"Ambry Genetics"[submitter] AND "MSMP"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296451	NM_001044264.3(MSMP):c.353G>C (p.Gly118Ala)	LOC126860622, MSMP +1 more (G118A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3212018	NM_001044264.3(MSMP):c.332G>A (p.Arg111Gln)	LOC126860622, MSMP +1 more (R111Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3212014	NM_001044264.3(MSMP):c.281G>A (p.Arg94His)	LOC126860622, MSMP +1 more (R94H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3212010	NM_001044264.3(MSMP):c.263C>T (p.Pro88Leu)	LOC126860622, MSMP +1 more (P88L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3296450	NM_001044264.3(MSMP):c.104A>G (p.Tyr35Cys)	LOC126860622, MSMP +1 more (Y35C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3296449	NM_001044264.3(MSMP):c.65G>T (p.Cys22Phe)	LOC126860622, MSMP +1 more (C22F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3212023	NM_001044264.3(MSMP):c.49G>T (p.Gly17Cys)	LOC126860622, MSMP +1 more (G17C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458725	NM_001044264.3(MSMP):c.4G>A (p.Ala2Thr)	RGP1, MSMP (A2T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance