0001t0002g0069a0001c0001t0004g0198a0001c0001t0004g0211others(18): Show | 21 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+11499C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582210 | ||||||
| chr10:121582275
|
C | G | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+11434G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582275 | ||||||
| chr10:121582331
|
T | A | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+11378A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582331 | ||||||
| chr10:121582457
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.109+11252C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582457 | ||||||
| chr10:121582592
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.109+11117G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582592 | ||||||
| chr10:121582652
|
G | A | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.109+11057C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582652 | ||||||
| chr10:121582756
|
C | A | 11 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+10953G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582756 | ||||||
| chr10:121582793
|
A | G | 11 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+10916T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582793 | ||||||
| chr10:121582817
|
A | G | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.109+10892T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582817 | ||||||
| chr10:121582958
|
G | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(3): Show | 6 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+10751C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121582958 | ||||||
| chr10:121583053
|
T | C | 89 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(86): Show | 89 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.109+10656A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583053 | ||||||
| chr10:121583193
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0086others(1): Show | 4 | HG01175.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+10516C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583193 | ||||||
| chr10:121583216
|
G | A | 2 | a0001c0001t0003g0125a0001c0001t0003g0126 | 2 | HG00735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.109+10493C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583216 | ||||||
| chr10:121583275
|
C | T | 4 | a0001c0001t0004g0211a0001c0002t0004g0209a0001c0002t0004g0210others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+10434G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583275 | ||||||
| chr10:121583306
|
G | C | 2 | a0001c0004t0004g0202a0002c0003t0013g0205 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+10403C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583306 | ||||||
| chr10:121583327
|
C | T | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.109+10382G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583327 | ||||||
| chr10:121583350
|
G | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(3): Show | 6 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+10359C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583350 | ||||||
| chr10:121583382
|
A | G | 1 | a0002c0003t0004g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.109+10327T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583382 | ||||||
| chr10:121583461
|
C | G | 6 | a0001c0001t0002g0069a0002c0003t0002g0070a0002c0003t0010g0003others(3): Show | 6 | HG00408.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+10248G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583461 | ||||||
| chr10:121583530
|
A | G | 3 | a0001c0002t0002g0079a0001c0002t0002g0099a0002c0003t0016g0225 | 3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.109+10179T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583530 | ||||||
| chr10:121583722
|
G | A | 9 | a0001c0001t0005g0187a0001c0001t0006g0186a0001c0001t0009g0010others(6): Show | 9 | HG02257.hp1 HG02723.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+9987C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583722 | ||||||
| chr10:121583759
|
C | CA | 93 | a0001c0001t0001g0067a0001c0001t0001g0083a0001c0001t0001g0084others(90): Show | 93 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.109+9949dupT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583759 | ||||||
| chr10:121583759
|
C | CAA | 7 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0002g0077others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+9948_109+9949d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583759 | ||||||
| chr10:121583759
|
CA | C | 11 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+9949delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583759 | ||||||
| chr10:121583838
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.109+9871G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583838 | ||||||
| chr10:121583955
|
A | G | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.109+9754T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121583955 | ||||||
| chr10:121584008
|
A | G | 2 | a0002c0003t0010g0003a0002c0003t0010g0004 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.109+9701T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584008 | ||||||
| chr10:121584030
|
A | G | 42 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+9679T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584030 | ||||||
| chr10:121584034
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.109+9675A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584034 | ||||||
| chr10:121584206
|
C | T | 1 | a0001c0001t0014g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+9503G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584206 | ||||||
| chr10:121584216
|
C | G | 22 | a0001c0001t0002g0069a0001c0001t0002g0075a0001c0001t0004g0198others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.109+9493G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584216 | ||||||
| chr10:121584379
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+9330C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584379 | ||||||
| chr10:121584395
|
T | G | 110 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(107): Show | 110 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.109+9314A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584395 | ||||||
| chr10:121584419
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+9290T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584419 | ||||||
