ClinVar Miner

List of variants in gene FGFR3 reported as not provided

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Total variants: 25
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HGVS dbSNP
NM_000142.4(FGFR3):c.1031C>T (p.Ser344Phe) rs199702395
NM_000142.4(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.4(FGFR3):c.1262G>A (p.Arg421Gln) rs587778355
NM_000142.4(FGFR3):c.130G>A (p.Gly44Ser) rs146080119
NM_000142.4(FGFR3):c.1331C>T (p.Ser444Phe)
NM_000142.4(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.4(FGFR3):c.1349C>T (p.Thr450Met) rs56240927
NM_000142.4(FGFR3):c.1486A>G (p.Lys496Glu) rs587778359
NM_000142.4(FGFR3):c.1559C>T (p.Ser520Leu) rs587778356
NM_000142.4(FGFR3):c.169G>A (p.Val57Met) rs61735064
NM_000142.4(FGFR3):c.1765C>G (p.Leu589Val) rs587778357
NM_000142.4(FGFR3):c.184C>G (p.Pro62Ala) rs533866031
NM_000142.4(FGFR3):c.1887C>T (p.Asn629=) rs104886004
NM_000142.4(FGFR3):c.1908C>G (p.Phe636Leu) rs104886005
NM_000142.4(FGFR3):c.1935C>T (p.Leu645=) rs104886006
NM_000142.4(FGFR3):c.193G>A (p.Gly65Arg) rs2305178
NM_000142.4(FGFR3):c.2129G>T (p.Gly710Val) rs104886023
NM_000142.4(FGFR3):c.2135G>A (p.Arg712His) rs104886024
NM_000142.4(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190
NM_000142.4(FGFR3):c.2152A>G (p.Asn718Asp) rs587778358
NM_000142.4(FGFR3):c.299C>G (p.Ser100Cys) rs587778352
NM_000142.4(FGFR3):c.599G>T (p.Arg200Leu) rs587778353
NM_000142.4(FGFR3):c.62C>A (p.Ser21Tyr) rs587778351
NM_000142.4(FGFR3):c.749C>G (p.Pro250Arg) rs4647924
NM_000142.4(FGFR3):c.768G>T (p.Gln256His) rs587778354

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