ClinVar Miner

List of variants in gene FGFR2 reported as likely benign by Invitae

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Total variants: 150
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.759T>G (p.Pro253=) rs3135755 0.00057
NM_000141.5(FGFR2):c.34G>A (p.Val12Met) rs143978938 0.00043
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=) rs149008039 0.00026
NM_000141.5(FGFR2):c.263T>C (p.Ile88Thr) rs200369248 0.00022
NM_000141.5(FGFR2):c.109+17C>G rs200633640 0.00018
NM_000141.5(FGFR2):c.501T>C (p.His167=) rs766869457 0.00014
NM_000141.5(FGFR2):c.568C>T (p.Arg190Trp) rs147987917 0.00013
NM_000141.5(FGFR2):c.1361C>T (p.Thr454Met) rs148672240 0.00012
NM_000141.5(FGFR2):c.748+18C>T rs377269009 0.00012
NM_000141.5(FGFR2):c.2426T>C (p.Leu809Pro) rs368003279 0.00011
NM_000141.5(FGFR2):c.289G>A (p.Ala97Thr) rs372430349 0.00011
NM_000141.5(FGFR2):c.625-10A>G rs201512833 0.00011
NM_000141.5(FGFR2):c.454+15G>A rs200275522 0.00010
NM_000141.5(FGFR2):c.182G>A (p.Arg61His) rs199575491 0.00007
NM_000141.5(FGFR2):c.2124C>T (p.Pro708=) rs140813163 0.00007
NM_000141.5(FGFR2):c.1362G>A (p.Thr454=) rs200183009 0.00006
NM_000141.5(FGFR2):c.1987-5T>G rs778413728 0.00006
NM_000141.5(FGFR2):c.201C>T (p.Ala67=) rs200386134 0.00006
NM_000141.5(FGFR2):c.420G>A (p.Ala140=) rs765024365 0.00006
NM_000141.5(FGFR2):c.748+19G>A rs372837794 0.00006
NM_000141.5(FGFR2):c.306C>T (p.Ser102=) rs368662264 0.00005
NM_000141.5(FGFR2):c.780C>T (p.Ala260=) rs778288494 0.00005
NM_000141.5(FGFR2):c.1302C>T (p.Ser434=) rs141297318 0.00004
NM_000141.5(FGFR2):c.1561+7G>A rs757328995 0.00004
NM_000141.5(FGFR2):c.2028T>C (p.Phe676=) rs766703071 0.00004
NM_000141.5(FGFR2):c.729G>A (p.Thr243=) rs199890227 0.00004
NM_000141.5(FGFR2):c.924C>T (p.Tyr308=) rs775459922 0.00004
NM_000141.5(FGFR2):c.1086G>A (p.Ala362=) rs151250769 0.00003
NM_000141.5(FGFR2):c.1440-14A>G rs1053077541 0.00003
NM_000141.5(FGFR2):c.1545C>T (p.Ala515=) rs778789088 0.00003
NM_000141.5(FGFR2):c.1818C>T (p.Cys606=) rs371395564 0.00003
NM_000141.5(FGFR2):c.2195+7G>A rs377397478 0.00003
NM_000141.5(FGFR2):c.2247G>A (p.Thr749=) rs1246437941 0.00003
NM_000141.5(FGFR2):c.2040C>T (p.Tyr680=) rs751495618 0.00002
NM_000141.5(FGFR2):c.2106G>A (p.Ser702=) rs794727163 0.00002
NM_000141.5(FGFR2):c.756G>A (p.Ser252=) rs138769323 0.00002
NM_000141.5(FGFR2):c.940-9G>A rs752752282 0.00002
NM_000141.5(FGFR2):c.1152G>A (p.Gly384=) rs772014466 0.00001
