Related gene-specific medical variations for Gene (Select 114804) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155125	NM_052916.3(RNF157):c.1802C>T (p.Thr601Met)	RNF157, RNF157-AS1 (T579M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2553234	NM_052916.3(RNF157):c.1773T>A (p.Asp591Glu)	RNF157, RNF157-AS1 (D569E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2532669	NM_052916.3(RNF157):c.2006C>T (p.Thr669Met)	RNF157, RNF157-AS1 (T647M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479746	NM_052916.3(RNF157):c.532G>A (p.Val178Met)	LOC126862647, RNF157 (V178M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476337	NM_052916.3(RNF157):c.473C>T (p.Ser158Leu)	LOC126862647, RNF157 (S158L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472321	NM_052916.3(RNF157):c.1946C>T (p.Ala649Val)	RNF157, RNF157-AS1 (A649V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2358922	NM_052916.3(RNF157):c.1913G>A (p.Cys638Tyr)	RNF157, RNF157-AS1 (C638Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339176	NM_052916.3(RNF157):c.388G>A (p.Val130Ile)	LOC126862647, RNF157 (V130I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302501	NM_052916.3(RNF157):c.2000C>G (p.Ser667Cys)	RNF157, RNF157-AS1 (S645C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207836	NM_052916.3(RNF157):c.457G>C (p.Asp153His)	LOC126862647, RNF157 (D153H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791204	NM_052916.3(RNF157):c.315G>A (p.Lys105=)	LOC126862647, RNF157	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 790187	NM_052916.3(RNF157):c.1821G>T (p.Thr607=)	RNF157, RNF157-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign