ClinVar Miner

List of variants in gene FGFR3 reported as likely benign by Invitae

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Gene type:
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Total variants: 55
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HGVS dbSNP
NM_000142.4(FGFR3):c.1146C>T (p.Gly382=) rs762689187
NM_000142.4(FGFR3):c.1267-8C>T rs1553847171
NM_000142.4(FGFR3):c.1320C>T (p.Ile440=) rs190111780
NM_000142.4(FGFR3):c.1356C>A (p.Ala452=) rs149555011
NM_000142.4(FGFR3):c.1404T>G (p.Ser468=) rs1391284081
NM_000142.4(FGFR3):c.1431C>T (p.Pro477=) rs1351116736
NM_000142.4(FGFR3):c.1476C>T (p.Ile492=) rs373254179
NM_000142.4(FGFR3):c.1513G>A (p.Val505Ile) rs144546453
NM_000142.4(FGFR3):c.154G>A (p.Gly52Ser) rs140087676
NM_000142.4(FGFR3):c.1551G>A (p.Lys517=) rs142622642
NM_000142.4(FGFR3):c.159C>T (p.Ser53=) rs143548893
NM_000142.4(FGFR3):c.1644C>T (p.Gly548=) rs756321317
NM_000142.4(FGFR3):c.1645+8C>T rs372987620
NM_000142.4(FGFR3):c.1645+9G>A rs376263017
NM_000142.4(FGFR3):c.1671C>T (p.Tyr557=) rs370408732
NM_000142.4(FGFR3):c.1706C>T (p.Ala569Val) rs146672976
NM_000142.4(FGFR3):c.1764G>A (p.Gln588=) rs765360194
NM_000142.4(FGFR3):c.1845C>T (p.His615=) rs375856533
NM_000142.4(FGFR3):c.1878C>T (p.Thr626=) rs369137031
NM_000142.4(FGFR3):c.1899C>T (p.Ile633=) rs748492424
NM_000142.4(FGFR3):c.192C>T (p.Pro64=) rs766462409
NM_000142.4(FGFR3):c.1960-7C>T rs779177992
NM_000142.4(FGFR3):c.1971C>T (p.Pro657=) rs922106076
NM_000142.4(FGFR3):c.2082G>A (p.Pro694=) rs765659195
NM_000142.4(FGFR3):c.2265G>A (p.Thr755=) rs755791719
NM_000142.4(FGFR3):c.2275-3C>T rs770863154
NM_000142.4(FGFR3):c.2316G>A (p.Pro772=) rs200629304
NM_000142.4(FGFR3):c.2331C>T (p.Thr777=) rs189264142
NM_000142.4(FGFR3):c.2412G>A (p.Ser804=) rs375563964
NM_000142.4(FGFR3):c.2418G>A (p.Thr806=) rs779088139
NM_000142.4(FGFR3):c.304G>A (p.Glu102Lys) rs558935109
NM_000142.4(FGFR3):c.513C>T (p.Thr171=) rs373209526
NM_000142.4(FGFR3):c.616-6G>A rs17883400
NM_000142.4(FGFR3):c.660C>A (p.Pro220=) rs146927248
NM_000142.4(FGFR3):c.669C>T (p.Arg223=) rs749024125
NM_000142.4(FGFR3):c.726G>C (p.Thr242=) rs1399793508
NM_000142.4(FGFR3):c.740-9C>T rs886038257
NM_000142.4(FGFR3):c.775C>T (p.Leu259=) rs765971064
NM_000142.4(FGFR3):c.879G>C (p.Val293=) rs757808716
NM_000142.4(FGFR3):c.921C>G (p.Thr307=) rs148518372
NM_000142.4(FGFR3):c.963A>G (p.Leu321=) rs201221388
NM_000142.5(FGFR3):c.1371C>T (p.Leu457=) rs199758988
NM_000142.5(FGFR3):c.150C>T (p.Val50=) rs750641928
NM_000142.5(FGFR3):c.1550A>G (p.Lys517Arg) rs139707740
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064
NM_000142.5(FGFR3):c.1752G>A (p.Pro584=) rs139020690
NM_000142.5(FGFR3):c.1953= (p.Thr651=) rs7688609
NM_000142.5(FGFR3):c.201T>C (p.Gly67=) rs752621056
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190
NM_000142.5(FGFR3):c.2259C>T (p.Thr753=) rs146662137
NM_000142.5(FGFR3):c.312C>T (p.Ser104=) rs377018654
NM_000142.5(FGFR3):c.573C>T (p.Asn191=) rs377492283
NM_000142.5(FGFR3):c.807C>T (p.Ser269=) rs199614237
NM_001163213.1(FGFR3):c.2036+9C>T rs373627757
NM_001163213.1(FGFR3):c.616-8C>T rs372304346

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