"Ambry Genetics"[submitter] AND "MRPS25"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380158	NM_022497.5(MRPS25):c.496G>A (p.Ala166Thr)	MRPS25 (A166T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2356439	NM_022497.5(MRPS25):c.244T>C (p.Ser82Pro)	MRPS25 (S82P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2261629	NM_022497.5(MRPS25):c.236A>G (p.Tyr79Cys)	MRPS25 (Y79C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2309479	NM_022497.5(MRPS25):c.128G>T (p.Gly43Val)	MRPS25 (G43V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2560121	NM_022497.5(MRPS25):c.121G>T (p.Gly41Cys)	MRPS25 (G41C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2243220	NM_022497.5(MRPS25):c.107C>A (p.Thr36Lys)	MRPS25 (T36K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2531992	NM_022497.5(MRPS25):c.64G>A (p.Val22Met)	MRPS25 (V22M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546932	NM_022497.5(MRPS25):c.56G>A (p.Gly19Glu)	MRPS25 (G19E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2342960	NM_022497.5(MRPS25):c.4C>T (p.Pro2Ser)	MRPS25 (P2S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance