"PreventionGenetics, part of Exact Sciences"[submitter] AND "FYB1"[gen - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038884	NM_001465.6(FYB1):c.2412C>T (p.Val804=)	FYB1	Single nucleotide variant (synonymous variant)	FYB1-related disorder	GLikely benign
Select item 3043812	NM_001465.6(FYB1):c.2000G>A (p.Arg667Gln)	FYB1 (R667Q +1 more)	Single nucleotide variant (missense variant +1 more)	FYB1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2655441	NM_001465.6(FYB1):c.1941G>A (p.Thr647=)	FYB1	Single nucleotide variant (synonymous variant +1 more)	FYB1-related disorder +1 more	GLikely benign
Select item 3054911	NM_001465.6(FYB1):c.1906G>T (p.Gly636Cys)	FYB1 (G636C +1 more)	Single nucleotide variant (missense variant)	FYB1-related disorder	GLikely benign
Select item 3039741	NM_001465.6(FYB1):c.1516-5T>C	FYB1	Single nucleotide variant (intron variant)	FYB1-related disorder	GLikely benign
Select item 3057548	NM_001465.6(FYB1):c.1281G>A (p.Pro427=)	FYB1	Single nucleotide variant (synonymous variant)	FYB1-related disorder	GLikely benign
Select item 3038317	NM_001465.6(FYB1):c.1280C>T (p.Pro427Leu)	FYB1 (P427L +1 more)	Single nucleotide variant (missense variant)	FYB1-related disorder	GLikely benign
Select item 3053173	NM_001465.6(FYB1):c.982C>A (p.Gln328Lys)	FYB1 (Q328K +1 more)	Single nucleotide variant (missense variant)	FYB1-related disorder	GBenign
Select item 3059425	NM_001465.6(FYB1):c.804G>A (p.Ala268=)	FYB1	Single nucleotide variant (synonymous variant)	FYB1-related disorder	GLikely benign
Select item 3042900	NM_001465.6(FYB1):c.606G>A (p.Pro202=)	FYB1	Single nucleotide variant (synonymous variant)	FYB1-related disorder	GLikely benign
Select item 3037434	NM_001465.6(FYB1):c.410C>T (p.Pro137Leu)	FYB1 (P137L +1 more)	Single nucleotide variant (missense variant)	FYB1-related disorder	GLikely benign
Select item 3033523	NM_001465.6(FYB1):c.290G>T (p.Ser97Ile)	FYB1 (S107I +1 more)	Single nucleotide variant (missense variant)	FYB1-related disorder	GLikely benign
Select item 2571222	NM_001465.6(FYB1):c.243G>A (p.Pro81=)	FYB1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3058681	NM_001465.6(FYB1):c.18G>A (p.Thr6=)	FYB1	Single nucleotide variant (synonymous variant)	FYB1-related disorder	GLikely benign