List of variants in gene FRAS1 reported as uncertain significance by Eurofins NTD LLC (GA)

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.4579C>T (p.Arg1527Trp)	rs1872267	0.00253
NM_025074.7(FRAS1):c.7033G>A (p.Glu2345Lys)	rs56291926	0.00241
NM_025074.7(FRAS1):c.7029+7G>A	rs183687186	0.00159
NM_025074.7(FRAS1):c.11264C>T (p.Pro3755Leu)	rs199510509	0.00133
NM_025074.7(FRAS1):c.7039G>T (p.Val2347Phe)	rs201369510	0.00131
NM_025074.7(FRAS1):c.108+10T>G	rs76831011	0.00115
NM_025074.7(FRAS1):c.641C>T (p.Pro214Leu)	rs200053639	0.00108
NM_025074.7(FRAS1):c.3058C>T (p.Arg1020Cys)	rs200292361	0.00099
NM_025074.7(FRAS1):c.969G>A (p.Val323=)	rs377333036	0.00063
NM_025074.7(FRAS1):c.11306A>G (p.Asn3769Ser)	rs112039037	0.00053
NM_025074.7(FRAS1):c.3010+9G>A	rs148841455	0.00051
NM_025074.7(FRAS1):c.9364C>T (p.Arg3122Trp)	rs200346497	0.00046
NM_025074.7(FRAS1):c.4364C>T (p.Ala1455Val)	rs201693179	0.00045
NM_025074.7(FRAS1):c.9627C>T (p.Tyr3209=)	rs377369857	0.00036
NM_025074.7(FRAS1):c.217-3C>T	rs150498567	0.00025
NM_025074.7(FRAS1):c.990A>G (p.Glu330=)	rs374045395	0.00017
NM_025074.7(FRAS1):c.10128C>T (p.His3376=)	rs369331788	0.00013
NM_025074.7(FRAS1):c.11317G>C (p.Val3773Leu)	rs150567662	0.00013
NM_025074.7(FRAS1):c.11683G>A (p.Val3895Ile)	rs370511192	0.00013
NM_025074.7(FRAS1):c.9375T>A (p.His3125Gln)	rs370907958	0.00013
NM_025074.7(FRAS1):c.2862G>A (p.Thr954=)	rs144065807	0.00012
NM_025074.7(FRAS1):c.237T>C (p.Ala79=)	rs370345916	0.00010
NM_025074.7(FRAS1):c.4729A>T (p.Thr1577Ser)	rs183594682	0.00010
NM_025074.7(FRAS1):c.6473A>C (p.Glu2158Ala)	rs794727681	0.00009
NM_025074.7(FRAS1):c.1503C>T (p.Asp501=)	rs370655417	0.00008
NM_025074.7(FRAS1):c.2803G>C (p.Gly935Arg)	rs200113218	0.00006
NM_025074.7(FRAS1):c.39G>A (p.Ala13=)	rs773457837	0.00006
NM_025074.7(FRAS1):c.808C>T (p.Arg270Cys)	rs773283272	0.00005
NM_025074.7(FRAS1):c.9315C>T (p.Pro3105=)	rs772629108	0.00004
NM_025074.7(FRAS1):c.9450G>T (p.Val3150=)	rs372168929	0.00004
NM_025074.7(FRAS1):c.4291G>A (p.Asp1431Asn)	rs371136161	0.00003
NM_025074.7(FRAS1):c.8752+9T>C	rs191984935	0.00003
NM_025074.7(FRAS1):c.8827C>T (p.Arg2943Trp)	rs751338045	0.00003
NM_025074.7(FRAS1):c.3786T>A (p.His1262Gln)	rs372363321	0.00002
NM_025074.7(FRAS1):c.11634G>C (p.Lys3878Asn)	rs749106181	0.00001
NM_025074.7(FRAS1):c.1897C>T (p.Arg633Cys)	rs370349229	0.00001
NM_025074.7(FRAS1):c.3523G>A (p.Glu1175Lys)	rs746130442	0.00001
NM_025074.7(FRAS1):c.6876T>C (p.Asp2292=)	rs779794904	0.00001
NM_025074.7(FRAS1):c.11219C>A (p.Thr3740Lys)	rs757591237
NM_025074.7(FRAS1):c.3885T>A (p.Gly1295=)	rs1553953731
NM_025074.7(FRAS1):c.4365G>C (p.Ala1455=)	rs375417798
NM_025074.7(FRAS1):c.4857A>G (p.Val1619=)	rs886044144
NM_025074.7(FRAS1):c.5205C>A (p.His1735Gln)	rs533608491
NM_025074.7(FRAS1):c.6698C>T (p.Thr2233Ile)	rs794727686
NM_025074.7(FRAS1):c.71C>A (p.Ser24Tyr)	rs794726952
NM_025074.7(FRAS1):c.7632C>T (p.Ser2544=)	rs886043689
NM_025074.7(FRAS1):c.8846A>T (p.Tyr2949Phe)	rs200212920
NM_025074.7(FRAS1):c.9123C>T (p.Thr3041=)	rs763383473

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