NM_000141.5(FGFR2):c.1155C>G (p.Val385=) rs531426519 0.00001
NM_000141.5(FGFR2):c.1239G>A (p.Pro413=) rs147674677 0.00001
NM_000141.5(FGFR2):c.1335G>T (p.Val445=) rs1460282965 0.00001
NM_000141.5(FGFR2):c.138A>C (p.Gln46His) rs748117555 0.00001
NM_000141.5(FGFR2):c.150C>T (p.Tyr50=) rs376622125 0.00001
NM_000141.5(FGFR2):c.1866T>C (p.Cys622=) rs369637667 0.00001
NM_000141.5(FGFR2):c.234C>T (p.His78=) rs778093907 0.00001
NM_000141.5(FGFR2):c.2448C>T (p.Asn816=) rs774232306 0.00001
NM_000141.5(FGFR2):c.252G>A (p.Arg84=) rs779848635 0.00001
NM_000141.5(FGFR2):c.377-6A>T rs1447764550 0.00001
NM_000141.5(FGFR2):c.390C>T (p.Ser130=) rs1029635273 0.00001
NM_000141.5(FGFR2):c.1002T>C (p.Phe334=)
NM_000141.5(FGFR2):c.1023G>A (p.Thr341=)
NM_000141.5(FGFR2):c.1023G>T (p.Thr341=) rs201648220
NM_000141.5(FGFR2):c.1084+20T>C rs1554928776
NM_000141.5(FGFR2):c.1084+8C>T rs1589827584
NM_000141.5(FGFR2):c.1085-13A>G
NM_000141.5(FGFR2):c.1085-15T>C
NM_000141.5(FGFR2):c.1085-8C>T
NM_000141.5(FGFR2):c.1085-9G>A
NM_000141.5(FGFR2):c.1086G>C (p.Ala362=) rs151250769
NM_000141.5(FGFR2):c.109+14T>C
NM_000141.5(FGFR2):c.109+4561_109+4562delinsCA rs2135437452
NM_000141.5(FGFR2):c.1095A>G (p.Arg365=)
NM_000141.5(FGFR2):c.110-22TC[3] rs773932794
NM_000141.5(FGFR2):c.114A>T (p.Pro38=) rs370046872
NM_000141.5(FGFR2):c.1164C>T (p.Ile388=)
NM_000141.5(FGFR2):c.1179A>G (p.Val393=)
NM_000141.5(FGFR2):c.1191G>A (p.Leu397=)
NM_000141.5(FGFR2):c.1242T>C (p.Ala414=)
NM_000141.5(FGFR2):c.1254G>T (p.Leu418=)
NM_000141.5(FGFR2):c.1287+11A>G rs758846086
NM_000141.5(FGFR2):c.1288-15G>A
NM_000141.5(FGFR2):c.1288-16_1288-15insTTG rs778424804
NM_000141.5(FGFR2):c.1288-8G>A
NM_000141.5(FGFR2):c.1326C>T (p.Thr442=)
NM_000141.5(FGFR2):c.1356T>A (p.Ser452=) rs2134060289
NM_000141.5(FGFR2):c.138A>G (p.Gln46=)
NM_000141.5(FGFR2):c.1392C>T (p.Ser464=)
NM_000141.5(FGFR2):c.141A>G (p.Pro47=)
NM_000141.5(FGFR2):c.1440-6A>G rs2134013964
NM_000141.5(FGFR2):c.1455G>A (p.Lys485=)
NM_000141.5(FGFR2):c.1485G>A (p.Val495=) rs1362401352
NM_000141.5(FGFR2):c.1536C>T (p.Val512=)
NM_000141.5(FGFR2):c.1561+10G>C rs758605716
NM_000141.5(FGFR2):c.1561+14C>T
NM_000141.5(FGFR2):c.1562-6del
NM_000141.5(FGFR2):c.159G>T (p.Ala53=) rs1047102
NM_000141.5(FGFR2):c.1672+20G>A
NM_000141.5(FGFR2):c.1673-8C>T
NM_000141.5(FGFR2):c.168G>A (p.Glu56=)
NM_000141.5(FGFR2):c.1695G>A (p.Glu565=)
NM_000141.5(FGFR2):c.1716C>T (p.Leu572=)
NM_000141.5(FGFR2):c.1746C>T (p.Pro582=) rs369850306
NM_000141.5(FGFR2):c.1830G>A (p.Leu610=) rs2133934402
NM_000141.5(FGFR2):c.1863+13C>T
NM_000141.5(FGFR2):c.1863+14A>G
NM_000141.5(FGFR2):c.1863+19A>G rs1164060462
NM_000141.5(FGFR2):c.1864-6T>C rs767324356
NM_000141.5(FGFR2):c.186C>T (p.Cys62=)
NM_000141.5(FGFR2):c.1986+8G>A
NM_000141.5(FGFR2):c.1987-20A>T rs772633227
NM_000141.5(FGFR2):c.2016A>T (p.Pro672=)
NM_000141.5(FGFR2):c.2057+17T>A
NM_000141.5(FGFR2):c.2091C>T (p.Phe697=)
NM_000141.5(FGFR2):c.2196-11A>G
NM_000141.5(FGFR2):c.2196-19G>A
NM_000141.5(FGFR2):c.2196-5C>T
NM_000141.5(FGFR2):c.2223T>C (p.His741=)
NM_000141.5(FGFR2):c.222G>A (p.Lys74=)
NM_000141.5(FGFR2):c.2256G>A (p.Gln752=)
NM_000141.5(FGFR2):c.2302-15C>T
NM_000141.5(FGFR2):c.2302-17C>T
NM_000141.5(FGFR2):c.2340A>G (p.Ser780=)
NM_000141.5(FGFR2):c.2421A>G (p.Pro807=)
NM_000141.5(FGFR2):c.2424C>T (p.Cys808=) rs759496942
NM_000141.5(FGFR2):c.27C>T (p.Cys9=)
NM_000141.5(FGFR2):c.288C>T (p.Gly96=)
NM_000141.5(FGFR2):c.291C>A (p.Ala97=) rs2135114699
NM_000141.5(FGFR2):c.376+15C>T
NM_000141.5(FGFR2):c.376+20C>A
NM_000141.5(FGFR2):c.390C>G (p.Ser130=) rs1029635273
NM_000141.5(FGFR2):c.454+20C>T
NM_000141.5(FGFR2):c.455-20_455-15del rs754925091
NM_000141.5(FGFR2):c.455-9C>T
NM_000141.5(FGFR2):c.543C>T (p.Ala181=) rs150598483
NM_000141.5(FGFR2):c.591G>A (p.Glu197=)
NM_000141.5(FGFR2):c.625-8C>A rs1853240523
NM_000141.5(FGFR2):c.657A>G (p.Glu219=)
NM_000141.5(FGFR2):c.696A>T (p.Val232=)
NM_000141.5(FGFR2):c.711C>T (p.Tyr237=)
NM_000141.5(FGFR2):c.714G>A (p.Gly238=) rs1276387170
NM_000141.5(FGFR2):c.720C>T (p.Ile240=)
NM_000141.5(FGFR2):c.748+10C>T
NM_000141.5(FGFR2):c.748+14T>A
NM_000141.5(FGFR2):c.748+15C>T
NM_000141.5(FGFR2):c.748+7T>C
NM_000141.5(FGFR2):c.749-11C>G rs2134320757
NM_000141.5(FGFR2):c.749-12TC[2] rs760498153
NM_000141.5(FGFR2):c.749-19dup
NM_000141.5(FGFR2):c.807G>A (p.Val269=) rs2134316233
NM_000141.5(FGFR2):c.810C>T (p.Val270=)
NM_000141.5(FGFR2):c.837G>A (p.Lys279=)
NM_000141.5(FGFR2):c.840T>G (p.Val280=)
NM_000141.5(FGFR2):c.903C>T (p.Tyr301=)
NM_000141.5(FGFR2):c.939+11T>A
NM_000141.5(FGFR2):c.940-4C>G
NM_000141.5(FGFR2):c.945C>T (p.Ala315=)
NM_000141.5(FGFR2):c.96A>G (p.Thr32=)
NM_000141.5(FGFR2):c.984T>C (p.Tyr328=)
NM_000141.5(FGFR2):c.990G>T (p.Arg330=)
NM_000141.5(FGFR2):c.996A>G (p.Val332=) rs1420060403

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