List of variants in gene FGFR1 reported as uncertain significance for integumentary system benign neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.899T>C (p.Ile300Thr)	rs121909633	0.00042
NM_023110.3(FGFR1):c.422C>G (p.Thr141Arg)	rs200482627	0.00014
NM_023110.3(FGFR1):c.231C>G (p.Asn77Lys)	rs767195580	0.00010
NM_023110.3(FGFR1):c.1520G>A (p.Arg507His)	rs369356672	0.00009
NM_023110.3(FGFR1):c.1408C>T (p.Arg470Cys)	rs781310679	0.00007
NM_023110.3(FGFR1):c.1186G>A (p.Val396Ile)	rs752627281	0.00006
NM_023110.3(FGFR1):c.2428C>T (p.His810Tyr)	rs759376422	0.00004
NM_023110.3(FGFR1):c.566G>A (p.Arg189His)	rs778166317	0.00004
NM_023110.3(FGFR1):c.937-14G>A	rs779223305	0.00004
NM_023110.3(FGFR1):c.1424G>A (p.Arg475Gln)	rs747333248	0.00003
NM_023110.3(FGFR1):c.1139A>G (p.Tyr380Cys)	rs777103792	0.00002
NM_023110.3(FGFR1):c.1342C>T (p.Arg448Trp)	rs749903780	0.00002
NM_023110.3(FGFR1):c.2267G>A (p.Arg756His)	rs374473310	0.00002
NM_023110.3(FGFR1):c.2426G>A (p.Arg809Gln)	rs771680156	0.00002
NM_023110.3(FGFR1):c.2465G>A (p.Arg822His)	rs758677681	0.00002
NM_023110.3(FGFR1):c.83C>T (p.Pro28Leu)	rs145434725	0.00002
NM_023110.3(FGFR1):c.*112C>T	rs1189535138	0.00001
NM_023110.3(FGFR1):c.1072G>A (p.Val358Ile)	rs774768179	0.00001
NM_023110.3(FGFR1):c.1114C>T (p.Pro372Ser)	rs377648976	0.00001
NM_023110.3(FGFR1):c.128T>G (p.Phe43Cys)	rs1085307493	0.00001
NM_023110.3(FGFR1):c.1333C>T (p.Arg445Trp)	rs781608303	0.00001
NM_023110.3(FGFR1):c.1447C>T (p.Pro483Ser)	rs397515444	0.00001
NM_023110.3(FGFR1):c.166C>T (p.Arg56Trp)	rs1034848904	0.00001
NM_023110.3(FGFR1):c.1711G>A (p.Glu571Lys)	rs771720144	0.00001
NM_023110.3(FGFR1):c.173G>A (p.Arg58Gln)	rs200116660	0.00001
NM_023110.3(FGFR1):c.20T>G (p.Leu7Arg)	rs532741632	0.00001
NM_023110.3(FGFR1):c.2200C>T (p.Arg734Trp)	rs1329256283	0.00001
NM_023110.3(FGFR1):c.2350C>T (p.Arg784Trp)	rs377149398	0.00001
NM_023110.3(FGFR1):c.2370_2371del (p.Glu792fs)	rs767698667	0.00001
NM_023110.3(FGFR1):c.332C>T (p.Thr111Ile)	rs775020833	0.00001
NM_023110.3(FGFR1):c.346G>A (p.Val116Ile)	rs747842199	0.00001
NM_023110.3(FGFR1):c.381T>G (p.Asp127Glu)	rs750795714	0.00001
NM_023110.3(FGFR1):c.442C>T (p.Arg148Cys)	rs780153672	0.00001
NM_023110.3(FGFR1):c.443G>A (p.Arg148His)	rs515726222	0.00001
NM_023110.3(FGFR1):c.584A>G (p.Lys195Arg)	rs770139002	0.00001
NM_023110.3(FGFR1):c.8G>A (p.Ser3Asn)	rs751651299	0.00001
NM_023110.3(FGFR1):c.-88-3566dup	rs1424371425
NM_023110.3(FGFR1):c.1495G>A (p.Gly499Arg)	rs759552236
NM_023110.3(FGFR1):c.1694C>T (p.Ser565Phe)	rs768223019
NM_023110.3(FGFR1):c.1727G>A (p.Arg576Gln)	rs1482868825
NM_023110.3(FGFR1):c.2251G>A (p.Val751Met)	rs2150520798
NM_023110.3(FGFR1):c.2323C>G (p.Gln775Glu)	rs1232665126
NM_023110.3(FGFR1):c.289G>T (p.Gly97Cys)	rs1260404537

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