List of variants in gene F10 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000504.4(F10):c.424G>A (p.Glu142Lys)	rs61753266	0.00347
NM_000504.4(F10):c.1012G>A (p.Val338Met)	rs121964947	0.00001
NM_000504.4(F10):c.1073C>T (p.Thr358Met)	rs768222784	0.00001
NM_000504.4(F10):c.140A>G (p.Glu47Gly)	rs121964943	0.00001
NM_000504.4(F10):c.161A>G (p.Glu54Gly)	rs121964944	0.00001
NM_000504.4(F10):c.1096C>T (p.Arg366Cys)	rs104894392
NM_000504.4(F10):c.1120T>C (p.Ser374Pro)	rs121964941
NM_000504.4(F10):c.160G>A (p.Glu54Lys)	rs121964939
NM_000504.4(F10):c.214G>C (p.Glu72Gln)	rs121964945
NM_000504.4(F10):c.61G>A (p.Gly21Arg)	rs753790195
NM_000504.4(F10):c.814del (p.Ile271_Leu272insTer)	rs387906506
NM_000504.4(F10):c.859A>T (p.Arg287Trp)	rs121964948
NM_000504.4(F10):c.964G>A (p.Asp322Asn)	rs121964942
NM_001312675.2(F10):c.*138C>T	rs121964940
NM_001312675.2(F10):c.855+10G>C	rs121964946

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