| chr10:121584435
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+9274C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584435 | ||||||
| chr10:121584443
|
A | G | 102 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(99): Show | 102 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.109+9266T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584443 | ||||||
| chr10:121584459
|
G | A | 20 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0004g0198others(17): Show | 20 | HG00544.hp2 HG01884.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.109+9250C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584459 | ||||||
| chr10:121584463
|
C | CCCACCCC others(31): Show |
101 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(98): Show | 101 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.109+9245_109+9246i others(40): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584463 | ||||||
| chr10:121584473
|
C | A | 3 | a0001c0001t0004g0204a0001c0001t0023g0235a0001c0004t0002g0103 | 3 | HG02109.hp1 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.109+9236G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584473 | ||||||
| chr10:121584478
|
G | C | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.109+9231C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584478 | ||||||
| chr10:121584499
|
G | A | 2 | a0001c0002t0012g0121a0002c0003t0003g0122 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.109+9210C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584499 | ||||||
| chr10:121584501
|
ACC | A | 3 | a0001c0001t0004g0204a0001c0001t0023g0235a0001c0004t0002g0103 | 3 | HG02109.hp1 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.109+9206_109+9207d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584501 | ||||||
| chr10:121584510
|
G | C | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.109+9199C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584510 | ||||||
| chr10:121584513
|
G | C | 237 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.109+9196C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584513 | ||||||
| chr10:121584514
|
A | ATCCCATA others(31): Show |
1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+9194_109+9195i others(40): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584514 | ||||||
| chr10:121584514
|
A | C | 237 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.109+9195T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584514 | ||||||
| chr10:121584515
|
G | A | 82 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(79): Show | 82 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.109+9194C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584515 | ||||||
| chr10:121584538
|
C | T | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+9171G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584538 | ||||||
| chr10:121584539
|
A | C | 3 | a0001c0004t0004g0202a0001c0005t0008g0231a0002c0003t0013g0205 | 3 | HG01261.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+9170T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584539 | ||||||
| chr10:121584539
|
A | G | 129 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.109+9170T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584539 | ||||||
| chr10:121584553
|
A | C | 105 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(102): Show | 105 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+9156T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584553 | ||||||
| chr10:121584555
|
G | A | 1 | a0001c0001t0004g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+9154C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584555 | ||||||
| chr10:121584578
|
C | T | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+9131G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584578 | ||||||
| chr10:121584579
|
G | A | 1 | a0001c0001t0004g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+9130C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584579 | ||||||
| chr10:121584581
|
A | ACC | 105 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(102): Show | 105 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+9126_109+9127d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584581 | ||||||
| chr10:121584633
|
G | T | 3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.109+9076C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584633 | ||||||
| chr10:121584657
|
A | ACACCCCA others(33): Show |
1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.109+9051_109+9052i others(42): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584657 | ||||||
| chr10:121584657
|
A | ACACCCCA others(33): Show |
80 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(77): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.109+9012_109+9051d others(42): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584657 | ||||||
| chr10:121584657
|
A | ACACCCCA others(659): Show |
1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109+9051_109+9052i others(668): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584657 | ||||||
| chr10:121584657
|
A | G | 105 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0083others(102): Show | 105 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+9052T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584657 | ||||||
| chr10:121584661
|
C | CCCACCCC others(110): Show |
1 | a0001c0001t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109+9047_109+9048i others(119): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584661 | ||||||
| chr10:121584696
|
C | T | 10 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(7): Show | 10 | HG00544.hp1 HG00621.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+9013G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584696 | ||||||
| chr10:121584712
|
C | T | 42 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+8997G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584712 | ||||||
| chr10:121584713
|
A | G | 102 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0001t0001g0084others(99): Show | 102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.109+8996T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584713 | ||||||
| chr10:121584713
|
A | T | 52 | a0001c0001t0001g0076a0001c0001t0001g0098a0001c0001t0001g0104others(49): Show | 52 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.109+8996T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584713 | ||||||
| chr10:121584720
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+8989A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584720 | ||||||
| chr10:121584737
|
A | G | 47 | a0001c0001t0001g0031a0001c0001t0001g0115a0001c0001t0001g0116others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.109+8972T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584737 | ||||||
| chr10:121584741
|
C | CCCACCCC others(108): Show |
42 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+8967_109+8968i others(117): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584741 | ||||||
| chr10:121584752
|
T | C | 147 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0083others(144): Show | 147 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.109+8957A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584752 | ||||||
| chr10:121584760
|
T | C | 1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.109+8949A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584760 | ||||||
| chr10:121584770
|
C | A | 43 | a0001c0001t0001g0031a0001c0001t0001g0115a0001c0001t0001g0116others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.109+8939G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584770 | ||||||
| chr10:121584776
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.109+8933G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584776 | ||||||
| chr10:121584791
|
A | C | 104 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.109+8918T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584791 | ||||||
| chr10:121584800
|
T | C | 49 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(46): Show | 49 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.109+8909A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584800 | ||||||
| chr10:121584802
|
A | AC | 102 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(99): Show | 102 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.109+8906dupG | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584802 | ||||||
| chr10:121584816
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+8893C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584816 | ||||||
| chr10:121584818
|
A | ACC | 3 | a0001c0001t0002g0086a0001c0005t0004g0213a0002c0006t0006g0193 | 3 | HG01993.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.109+8889_109+8890d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584818 | ||||||
| chr10:121584818
|
A | ACCCCACC others(73): Show |
100 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(97): Show | 100 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.109+8890_109+8891i others(82): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584818 | ||||||
| chr10:121584822
|
C | A | 101 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(98): Show | 101 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.109+8887G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(33): Show |
1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.109+8886_109+8887i others(42): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(187): Show |
31 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(28): Show | 31 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.109+8886_109+8887i others(196): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(187): Show |
1 | a0001c0001t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109+8886_109+8887i others(196): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(342): Show |
1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+8886_109+8887i others(351): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(265): Show |
1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109+8886_109+8887i others(274): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(342): Show |
8 | a0001c0001t0004g0226a0001c0001t0004g0230a0001c0002t0004g0228others(5): Show | 8 | HG01243.hp1 HG01261.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+8886_109+8887i others(351): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(342): Show |
79 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.109+8886_109+8887i others(351): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(497): Show |
1 | a0001c0004t0004g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.109+8886_109+8887i others(506): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(891): Show |
1 | a0001c0001t0004g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+8886_109+8887i others(900): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(187): Show |
9 | a0001c0001t0003g0135a0001c0001t0019g0136a0001c0002t0003g0137others(6): Show | 9 | HG01884.hp1 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+8886_109+8887i others(196): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584822
|
C | CCCCAACC others(71): Show |
2 | a0001c0005t0004g0213a0002c0006t0006g0193 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.109+8886_109+8887i others(80): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584822 | ||||||
| chr10:121584854
|
G | GCACCACC others(30): Show |
1 | a0001c0001t0012g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109+8854_109+8855i others(39): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584854 | ||||||
| chr10:121584854
|
G | GCACCACC others(187): Show |
1 | a0002c0003t0003g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.109+8854_109+8855i others(196): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584854 | ||||||
| chr10:121584862
|
C | A | 1 | a0002c0003t0003g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.109+8847G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584862 | ||||||
| chr10:121584870
|
G | A | 1 | a0002c0003t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+8839C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584870 | ||||||
| chr10:121584908
|
C | T | 3 | a0001c0001t0003g0135a0002c0003t0003g0133a0002c0003t0003g0134 | 3 | HG01884.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.109+8801G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584908 | ||||||
| chr10:121584933
|
G | A | 44 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0125others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.109+8776C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584933 | ||||||
| chr10:121584987
|
G | A | 104 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.109+8722C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121584987 | ||||||
| chr10:121585016
|
G | A | 233 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.109+8693C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121585016 | ||||||
| chr10:121585439
|
G | T | 11 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(8): Show | 11 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+8270C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121585439 | ||||||
| chr10:121585774
|
A | C | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+7935T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121585774 | ||||||
| chr10:121585904
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+7805A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121585904 | ||||||
| chr10:121586027
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.109+7682A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586027 | ||||||
| chr10:121586150
|
C | T | 8 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0005g0169others(5): Show | 8 | HG02071.hp1 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+7559G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586150 | ||||||
| chr10:121586263
|
G | A | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+7446C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586263 | ||||||
| chr10:121586272
|
A | T | 1 | a0002c0003t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+7437T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586272 | ||||||
| chr10:121586302
|
G | A | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.109+7407C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586302 | ||||||
| chr10:121586397
|
A | G | 29 | a0001c0001t0001g0076a0001c0001t0002g0075a0001c0001t0002g0077others(26): Show | 29 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.109+7312T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586397 | ||||||
| chr10:121586598
|
G | T | 1 | a0001c0001t0005g0169 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.109+7111C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586598 | ||||||
| chr10:121586602
|
G | A | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.109+7107C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586602 | ||||||
| chr10:121586676
|
A | G | 104 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.109+7033T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586676 | ||||||
| chr10:121586714
|
T | C | 1 | a0001c0001t0012g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109+6995A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586714 | ||||||
| chr10:121586717
|
T | A | 6 | a0001c0001t0002g0069a0002c0003t0002g0070a0002c0003t0010g0003others(3): Show | 6 | HG00408.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+6992A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121586717 | ||||||
| chr10:121587007
|
T | C | 7 | a0001c0001t0004g0216a0001c0001t0007g0166a0001c0002t0013g0217others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+6702A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587007 | ||||||
| chr10:121587260
|
G | A | 6 | a0001c0001t0002g0069a0002c0003t0002g0070a0002c0003t0010g0003others(3): Show | 6 | HG00408.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+6449C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587260 | ||||||
| chr10:121587387
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.109+6322G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587387 | ||||||
| chr10:121587518
|
G | T | 1 | a0001c0001t0023g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.109+6191C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587518 | ||||||
| chr10:121587639
|
A | G | 9 | a0001c0001t0001g0076a0001c0001t0002g0077a0001c0001t0008g0206others(6): Show | 9 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+6070T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587639 | ||||||
| chr10:121587670
|
T | C | 29 | a0001c0001t0001g0076a0001c0001t0002g0075a0001c0001t0002g0077others(26): Show | 29 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.109+6039A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587670 | ||||||
| chr10:121587898
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109+5811T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587898 | ||||||
| chr10:121587952
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.109+5757A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121587952 | ||||||
| chr10:121588142
|
A | G | 168 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(165): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.109+5567T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588142 | ||||||
| chr10:121588153
|
T | C | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+5556A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588153 | ||||||
| chr10:121588237
|
C | T | 1 | a0001c0001t0006g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.109+5472G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588237 | ||||||
| chr10:121588334
|
C | T | 234 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.109+5375G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588334 | ||||||
| chr10:121588349
|
C | T | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+5360G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588349 | ||||||
| chr10:121588361
|
C | T | 54 | a0001c0001t0001g0076a0001c0001t0001g0098a0001c0001t0001g0104others(51): Show | 54 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.109+5348G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588361 | ||||||
| chr10:121588410
|
TA | T | 231 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.109+5298delT | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588410 | ||||||
| chr10:121588430
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.109+5279G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588430 | ||||||
| chr10:121588695
|
T | TGGAGGAT others(8): Show |
104 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.109+5013_109+5014i others(17): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588695 | ||||||
| chr10:121588824
|
G | A | 2 | a0001c0001t0023g0235a0001c0004t0002g0103 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.109+4885C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588824 | ||||||
| chr10:121588833
|
G | A | 1 | a0001c0002t0002g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.109+4876C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588833 | ||||||
| chr10:121588841
|
C | A | 53 | a0001c0001t0001g0076a0001c0001t0001g0098a0001c0001t0001g0104others(50): Show | 53 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.109+4868G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588841 | ||||||
| chr10:121588875
|
T | C | 104 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.109+4834A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121588875 | ||||||
| chr10:121589016
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.109+4693A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589016 | ||||||
| chr10:121589092
|
C | A | 2 | a0001c0001t0003g0151a0002c0003t0012g0119 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.109+4617G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589092 | ||||||
| chr10:121589148
|
T | A | 2 | a0001c0001t0003g0152a0001c0001t0003g0153 | 2 | NA18954.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.109+4561A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589148 | ||||||
| chr10:121589148
|
T | G | 119 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.109+4561A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589148 | ||||||
| chr10:121589388
|
T | C | 119 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.109+4321A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589388 | ||||||
| chr10:121589498
|
C | CTT | 6 | a0001c0001t0004g0198a0001c0001t0007g0165a0001c0001t0008g0195others(3): Show | 6 | HG01168.hp1 HG01257.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+4209_109+4210d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589498 | ||||||
| chr10:121589565
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.109+4144T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589565 | ||||||
| chr10:121589810
|
A | T | 4 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0007g0123others(1): Show | 4 | HG00735.hp2 HG01168.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+3899T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589810 | ||||||
| chr10:121589852
|
T | C | 2 | a0001c0001t0004g0204a0001c0012t0024g0236 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.109+3857A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589852 | ||||||
| chr10:121589959
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.109+3750C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589959 | ||||||
| chr10:121589960
|
C | T | 4 | a0001c0001t0004g0211a0001c0002t0004g0209a0001c0002t0004g0210others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3749G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121589960 | ||||||
| chr10:121590025
|
C | G | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+3684G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590025 | ||||||
| chr10:121590188
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+3521G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590188 | ||||||
| chr10:121590201
|
G | A | 18 | a0001c0001t0002g0075a0001c0001t0004g0198a0001c0001t0004g0211others(15): Show | 18 | HG00544.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.109+3508C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590201 | ||||||
| chr10:121590398
|
T | C | 2 | a0001c0001t0023g0235a0001c0004t0002g0103 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.109+3311A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590398 | ||||||
| chr10:121590527
|
G | A | 6 | a0001c0001t0012g0158a0002c0003t0003g0156a0002c0003t0003g0157others(3): Show | 6 | HG01109.hp1 HG01346.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+3182C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590527 | ||||||
| chr10:121590590
|
C | T | 4 | a0002c0003t0010g0003a0002c0003t0010g0004a0002c0003t0010g0005others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+3119G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590590 | ||||||
| chr10:121590617
|
A | G | 2 | a0001c0002t0012g0121a0002c0003t0003g0122 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.109+3092T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590617 | ||||||
| chr10:121590675
|
G | C | 1 | a0002c0003t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+3034C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590675 | ||||||
| chr10:121590677
|
T | C | 51 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(48): Show | 51 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.109+3032A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590677 | ||||||
| chr10:121590702
|
A | C | 123 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(120): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.109+3007T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590702 | ||||||
| chr10:121590962
|
G | GGCACGCA others(1): Show |
3 | a0001c0001t0002g0075a0001c0001t0006g0191a0001c0001t0006g0192 | 3 | HG00544.hp2 NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.109+2739_109+2746d others(10): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590962 | ||||||
| chr10:121590991
|
A | G | 4 | a0002c0003t0010g0003a0002c0003t0010g0004a0002c0003t0010g0005others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+2718T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121590991 | ||||||
| chr10:121591007
|
G | A | 133 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(130): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.109+2702C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591007 | ||||||
| chr10:121591007
|
GCA | G | 3 | a0001c0001t0001g0030a0001c0001t0002g0028a0001c0001t0002g0029 | 3 | HG02155.hp2 NA18747.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.109+2700_109+2701d others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591007 | ||||||
| chr10:121591009
|
A | G | 121 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(118): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.109+2700T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591009 | ||||||
| chr10:121591011
|
A | ACG | 13 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(10): Show | 13 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+2697_109+2698i others(4): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591011 | ||||||
| chr10:121591011
|
A | T | 3 | a0001c0001t0001g0025a0001c0001t0002g0026a0002c0003t0010g0002 | 3 | HG00140.hp2 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.109+2698T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591011 | ||||||
| chr10:121591011
|
ACTCTCT | A | 20 | a0001c0001t0001g0076a0001c0001t0002g0077a0001c0001t0004g0211others(17): Show | 20 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.109+2692_109+2697d others(8): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591011 | ||||||
| chr10:121591013
|
T | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(10): Show | 13 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+2696A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591013 | ||||||
| chr10:121591352
|
G | A | 1 | a0001c0002t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.109+2357C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591352 | ||||||
| chr10:121591788
|
G | A | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.109+1921C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591788 | ||||||
| chr10:121591810
|
T | C | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.109+1899A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591810 | ||||||
| chr10:121591894
|
C | T | 4 | a0001c0001t0009g0010a0001c0001t0009g0011a0002c0003t0009g0008others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+1815G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121591894 | ||||||
| chr10:121592028
|
T | G | 1 | a0001c0002t0002g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.109+1681A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592028 | ||||||
| chr10:121592115
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.109+1594G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592115 | ||||||
| chr10:121592165
|
C | A | 1 | a0001c0001t0017g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+1544G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592165 | ||||||
| chr10:121592424
|
C | T | 234 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.109+1285G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592424 | ||||||
| chr10:121592466
|
C | T | 4 | a0002c0003t0010g0003a0002c0003t0010g0004a0002c0003t0010g0005others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+1243G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592466 | ||||||
| chr10:121592601
|
G | A | 1 | a0001c0001t0006g0192 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.109+1108C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592601 | ||||||
| chr10:121592616
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.109+1093G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592616 | ||||||
| chr10:121592622
|
C | T | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(124): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.109+1087G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592622 | ||||||
| chr10:121592706
|
C | T | 49 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(46): Show | 49 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.109+1003G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592706 | ||||||
| chr10:121592803
|
A | G | 142 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(139): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.109+906T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592803 | ||||||
| chr10:121592845
|
G | A | 2 | a0002c0003t0003g0161a0002c0003t0003g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+864C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592845 | ||||||
| chr10:121592868
|
G | A | 19 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(16): Show | 19 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+841C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592868 | ||||||
| chr10:121592877
|
C | T | 4 | a0002c0003t0010g0003a0002c0003t0010g0004a0002c0003t0010g0005others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+832G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592877 | ||||||
| chr10:121592973
|
C | T | 1 | a0002c0003t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+736G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121592973 | ||||||
| chr10:121593081
|
T | C | 1 | a0001c0001t0004g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.109+628A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121593081 | ||||||
| chr10:121593534
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.109+175G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121593534 | ||||||
| chr10:121593535
|
G | A | 1 | a0002c0003t0003g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+174C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121593535 | ||||||
| chr10:121593699
|
A | C | 1 | a0002c0003t0010g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+10T>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | 121593699 | ||||||
| chr10:121594064
|
C | T | 1 | a0001c0002t0002g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-150-97G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594064 | ||||||
| chr10:121594099
|
C | T | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-150-132G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594099 | ||||||
| chr10:121594186
|
T | A | 1 | a0002c0003t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-150-219A>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594186 | ||||||
| chr10:121594355
|
C | T | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-150-388G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594355 | ||||||
| chr10:121594356
|
G | A | 2 | a0001c0002t0002g0079a0001c0002t0002g0099 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-150-389C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594356 | ||||||
| chr10:121594489
|
G | A | 11 | a0001c0001t0004g0223a0001c0001t0022g0234a0001c0002t0002g0079others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-150-522C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594489 | ||||||
| chr10:121594627
|
G | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(10): Show | 13 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-150-660C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594627 | ||||||
| chr10:121594646
|
A | G | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-150-679T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594646 | ||||||
| chr10:121594936
|
T | C | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-150-969A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121594936 | ||||||
| chr10:121595015
|
C | T | 12 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(9): Show | 12 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.-150-1048G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595015 | ||||||
| chr10:121595160
|
G | A | 7 | a0001c0001t0017g0007a0002c0003t0010g0002a0002c0003t0010g0003others(4): Show | 7 | HG01175.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150-1193C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595160 | ||||||
| chr10:121595212
|
T | G | 50 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(47): Show | 50 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.-150-1245A>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595212 | ||||||
| chr10:121595239
|
A | G | 1 | a0001c0010t0008g0194 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-150-1272T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595239 | ||||||
| chr10:121595264
|
C | T | 1 | a0002c0003t0012g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-150-1297G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595264 | ||||||
| chr10:121595415
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0002g0020 | 2 | HG00597.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-150-1448T>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595415 | ||||||
| chr10:121595431
|
G | A | 14 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-150-1464C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595431 | ||||||
| chr10:121595437
|
G | C | 14 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0106others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-150-1470C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595437 | ||||||
| chr10:121595678
|
G | A | 2 | a0001c0001t0006g0191a0001c0001t0006g0192 | 2 | NA19011.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-150-1711C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595678 | ||||||
| chr10:121595865
|
G | A | 1 | a0001c0002t0002g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-150-1898C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595865 | ||||||
| chr10:121595906
|
C | A | 1 | a0001c0001t0002g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-150-1939G>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595906 | ||||||
| chr10:121595951
|
G | A | 2 | a0001c0001t0004g0198a0001c0001t0004g0199 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-150-1984C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595951 | ||||||
| chr10:121595996
|
G | C | 1 | a0002c0006t0006g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-151+1966C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121595996 | ||||||
| chr10:121596174
|
T | C | 48 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0129others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.-151+1788A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596174 | ||||||
| chr10:121596195
|
G | T | 6 | a0001c0001t0017g0007a0002c0003t0010g0002a0002c0003t0010g0003others(3): Show | 6 | HG01175.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-151+1767C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596195 | ||||||
| chr10:121596312
|
G | A | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-151+1650C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596312 | ||||||
| chr10:121596328
|
C | G | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-151+1634G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596328 | ||||||
| chr10:121596399
|
G | A | 1 | a0002c0003t0026g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-151+1563C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596399 | ||||||
| chr10:121596413
|
C | T | 31 | a0001c0001t0005g0169a0001c0001t0005g0175a0001c0001t0005g0180others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-151+1549G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596413 | ||||||
| chr10:121596551
|
T | C | 1 | a0001c0001t0002g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-151+1411A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596551 | ||||||
| chr10:121596590
|
A | T | 1 | a0001c0002t0001g0019 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-151+1372T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596590 | ||||||
| chr10:121596661
|
A | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(139): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-151+1301T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596661 | ||||||
| chr10:121596683
|
A | T | 232 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-151+1279T>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596683 | ||||||
| chr10:121596749
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0002g0017a0001c0001t0002g0018others(1): Show | 5 | HG01192.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-151+1213G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121596749 | ||||||
| chr10:121597076
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-151+886C>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597076 | ||||||
| chr10:121597137
|
C | T | 1 | a0001c0012t0024g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-151+825G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597137 | ||||||
| chr10:121597305
|
G | C | 2 | a0001c0001t0014g0117a0001c0001t0014g0118 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-151+657C>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597305 | ||||||
| chr10:121597314
|
G | A | 2 | a0001c0005t0008g0231a0002c0003t0004g0232 | 2 | HG01261.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-151+648C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597314 | ||||||
| chr10:121597424
|
G | A | 31 | a0001c0001t0005g0169a0001c0001t0005g0175a0001c0001t0005g0180others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-151+538C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597424 | ||||||
| chr10:121597475
|
G | A | 31 | a0001c0001t0005g0169a0001c0001t0005g0175a0001c0001t0005g0180others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-151+487C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597475 | ||||||
| chr10:121597543
|
G | A | 1 | a0002c0003t0004g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-151+419C>T | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597543 | ||||||
| chr10:121597696
|
C | T | 6 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0008g0195others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-151+266G>A | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597696 | ||||||
| chr10:121597847
|
T | C | 1 | a0002c0003t0005g0190 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-151+115A>G | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597847 | ||||||
| chr10:121597900
|
C | G | 31 | a0001c0001t0005g0169a0001c0001t0005g0175a0001c0001t0005g0180others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-151+62G>C | FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 1/17 | chr10 | 121597900 |