"Genome-Nilou Lab"[submitter] AND "SLFN14"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1245977	NM_001129820.2(SLFN14):c.2735A>T (p.Tyr912Phe)	SLFN14 (Y912F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1239057	NM_001129820.2(SLFN14):c.2713C>T (p.Leu905Phe)	SLFN14 (L905F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1333128	NM_001129820.2(SLFN14):c.1348A>G (p.Lys450Glu)	LOC107985033, SLFN14 (K450E)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign
Select item 1244326	NM_001129820.2(SLFN14):c.1153A>G (p.Lys385Glu)	LOC107985033, SLFN14 (K385E)	Single nucleotide variant (non-coding transcript variant +1 more)	Platelet-type bleeding disorder 20 +1 more	GBenign
Select item 1246755	NM_001129820.2(SLFN14):c.1066C>T (p.Pro356Ser)	LOC107985033, SLFN14 (P356S)	Single nucleotide variant (non-coding transcript variant +1 more)	Platelet-type bleeding disorder 20 +1 more	GBenign
Select item 1286606	NM_001129820.2(SLFN14):c.1061-11T>C	LOC107985033, SLFN14	Single nucleotide variant (non-coding transcript variant +1 more)	Platelet-type bleeding disorder 20 +1 more	GBenign
Select item 1333129	NM_001129820.2(SLFN14):c.278A>G (p.Gln93Arg)	SLFN14 (Q93R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign

ClinVar