Item | Value |
---|---|
geneid | 2261 |
ensemblid | ENSG00000068078.20 |
hgncid | 3690 |
symbol | FGFR3 |
name | fibroblast growth factor receptor 3 |
refseq_nuc | NM_000142.5 |
refseq_prot | NP_000133.1 |
ensembl_nuc | ENST00000440486.8 |
ensembl_prot | ENSP00000414914.2 |
mane_status | MANE Select |
chr | chr4 |
start | 1793293 |
end | 1808867 |
strand | + |
ver | v1.2 |
region | chr4:1793293-1808867 |
region5000 | chr4:1788293-1813867 |
regionname0 | FGFR3_chr4_1793293_1808867 |
regionname5000 | FGFR3_chr4_1788293_1813867 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 806 | 365 | 87 | 79 | 141 | 11 | 45 | 100 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0002 | 0/0 | 806 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0003 | 0/0 | 806 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0004 | 0/0 | 806 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0005 | 0/0 | 806 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0006 | 0/0 | 806 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0007 | 0/0 | 806 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0008 | 0/0 | 806 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(801): Show |
chr4 | 1788293 | 1813867 |
a0009 | 0/0 | 132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | MGAPA others(127): Show |
chr4 | 1788293 | 1813867 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2418 | 269 | 52 | 62 | 113 | 8 | 33 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0002 | 0/0 | 2418 | 31 | 0 | 7 | 15 | 3 | 6 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0003 | 0/0 | 2418 | 10 | 9 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0004 | 0/0 | 2418 | 10 | 9 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0005 | 0/0 | 2418 | 7 | 0 | 0 | 7 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0006 | 0/0 | 2418 | 6 | 3 | 2 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0008 | 0/0 | 2418 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0009 | 0/0 | 2418 | 4 | 0 | 3 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0010 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0011 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0012 | 1/0 | 2418 | 3 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0014 | 0/0 | 2418 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0015 | 0/0 | 2418 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0016 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0018 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0020 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0023 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0024 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0025 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0026 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0027 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0028 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0001c0029 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0002c0007 | 0/0 | 2418 | 5 | 0 | 0 | 5 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0003c0013 | 0/0 | 2418 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0004c0031 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0004c0032 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0005c0030 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0006c0021 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0007c0017 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0008c0019 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2413): Show |
chr4 | 1788293 | 1813867 | ||
a0009c0022 | 0/0 | 2416 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | ATGGG others(2411): Show |
chr4 | 1788293 | 1813867 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4299 | 244 | 48 | 61 | 97 | 8 | 29 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0002 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0005 | 0/0 | 4289 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4284): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0007 | 0/0 | 4299 | 3 | 0 | 1 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0009 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0010 | 0/0 | 4301 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0011 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0012 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0014 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0015 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0016 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0017 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0018 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0020 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0021 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0023 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0024 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0026 | 0/0 | 4301 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0001t0027 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0002t0001 | 0/0 | 4299 | 28 | 0 | 6 | 14 | 3 | 5 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0002t0008 | 0/0 | 4299 | 2 | 0 | 1 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0002t0022 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0003t0001 | 0/0 | 4299 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0003t0002 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0003t0003 | 0/0 | 4299 | 7 | 7 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0004t0001 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0004t0002 | 0/0 | 4299 | 5 | 4 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0004t0004 | 0/0 | 4301 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0004t0025 | 0/0 | 4301 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0005t0001 | 0/0 | 4299 | 7 | 0 | 0 | 7 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0006t0001 | 0/0 | 4299 | 3 | 2 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0006t0002 | 0/0 | 4299 | 2 | 1 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0006t0013 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0008t0001 | 0/0 | 4299 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0009t0001 | 0/0 | 4299 | 4 | 0 | 3 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0010t0006 | 0/0 | 4301 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0011t0001 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0012t0004 | 1/0 | 4301 | 3 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4296): Show |
chr4 | 1788293 | 1813867 |
a0001c0014t0001 | 0/0 | 4299 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0015t0001 | 0/0 | 4299 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0016t0005 | 0/0 | 4289 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4284): Show |
chr4 | 1788293 | 1813867 |
a0001c0018t0001 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0020t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0023t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0024t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0025t0001 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0026t0001 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0027t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0028t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0001c0029t0001 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0002c0007t0001 | 0/0 | 4299 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0002c0007t0019 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0003c0013t0001 | 0/0 | 4299 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0004c0031t0002 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0004c0032t0002 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0005c0030t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0006c0021t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0007c0017t0003 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0008c0019t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4294): Show |
chr4 | 1788293 | 1813867 |
a0009c0022t0001 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | AGTGC others(4292): Show |
chr4 | 1788293 | 1813867 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 60 | 1 | 12 | 36 | 4 | 6 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0002 | 0/0 | 25 | 2 | 7 | 13 | 1 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0004 | 0/0 | 9 | 6 | 3 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 7 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0007g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0009g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0015g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0016g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0017g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0018g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0020g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0021g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0026g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0001t0027g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0003 | 0/0 | 9 | 0 | 4 | 3 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0008g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0002t0022g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0002g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0004t0025g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0005t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0006t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0006t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0006t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0006t0013g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0008t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0009t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0009t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0010t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0010t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0010t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0011t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0011t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0012t0004g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0014t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0015t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0016t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0018t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0020t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0023t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0024t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0025t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0026t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0027t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0028t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0001c0029t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0002c0007t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0002c0007t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0003c0013t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0004c0031t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0004c0032t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0005c0030t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0006c0021t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0007c0017t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0008c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
a0009c0022t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00280 | hp2 | a0005 | c0030 | t0001 | g0011 | EUR | FIN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00408 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00423 | hp1 | a0001 | c0001 | t0015 | g0113 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00558 | hp2 | a0001 | c0025 | t0001 | g0001 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00639 | hp1 | a0001 | c0002 | t0008 | g0003 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00673 | hp1 | a0001 | c0029 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00673 | hp2 | a0001 | c0018 | t0001 | g0002 | EAS | CHS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00741 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG00741 | hp2 | a0001 | c0027 | t0001 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01070 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0029 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01167 | hp1 | a0001 | c0014 | t0001 | g0030 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01168 | hp2 | a0001 | c0006 | t0013 | g0109 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01175 | hp1 | a0001 | c0009 | t0001 | g0015 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01243 | hp2 | a0001 | c0023 | t0001 | g0151 | AMR | PUR | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0037 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01891 | hp1 | a0001 | c0012 | t0004 | g0019 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01975 | hp1 | a0001 | c0004 | t0002 | g0017 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01978 | hp1 | a0006 | c0021 | t0001 | g0083 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02055 | hp2 | a0001 | c0008 | t0001 | g0041 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02056 | hp1 | a0001 | c0005 | t0001 | g0098 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02074 | hp2 | a0001 | c0001 | t0016 | g0104 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02129 | hp1 | a0002 | c0007 | t0001 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02155 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | CDX | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02165 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | CDX | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02257 | hp1 | a0001 | c0004 | t0004 | g0131 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02257 | hp2 | a0001 | c0011 | t0001 | g0157 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02280 | hp2 | a0001 | c0011 | t0001 | g0171 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02602 | hp1 | a0001 | c0020 | t0001 | g0022 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02615 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0132 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0127 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02622 | hp2 | a0001 | c0003 | t0003 | g0133 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02647 | hp1 | a0001 | c0014 | t0001 | g0030 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02723 | hp1 | a0001 | c0008 | t0001 | g0001 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02723 | hp2 | a0001 | c0006 | t0002 | g0107 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02735 | hp2 | a0001 | c0009 | t0001 | g0015 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02738 | hp2 | a0001 | c0002 | t0008 | g0172 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02809 | hp1 | a0001 | c0003 | t0003 | g0153 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02886 | hp1 | a0001 | c0011 | t0001 | g0135 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03098 | hp1 | a0001 | c0004 | t0002 | g0126 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03098 | hp2 | a0001 | c0003 | t0003 | g0129 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03139 | hp1 | a0001 | c0004 | t0025 | g0111 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03139 | hp2 | a0007 | c0017 | t0003 | g0110 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0106 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03195 | hp2 | a0001 | c0004 | t0004 | g0034 | AFR | ESN | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0017 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03225 | hp1 | a0001 | c0008 | t0001 | g0001 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0128 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03710 | hp2 | a0008 | c0019 | t0001 | g0001 | SAS | PJL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03834 | hp2 | a0001 | c0015 | t0001 | g0003 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03927 | hp1 | a0001 | c0001 | t0023 | g0001 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03942 | hp1 | a0001 | c0015 | t0001 | g0003 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04115 | hp1 | a0001 | c0028 | t0001 | g0138 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0001 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04184 | hp1 | a0001 | c0024 | t0001 | g0160 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | STU | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18522 | hp1 | a0001 | c0010 | t0006 | g0155 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18522 | hp2 | a0001 | c0010 | t0006 | g0156 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18612 | hp1 | a0001 | c0001 | t0027 | g0028 | EAS | CHB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18906 | hp2 | a0001 | c0012 | t0004 | g0019 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18939 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18941 | hp1 | a0001 | c0016 | t0005 | g0008 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18942 | hp1 | a0002 | c0007 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18949 | hp2 | a0004 | c0032 | t0002 | g0060 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18956 | hp2 | a0001 | c0001 | t0018 | g0051 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18962 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18974 | hp1 | a0009 | c0022 | t0001 | g0162 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18982 | hp1 | a0001 | c0016 | t0005 | g0008 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18986 | hp1 | a0003 | c0013 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18994 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18998 | hp2 | a0001 | c0006 | t0002 | g0059 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18999 | hp1 | a0002 | c0007 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18999 | hp2 | a0003 | c0013 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19000 | hp2 | a0004 | c0031 | t0002 | g0108 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19002 | hp2 | a0001 | c0001 | t0020 | g0102 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19030 | hp2 | a0001 | c0004 | t0002 | g0105 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19059 | hp2 | a0001 | c0001 | t0026 | g0053 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19060 | hp1 | a0002 | c0007 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19060 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19070 | hp1 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19074 | hp1 | a0003 | c0013 | t0001 | g0002 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19081 | hp2 | a0001 | c0002 | t0022 | g0165 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19082 | hp2 | a0001 | c0001 | t0017 | g0071 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19084 | hp2 | a0002 | c0007 | t0019 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19087 | hp2 | a0001 | c0005 | t0001 | g0087 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19088 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0168 | EUR | TSI | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20905 | hp2 | a0001 | c0001 | t0021 | g0004 | SAS | GIH | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02109 | hp2 | a0001 | c0004 | t0001 | g0130 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02559 | hp1 | a0001 | c0004 | t0004 | g0034 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG02559 | hp2 | a0001 | c0010 | t0006 | g0154 | AFR | ACB | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03471 | hp1 | a0001 | c0008 | t0001 | g0001 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | USA | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA20300 | hp2 | a0001 | c0003 | t0003 | g0144 | AFR | USA | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA21309 | hp1 | a0001 | c0026 | t0001 | g0010 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
homoSapiens | grch38p0 | a0001 | c0012 | t0004 | g0019 | REF | REF | FGFR3_chr4_1788293_1813867 | FGFR3 | chr4 | 1788293 | 1813867 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1799298 | G | A | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.154G>A | p.Gly52Ser | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 429/4301 | 154/2421 | 52/806 | chr4 | 1799298 | |||
chr4:1799337 | G | A | 1 | a0002 | 5 | HG02129.hp1 NA18942.hp1 NA18999.hp1 others(2): Show |
missense_variant | MODERATE | c.193G>A | p.Gly65Arg | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 468/4301 | 193/2421 | 65/806 | chr4 | 1799337 | |||
chr4:1799344 | G | A | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.200G>A | p.Gly67Asp | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 475/4301 | 200/2421 | 67/806 | chr4 | 1799344 | |||
chr4:1799491 | G | A | 1 | a0006 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.347G>A | p.Arg116His | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 622/4301 | 347/2421 | 116/806 | chr4 | 1799491 | |||
chr4:1799521 | CAGGTGAG others(24): Show |
C | 1 | a0009 | 1 | NA18974.hp1 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.379_379+30delGGTGA others(26): Show |
p.Asp127fs | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 654/4301 | 379/2421 | 127/806 | INFO_REALIGN_3_PRIME | chr4 | 1799521 | ||
chr4:1801411 | C | G | 1 | a0003 | 3 | NA18986.hp1 NA18999.hp2 NA19074.hp1 |
missense_variant | MODERATE | c.490C>G | p.Leu164Val | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/18 | 765/4301 | 490/2421 | 164/806 | chr4 | 1801411 | |||
chr4:1804902 | C | T | 1 | a0005 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1345C>T | p.Pro449Ser | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/18 | 1620/4301 | 1345/2421 | 449/806 | chr4 | 1804902 | |||
chr4:1804906 | C | T | 1 | a0004 | 2 | NA18949.hp2 NA19000.hp2 |
missense_variant | MODERATE | c.1349C>T | p.Thr450Met | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/18 | 1624/4301 | 1349/2421 | 450/806 | chr4 | 1804906 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1793964 | C | T | 1 | a0004c0032 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.30C>T | p.Leu10Leu | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/18 | 305/4301 | 30/2421 | 10/806 | chr4 | 1793964 | |||
chr4:1799333 | G | A | 1 | a0001c0018 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.189G>A | p.Pro63Pro | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 464/4301 | 189/2421 | 63/806 | chr4 | 1799333 | |||
chr4:1799396 | G | A | 1 | a0001c0020 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.252G>A | p.Ser84Ser | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 527/4301 | 252/2421 | 84/806 | chr4 | 1799396 | |||
chr4:1799492 | C | T | 3 | a0001c0006 a0004c0031 a0004c0032 |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.348C>T | p.Arg116Arg | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/18 | 623/4301 | 348/2421 | 116/806 | chr4 | 1799492 | |||
chr4:1799784 | C | T | 1 | a0001c0009 | 4 | HG00741.hp1 HG01070.hp1 HG01175.hp1 others(1): Show |
synonymous_variant | LOW | c.417C>T | p.Asp139Asp | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/18 | 692/4301 | 417/2421 | 139/806 | chr4 | 1799784 | |||
chr4:1801509 | C | T | 4 | a0001c0006 a0004c0031 a0004c0032 others(1): Show |
9 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(6): Show |
synonymous_variant | LOW | c.588C>T | p.Arg196Arg | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/18 | 863/4301 | 588/2421 | 196/806 | chr4 | 1801509 | |||
chr4:1801524 | T | C | 7 | a0001c0003 a0001c0004 a0001c0006 others(4): Show |
31 | HG01109.hp2 HG01167.hp1 HG01168.hp2 others(28): Show |
synonymous_variant | LOW | c.603T>C | p.Ile201Ile | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/18 | 878/4301 | 603/2421 | 201/806 | chr4 | 1801524 | |||
chr4:1801658 | G | C | 1 | a0001c0010 | 3 | HG02559.hp2 NA18522.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.654G>C | p.Val218Val | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 6/18 | 929/4301 | 654/2421 | 218/806 | chr4 | 1801658 | |||
chr4:1801866 | G | A | 1 | a0001c0023 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.771G>A | p.Ala257Ala | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/18 | 1046/4301 | 771/2421 | 257/806 | chr4 | 1801866 | |||
chr4:1801977 | T | C | 12 | a0001c0002 a0001c0003 a0001c0004 others(9): Show |
69 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(66): Show |
synonymous_variant | LOW | c.882T>C | p.Asn294Asn | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/18 | 1157/4301 | 882/2421 | 294/806 | chr4 | 1801977 | |||
chr4:1803751 | C | T | 1 | a0001c0005 | 7 | HG02056.hp1 HG02155.hp2 NA18962.hp2 others(4): Show |
synonymous_variant | LOW | c.990C>T | p.Thr330Thr | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/18 | 1265/4301 | 990/2421 | 330/806 | chr4 | 1803751 | |||
chr4:1803775 | C | T | 1 | a0001c0024 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.1014C>T | p.Thr338Thr | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/18 | 1289/4301 | 1014/2421 | 338/806 | chr4 | 1803775 | |||
chr4:1804844 | G | A | 1 | a0001c0016 | 2 | NA18941.hp1 NA18982.hp1 |
synonymous_variant | LOW | c.1287G>A | p.Ala429Ala | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/18 | 1562/4301 | 1287/2421 | 429/806 | chr4 | 1804844 | |||
chr4:1804847 | C | T | 1 | a0001c0015 | 2 | HG03834.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.1290C>T | p.Ser430Ser | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/18 | 1565/4301 | 1290/2421 | 430/806 | chr4 | 1804847 | |||
chr4:1804928 | C | T | 1 | a0001c0029 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1371C>T | p.Leu457Leu | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/18 | 1646/4301 | 1371/2421 | 457/806 | chr4 | 1804928 | |||
chr4:1805391 | C | T | 1 | a0001c0028 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1449C>T | p.Phe483Phe | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 11/18 | 1724/4301 | 1449/2421 | 483/806 | chr4 | 1805391 | |||
chr4:1805439 | C | T | 1 | a0001c0027 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1497C>T | p.Ala499Ala | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 11/18 | 1772/4301 | 1497/2421 | 499/806 | chr4 | 1805439 | |||
chr4:1805454 | C | G | 1 | a0001c0026 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1512C>G | p.Thr504Thr | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 11/18 | 1787/4301 | 1512/2421 | 504/806 | chr4 | 1805454 | |||
chr4:1805751 | G | T | 2 | a0001c0011 a0001c0014 |
5 | HG01167.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1647G>T | p.Gly549Gly | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 13/18 | 1922/4301 | 1647/2421 | 549/806 | chr4 | 1805751 | |||
chr4:1806167 | G | A | 30 | a0001c0001 a0001c0002 a0001c0003 others(27): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
synonymous_variant | LOW | c.1953G>A | p.Thr651Thr | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 14/18 | 2228/4301 | 1953/2421 | 651/806 | chr4 | 1806167 | |||
chr4:1806865 | C | G | 1 | a0001c0008 | 4 | HG02055.hp2 HG02723.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.2205C>G | p.Pro735Pro | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 17/18 | 2480/4301 | 2205/2421 | 735/806 | chr4 | 1806865 | |||
chr4:1807172 | C | T | 1 | a0001c0025 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.2331C>T | p.Thr777Thr | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 2606/4301 | 2331/2421 | 777/806 | chr4 | 1807172 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1793349 | G | C | 1 | a0001c0002t0008 | 2 | HG00639.hp1 HG02738.hp2 |
5_prime_UTR_variant | MODIFIER | c.-219G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/18 | 586 | chr4 | 1793349 | ||||||
chr4:1793421 | G | A | 1 | a0001c0001t0011 | 1 | NA18939.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/18 | 514 | chr4 | 1793421 | ||||||
chr4:1793455 | G | A | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/18 | 480 | chr4 | 1793455 | ||||||
chr4:1807298 | A | G | 1 | a0001c0001t0007 | 3 | HG01175.hp2 HG04115.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*36A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 36 | chr4 | 1807298 | ||||||
chr4:1807356 | G | T | 1 | a0001c0001t0027 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 94 | chr4 | 1807356 | ||||||
chr4:1807400 | C | T | 3 | a0001c0001t0026 a0001c0004t0025 a0001c0010t0006 |
5 | HG02559.hp2 HG03139.hp1 NA18522.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*138C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 138 | chr4 | 1807400 | ||||||
chr4:1807400 | CGT | C | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(49): Show |
361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*157delTG | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 156 | INFO_REALIGN_3_PRIME | chr4 | 1807400 | |||||
chr4:1807400 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0005 a0001c0016t0005 |
5 | HG02071.hp1 HG02135.hp1 NA18941.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*146_*157delTGTGTG others(6): Show |
FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 146 | INFO_REALIGN_3_PRIME | chr4 | 1807400 | |||||
chr4:1807402 | T | C | 3 | a0001c0001t0026 a0001c0004t0025 a0001c0010t0006 |
5 | HG02559.hp2 HG03139.hp1 NA18522.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*140T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 140 | chr4 | 1807402 | ||||||
chr4:1807446 | C | T | 2 | a0001c0003t0003 a0007c0017t0003 |
8 | HG02615.hp2 HG02622.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 184 | chr4 | 1807446 | ||||||
chr4:1807464 | G | A | 1 | a0001c0006t0013 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 202 | chr4 | 1807464 | ||||||
chr4:1807473 | C | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 211 | chr4 | 1807473 | ||||||
chr4:1807509 | A | C | 1 | a0001c0001t0023 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 247 | chr4 | 1807509 | ||||||
chr4:1807651 | C | T | 1 | a0001c0002t0022 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*389C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 389 | chr4 | 1807651 | ||||||
chr4:1807679 | C | G | 1 | a0001c0001t0021 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*417C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 417 | chr4 | 1807679 | ||||||
chr4:1807744 | G | A | 1 | a0001c0001t0014 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 482 | chr4 | 1807744 | ||||||
chr4:1807782 | C | T | 1 | a0001c0001t0020 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 520 | chr4 | 1807782 | ||||||
chr4:1807890 | A | G | 1 | a0002c0007t0019 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 628 | chr4 | 1807890 | ||||||
chr4:1808009 | C | T | 1 | a0001c0001t0018 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*747C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 747 | chr4 | 1808009 | ||||||
chr4:1808060 | C | T | 47 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(44): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 798 | chr4 | 1808060 | ||||||
chr4:1808176 | A | G | 1 | a0001c0001t0017 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 914 | chr4 | 1808176 | ||||||
chr4:1808284 | C | T | 1 | a0001c0001t0009 | 2 | HG02630.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1022C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 1022 | chr4 | 1808284 | ||||||
chr4:1808303 | T | C | 1 | a0001c0010t0006 | 3 | HG02559.hp2 NA18522.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 1041 | chr4 | 1808303 | ||||||
chr4:1808376 | A | G | 2 | a0001c0001t0012 a0001c0001t0016 |
2 | HG02074.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1114A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 1114 | chr4 | 1808376 | ||||||
chr4:1808738 | G | T | 1 | a0001c0001t0015 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 18/18 | 1476 | chr4 | 1808738 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1793594 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-103+129C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793594 | |||||||
chr4:1793606 | C | T | 26 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0159 others(23): Show |
45 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-103+141C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793606 | |||||||
chr4:1793652 | G | A | 1 | a0001c0011t0001g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-102-181G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793652 | |||||||
chr4:1793662 | G | A | 1 | a0001c0002t0001g0158 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-102-171G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793662 | |||||||
chr4:1793663 | A | G | 1 | a0001c0002t0001g0158 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-102-170A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793663 | |||||||
chr4:1793715 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0027g0028 |
2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-102-118G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793715 | |||||||
chr4:1793726 | C | G | 1 | a0001c0002t0001g0158 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-102-107C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793726 | |||||||
chr4:1793782 | C | T | 1 | a0001c0004t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-102-51C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793782 | |||||||
chr4:1793830 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
splice_region_variant&intron_variant | LOW | c.-102-3T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 1/17 | chr4 | 1793830 | |||||||
chr4:1794069 | G | A | 2 | a0001c0006t0001g0029 a0001c0006t0001g0106 |
3 | HG01109.hp2 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.109+26G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794069 | |||||||
chr4:1794137 | G | C | 1 | a0001c0014t0001g0030 | 2 | HG01167.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.109+94G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794137 | |||||||
chr4:1794202 | A | T | 1 | a0001c0001t0016g0104 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.109+159A>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794202 | |||||||
chr4:1794217 | T | C | 7 | a0001c0004t0025g0111 a0001c0006t0001g0029 a0001c0006t0001g0106 others(4): Show |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+174T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794217 | |||||||
chr4:1794269 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+226G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794269 | |||||||
chr4:1794321 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.109+278C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794321 | |||||||
chr4:1794333 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0005g0008 others(1): Show |
8 | HG02071.hp1 HG02074.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+290G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794333 | |||||||
chr4:1794340 | C | A | 2 | a0001c0006t0001g0029 a0001c0006t0001g0106 |
3 | HG01109.hp2 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.109+297C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794340 | |||||||
chr4:1794352 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(26): Show |
41 | HG00558.hp1 HG01167.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.109+309C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794352 | |||||||
chr4:1794388 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.109+345G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794388 | |||||||
chr4:1794453 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.109+410G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794453 | |||||||
chr4:1794470 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0136 others(9): Show |
17 | HG00558.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.109+427G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794470 | |||||||
chr4:1794548 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.109+505C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794548 | |||||||
chr4:1794583 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(28): Show |
43 | HG00558.hp1 HG01167.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.109+540C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794583 | |||||||
chr4:1794627 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0040 |
3 | HG01496.hp1 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.109+584G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794627 | |||||||
chr4:1794705 | C | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0159 others(25): Show |
47 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.109+662C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794705 | |||||||
chr4:1794812 | A | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
135 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.109+769A>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794812 | |||||||
chr4:1794875 | C | T | 1 | a0001c0001t0020g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.109+832C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794875 | |||||||
chr4:1794883 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0027g0028 |
2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.109+840C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794883 | |||||||
chr4:1794902 | C | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
60 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.109+859C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794902 | |||||||
chr4:1794909 | G | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(88): Show |
134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.109+866G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794909 | |||||||
chr4:1794977 | G | C | 1 | a0001c0008t0001g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.109+934G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1794977 | |||||||
chr4:1795190 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+1147A>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795190 | |||||||
chr4:1795194 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+1151C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795194 | |||||||
chr4:1795195 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+1152A>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795195 | |||||||
chr4:1795215 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.109+1172G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795215 | |||||||
chr4:1795251 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.109+1208C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795251 | |||||||
chr4:1795252 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.109+1209G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795252 | |||||||
chr4:1795352 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18971.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.109+1309G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795352 | |||||||
chr4:1795395 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.109+1352T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795395 | |||||||
chr4:1795433 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.109+1390C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795433 | |||||||
chr4:1795440 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+1397C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795440 | |||||||
chr4:1795486 | A | G | 1 | a0001c0004t0004g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+1443A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795486 | |||||||
chr4:1795494 | A | ATAAACTT others(9): Show |
1 | a0001c0001t0001g0120 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.109+1452_109+1467d others(18): Show |
FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 1795494 | ||||||
chr4:1795497 | A | C | 1 | a0001c0002t0001g0037 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.109+1454A>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795497 | |||||||
chr4:1795548 | C | T | 7 | a0001c0004t0025g0111 a0001c0006t0001g0029 a0001c0006t0001g0106 others(4): Show |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+1505C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795548 | |||||||
chr4:1795591 | A | G | 1 | a0001c0003t0003g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109+1548A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795591 | |||||||
chr4:1795620 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.109+1577G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795620 | |||||||
chr4:1795631 | G | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0167 others(22): Show |
43 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.109+1588G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795631 | |||||||
chr4:1795633 | G | A | 2 | a0001c0001t0001g0022 a0001c0020t0001g0022 |
2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.109+1590G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795633 | |||||||
chr4:1795657 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+1614G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795657 | |||||||
chr4:1795695 | C | T | 5 | a0001c0003t0003g0153 a0001c0010t0006g0154 a0001c0010t0006g0155 others(2): Show |
6 | HG01167.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1652C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795695 | |||||||
chr4:1795719 | T | A | 1 | a0001c0024t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.109+1676T>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795719 | |||||||
chr4:1795757 | C | G | 92 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
134 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.109+1714C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795757 | |||||||
chr4:1795777 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.109+1734A>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795777 | |||||||
chr4:1795780 | C | T | 1 | a0001c0004t0004g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+1737C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795780 | |||||||
chr4:1795911 | C | A | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.109+1868C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1795911 | |||||||
chr4:1796014 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(88): Show |
133 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.109+1971T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796014 | |||||||
chr4:1796083 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+2040C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796083 | |||||||
chr4:1796125 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
60 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.109+2082G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796125 | |||||||
chr4:1796206 | A | G | 1 | a0001c0002t0008g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.109+2163A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796206 | |||||||
chr4:1796343 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.109+2300C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796343 | |||||||
chr4:1796392 | T | C | 5 | a0001c0006t0001g0029 a0001c0006t0001g0106 a0001c0006t0002g0107 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+2349T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796392 | |||||||
chr4:1796449 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.109+2406C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796449 | |||||||
chr4:1796536 | C | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(26): Show |
41 | HG00558.hp1 HG01167.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.109+2493C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796536 | |||||||
chr4:1796587 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.109+2544T>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796587 | |||||||
chr4:1796629 | G | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0167 others(24): Show |
45 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.109+2586G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796629 | |||||||
chr4:1796957 | C | T | 1 | a0001c0005t0001g0098 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.110-2297C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1796957 | |||||||
chr4:1797005 | G | C | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0123 others(17): Show |
26 | HG01109.hp2 HG01168.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.110-2249G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797005 | |||||||
chr4:1797009 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.110-2245C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797009 | |||||||
chr4:1797059 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.110-2195G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797059 | |||||||
chr4:1797079 | G | C | 1 | a0001c0002t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.110-2175G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797079 | |||||||
chr4:1797099 | C | T | 1 | a0001c0004t0002g0017 | 3 | HG01975.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110-2155C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797099 | |||||||
chr4:1797286 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.110-1968T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797286 | |||||||
chr4:1797392 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110-1862G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797392 | |||||||
chr4:1797429 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110-1825C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797429 | |||||||
chr4:1797575 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.110-1679T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797575 | |||||||
chr4:1797648 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-1606C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797648 | |||||||
chr4:1797676 | TGGCCAGG others(19): Show |
T | 1 | a0001c0001t0001g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.110-1569_110-1544d others(28): Show |
FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 1797676 | ||||||
chr4:1797724 | C | CG | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0054 others(3): Show |
6 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1526dupG | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 1797724 | ||||||
chr4:1797763 | G | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0167 others(17): Show |
33 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.110-1491G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797763 | |||||||
chr4:1797768 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0123 |
3 | HG02630.hp1 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.110-1486G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797768 | |||||||
chr4:1797948 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110-1306G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797948 | |||||||
chr4:1797979 | G | A | 1 | a0001c0003t0001g0124 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.110-1275G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1797979 | |||||||
chr4:1798306 | G | C | 1 | a0001c0006t0002g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.110-948G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798306 | |||||||
chr4:1798344 | A | G | 2 | a0001c0004t0001g0130 a0001c0010t0006g0156 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.110-910A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798344 | |||||||
chr4:1798356 | C | G | 3 | a0001c0003t0003g0132 a0001c0003t0003g0133 a0001c0006t0002g0107 |
3 | HG02615.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.110-898C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798356 | |||||||
chr4:1798359 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.110-895G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798359 | |||||||
chr4:1798378 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.110-876C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798378 | |||||||
chr4:1798378 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.110-876C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798378 | |||||||
chr4:1798396 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0123 a0001c0003t0003g0129 |
4 | HG02630.hp1 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-858C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798396 | |||||||
chr4:1798423 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.110-831C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798423 | |||||||
chr4:1798474 | G | A | 2 | a0001c0001t0001g0012 a0001c0002t0001g0055 |
5 | HG00738.hp1 HG01106.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-780G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798474 | |||||||
chr4:1798477 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG02922.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-777G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798477 | |||||||
chr4:1798542 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0015g0113 others(1): Show |
5 | HG00423.hp1 HG01175.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-712G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798542 | |||||||
chr4:1798590 | C | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0035 others(25): Show |
34 | HG00423.hp2 HG01109.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.110-664C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798590 | |||||||
chr4:1798597 | C | T | 1 | a0001c0005t0001g0087 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.110-657C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798597 | |||||||
chr4:1798624 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110-630G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798624 | |||||||
chr4:1798636 | CTCCT | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0084 others(12): Show |
17 | HG01069.hp2 HG01071.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-611_110-608del others(4): Show |
FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 1798636 | ||||||
chr4:1798646 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.110-608C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798646 | |||||||
chr4:1798656 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.110-598C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798656 | |||||||
chr4:1798706 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.110-548G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798706 | |||||||
chr4:1798780 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18945.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.110-474C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798780 | |||||||
chr4:1798791 | C | G | 4 | a0001c0003t0003g0127 a0001c0003t0003g0129 a0001c0003t0003g0139 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-463C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798791 | |||||||
chr4:1798792 | C | A | 4 | a0001c0003t0003g0127 a0001c0003t0003g0129 a0001c0003t0003g0139 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-462C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798792 | |||||||
chr4:1798886 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.110-368T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1798886 | |||||||
chr4:1799036 | C | T | 1 | a0001c0004t0002g0017 | 3 | HG01975.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110-218C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1799036 | |||||||
chr4:1799090 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110-164C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1799090 | |||||||
chr4:1799095 | G | A | 2 | a0001c0003t0003g0139 a0001c0003t0003g0144 |
2 | NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.110-159G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1799095 | |||||||
chr4:1799203 | C | T | 2 | a0001c0003t0003g0127 a0001c0003t0003g0129 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.110-51C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 2/17 | chr4 | 1799203 | |||||||
chr4:1799646 | G | C | 7 | a0001c0006t0001g0029 a0001c0006t0001g0106 a0001c0006t0002g0059 others(4): Show |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.380-101G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/17 | chr4 | 1799646 | |||||||
chr4:1799742 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | splice_region_variant&intron_variant | LOW | c.380-5T>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 3/17 | chr4 | 1799742 | |||||||
chr4:1799815 | A | G | 25 | a0001c0003t0001g0124 a0001c0003t0002g0128 a0001c0003t0003g0127 others(22): Show |
30 | HG01109.hp2 HG01167.hp1 HG01168.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.445+3A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799815 | |||||||
chr4:1799828 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445+16A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799828 | |||||||
chr4:1799843 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.445+31C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799843 | |||||||
chr4:1799862 | A | T | 1 | a0001c0023t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445+50A>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799862 | |||||||
chr4:1799890 | C | T | 3 | a0001c0010t0006g0154 a0001c0010t0006g0155 a0001c0010t0006g0156 |
3 | HG02559.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.445+78C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799890 | |||||||
chr4:1799935 | A | G | 2 | a0001c0001t0001g0081 a0001c0028t0001g0138 |
2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.445+123A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799935 | |||||||
chr4:1799970 | T | C | 25 | a0001c0003t0001g0124 a0001c0003t0002g0128 a0001c0003t0003g0127 others(22): Show |
30 | HG01109.hp2 HG01167.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.445+158T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1799970 | |||||||
chr4:1800133 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.445+321G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800133 | |||||||
chr4:1800139 | C | T | 21 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0037 others(18): Show |
36 | HG00639.hp1 HG00738.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.445+327C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800139 | |||||||
chr4:1800167 | A | G | 8 | a0001c0003t0001g0124 a0001c0003t0002g0128 a0001c0004t0001g0130 others(5): Show |
11 | HG01255.hp1 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+355A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800167 | |||||||
chr4:1800198 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.445+386C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800198 | |||||||
chr4:1800240 | CAGGGTGG others(8): Show |
C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0145 a0001c0001t0001g0152 |
4 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+440_445+454del others(15): Show |
FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 1800240 | ||||||
chr4:1800318 | G | A | 2 | a0001c0010t0006g0154 a0001c0010t0006g0156 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445+506G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800318 | |||||||
chr4:1800484 | T | C | 21 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0037 others(18): Show |
36 | HG00639.hp1 HG00738.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.445+672T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800484 | |||||||
chr4:1800551 | A | G | 48 | a0001c0001t0001g0032 a0001c0002t0001g0003 a0001c0002t0001g0007 others(45): Show |
69 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.445+739A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800551 | |||||||
chr4:1800592 | C | T | 7 | a0001c0006t0001g0029 a0001c0006t0001g0106 a0001c0006t0002g0059 others(4): Show |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-775C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800592 | |||||||
chr4:1800823 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.446-544C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800823 | |||||||
chr4:1800884 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.446-483T>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800884 | |||||||
chr4:1800970 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.446-397G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1800970 | |||||||
chr4:1801175 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.446-192G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1801175 | |||||||
chr4:1801177 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.446-190C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1801177 | |||||||
chr4:1801230 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.446-137C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1801230 | |||||||
chr4:1801241 | C | T | 3 | a0001c0010t0006g0154 a0001c0010t0006g0155 a0001c0010t0006g0156 |
3 | HG02559.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.446-126C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1801241 | |||||||
chr4:1801257 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.446-110A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 4/17 | chr4 | 1801257 | |||||||
chr4:1801542 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0064 |
5 | NA18942.hp2 NA18990.hp1 NA19079.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.615+6C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/17 | chr4 | 1801542 | |||||||
chr4:1801544 | C | G | 8 | a0001c0003t0001g0149 a0001c0003t0003g0127 a0001c0003t0003g0129 others(5): Show |
9 | HG01167.hp1 HG02109.hp1 HG02622.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.615+8C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/17 | chr4 | 1801544 | |||||||
chr4:1801545 | G | A | 1 | a0001c0002t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.615+9G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/17 | chr4 | 1801545 | |||||||
chr4:1801580 | T | C | 55 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0147 others(52): Show |
75 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.616-40T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/17 | chr4 | 1801580 | |||||||
chr4:1801605 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.616-15C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 5/17 | chr4 | 1801605 | |||||||
chr4:1801764 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.739+21C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 6/17 | chr4 | 1801764 | |||||||
chr4:1802097 | C | G | 49 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0037 others(46): Show |
69 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.930+72C>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802097 | |||||||
chr4:1802199 | T | C | 9 | a0001c0004t0025g0111 a0001c0006t0001g0029 a0001c0006t0001g0106 others(6): Show |
10 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.930+174T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802199 | |||||||
chr4:1802205 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.930+180G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802205 | |||||||
chr4:1802243 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0037 others(30): Show |
49 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.930+218G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802243 | |||||||
chr4:1802267 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+242A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802267 | |||||||
chr4:1802273 | C | T | 1 | a0001c0006t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.930+248C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802273 | |||||||
chr4:1802293 | G | A | 1 | a0001c0004t0025g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.930+268G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802293 | |||||||
chr4:1802313 | C | T | 2 | a0001c0002t0001g0166 a0009c0022t0001g0162 |
2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.930+288C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802313 | |||||||
chr4:1802362 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.930+337C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802362 | |||||||
chr4:1802525 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.930+500C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802525 | |||||||
chr4:1802549 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(16): Show |
39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.930+524G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802549 | |||||||
chr4:1802578 | G | A | 1 | a0001c0004t0025g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.930+553G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802578 | |||||||
chr4:1802615 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.930+590C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802615 | |||||||
chr4:1802616 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.930+591G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802616 | |||||||
chr4:1802650 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.930+625G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802650 | |||||||
chr4:1802739 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.930+714C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802739 | |||||||
chr4:1802740 | G | T | 2 | a0001c0001t0005g0008 a0001c0016t0005g0008 |
5 | HG02071.hp1 HG02135.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+715G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802740 | |||||||
chr4:1802855 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.930+830C>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802855 | |||||||
chr4:1802863 | C | T | 1 | a0001c0002t0022g0165 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.931-829C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802863 | |||||||
chr4:1802924 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.931-768G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1802924 | |||||||
chr4:1803024 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.931-668C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803024 | |||||||
chr4:1803121 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0076 a0001c0001t0026g0053 |
3 | NA18974.hp2 NA19059.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.931-571C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803121 | |||||||
chr4:1803122 | G | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0125 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.931-570G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803122 | |||||||
chr4:1803222 | C | T | 3 | a0001c0001t0001g0145 a0001c0006t0001g0029 a0001c0006t0001g0106 |
4 | HG01109.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-470C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803222 | |||||||
chr4:1803272 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.931-420G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803272 | |||||||
chr4:1803307 | C | T | 1 | a0001c0023t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.931-385C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803307 | |||||||
chr4:1803403 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.931-289C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803403 | |||||||
chr4:1803425 | G | A | 1 | a0001c0002t0022g0165 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.931-267G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803425 | |||||||
chr4:1803432 | C | T | 1 | a0001c0003t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-260C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803432 | |||||||
chr4:1803569 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.931-123G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803569 | |||||||
chr4:1803684 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18956.hp1 | splice_region_variant&intron_variant | LOW | c.931-8C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 7/17 | chr4 | 1803684 | |||||||
chr4:1803841 | C | T | 6 | a0001c0006t0001g0029 a0001c0006t0001g0106 a0001c0006t0002g0107 others(3): Show |
7 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1075+5C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1803841 | |||||||
chr4:1803866 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0080 a0001c0001t0001g0093 others(1): Show |
7 | HG01069.hp1 HG01261.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+30G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1803866 | |||||||
chr4:1803945 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1075+109G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1803945 | |||||||
chr4:1804021 | G | A | 7 | a0001c0006t0001g0029 a0001c0006t0001g0106 a0001c0006t0002g0059 others(4): Show |
8 | HG01109.hp2 HG01168.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075+185G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804021 | |||||||
chr4:1804072 | T | C | 6 | a0001c0004t0002g0017 a0001c0004t0002g0105 a0001c0004t0002g0126 others(3): Show |
9 | HG01975.hp1 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075+236T>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804072 | |||||||
chr4:1804279 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0125 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1076-51G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804279 | |||||||
chr4:1804285 | T | TG | 19 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0064 others(16): Show |
20 | HG01261.hp1 HG01978.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076-34dupG | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 1804285 | ||||||
chr4:1804285 | TG | T | 23 | a0001c0001t0001g0069 a0001c0002t0001g0003 a0001c0002t0001g0007 others(20): Show |
38 | HG00639.hp1 HG00738.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1076-34delG | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 1804285 | ||||||
chr4:1804286 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1076-44G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804286 | |||||||
chr4:1804288 | G | C | 1 | a0001c0004t0025g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1076-42G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804288 | |||||||
chr4:1804289 | G | C | 2 | a0001c0004t0002g0105 a0001c0004t0002g0126 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1076-41G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804289 | |||||||
chr4:1804294 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1076-36G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804294 | |||||||
chr4:1804313 | C | T | 4 | a0001c0004t0002g0017 a0001c0004t0002g0105 a0001c0004t0002g0126 others(1): Show |
6 | HG01975.hp1 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-17C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804313 | |||||||
chr4:1804314 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1076-16G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804314 | |||||||
chr4:1804317 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1076-13C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 8/17 | chr4 | 1804317 | |||||||
chr4:1804584 | C | T | 3 | a0001c0011t0001g0157 a0001c0011t0001g0171 a0001c0014t0001g0030 |
4 | HG01167.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+64C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 9/17 | chr4 | 1804584 | |||||||
chr4:1804654 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1266+134C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 9/17 | chr4 | 1804654 | |||||||
chr4:1804792 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1267-32C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 9/17 | chr4 | 1804792 | |||||||
chr4:1805019 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1412+50G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805019 | |||||||
chr4:1805045 | C | T | 2 | a0001c0001t0001g0088 a0001c0023t0001g0151 |
2 | HG01243.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1412+76C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805045 | |||||||
chr4:1805089 | T | G | 1 | a0001c0001t0026g0053 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1412+120T>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805089 | |||||||
chr4:1805107 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1412+138G>C | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805107 | |||||||
chr4:1805107 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1412+138G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805107 | |||||||
chr4:1805202 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1413-153C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805202 | |||||||
chr4:1805203 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1413-152G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805203 | |||||||
chr4:1805326 | A | G | 7 | a0001c0003t0003g0127 a0001c0003t0003g0129 a0001c0003t0003g0132 others(4): Show |
7 | HG02615.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-29A>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 10/17 | chr4 | 1805326 | |||||||
chr4:1805551 | G | T | 1 | a0001c0004t0025g0111 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.1535-8G>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 11/17 | chr4 | 1805551 | |||||||
chr4:1805677 | C | CG | 8 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0167 others(5): Show |
8 | HG00735.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1645+10dupG | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 1805677 | ||||||
chr4:1805684 | G | A | 2 | a0001c0003t0003g0127 a0001c0003t0003g0129 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1645+15G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 12/17 | chr4 | 1805684 | |||||||
chr4:1805984 | C | T | 2 | a0001c0004t0002g0105 a0001c0004t0002g0126 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1836+44C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 13/17 | chr4 | 1805984 | |||||||
chr4:1806195 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0065 |
9 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959+22G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 14/17 | chr4 | 1806195 | |||||||
chr4:1806244 | C | T | 1 | a0001c0006t0002g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1960-13C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 14/17 | chr4 | 1806244 | |||||||
chr4:1806489 | C | T | 1 | a0001c0004t0025g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2031-57C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 15/17 | chr4 | 1806489 | |||||||
chr4:1806786 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2169-43G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 16/17 | chr4 | 1806786 | |||||||
chr4:1806788 | C | T | 9 | a0001c0003t0002g0128 a0001c0006t0002g0059 a0001c0006t0002g0107 others(6): Show |
9 | HG01168.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2169-41C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 16/17 | chr4 | 1806788 | |||||||
chr4:1806966 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0082 |
3 | NA18966.hp1 NA18998.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2274+32C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 17/17 | chr4 | 1806966 | |||||||
chr4:1806986 | G | A | 1 | a0001c0001t0018g0051 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2274+52G>A | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 17/17 | chr4 | 1806986 | |||||||
chr4:1807047 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2275-69C>T | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 17/17 | chr4 | 1807047 | |||||||
chr4:1807048 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2275-68T>G | FGFR3 | ENSG00000068078.20 | transcript | ENST00000440486.8 | protein_coding | 17/17 | chr4 | 1807048 |