"Daryl Scott Lab, Baylor College of Medicine"[submitter] AND "FRAS1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 369975	NM_025074.7(FRAS1):c.2389G>A (p.Glu797Lys)	FRAS1 (E797K)	Single nucleotide variant (missense variant)	FRAS1-related disorder	GUncertain significance
Select item 369978	NM_025074.7(FRAS1):c.6323A>T (p.Asp2108Val)	FRAS1 (D2108V)	Single nucleotide variant (missense variant)	Congenital diaphragmatic hernia	Grisk factor
Select item 198348	NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln)	FRAS1 (R3269Q)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign

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ClinVar