ClinVar Miner

List of variants in gene FGFR3 reported as benign by Invitae

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Total variants: 37
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HGVS dbSNP
NM_000142.4(FGFR3):c.1023G>A (p.Ala341=) rs147833498
NM_000142.4(FGFR3):c.1075+5C>T rs3135885
NM_000142.4(FGFR3):c.1535-8G>T rs111460786
NM_000142.4(FGFR3):c.1668G>A (p.Glu556=) rs1388294342
NM_000142.4(FGFR3):c.1719G>A (p.Pro573=) rs772157613
NM_000142.4(FGFR3):c.1959+8C>T rs371666188
NM_000142.4(FGFR3):c.2169-5C>T
NM_000142.4(FGFR3):c.445+3A>G rs3135868
NM_000142.4(FGFR3):c.446-5C>T rs144211980
NM_000142.4(FGFR3):c.615+6C>A rs2305182
NM_000142.4(FGFR3):c.615+8C>G rs17878375
NM_000142.4(FGFR3):c.713G>A (p.Arg238Gln) rs199944818
NM_000142.4(FGFR3):c.930+10C>T rs534857289
NM_000142.4(FGFR3):c.933G>A (p.Thr311=) rs142805104
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302
NM_000142.5(FGFR3):c.252G>A (p.Ser84=) rs367973461
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179
NM_000142.5(FGFR3):c.393G>A (p.Ser131=) rs55662109
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180
NM_000142.5(FGFR3):c.654G>C (p.Val218=) rs147769045
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370
NM_000142.5(FGFR3):c.678C>T (p.Tyr226=) rs141575580
NM_000142.5(FGFR3):c.771G>A (p.Ala257=) rs138334098
NM_000142.5(FGFR3):c.990C>T (p.Thr330=) rs2305185

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