Related gene-specific medical variations for Gene (Select 100526831) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3451242	NM_001017390.3(SULT1A4):c.26G>A (p.Arg9His)	SLX1B-SULT1A4, SULT1A4 (R9H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3445757	NM_024044.5(SLX1B):c.811G>A (p.Asp271Asn)	SLX1B, SLX1B-SULT1A4 (D157N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320607	NM_024044.5(SLX1B):c.762C>G (p.Asp254Glu)	SLX1B, SLX1B-SULT1A4 (D140E +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3166187	NM_024044.5(SLX1B):c.743T>A (p.Ile248Asn)	SLX1B, SLX1B-SULT1A4 (I246N +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2646362	NM_001017390.3(SULT1A4):c.42C>T (p.Tyr14=)	SLX1B-SULT1A4, SULT1A4	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2603995	NM_024044.5(SLX1B):c.713G>T (p.Cys238Phe)	SLX1B, SLX1B-SULT1A4 (C236F +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2386455	NM_024044.5(SLX1B):c.607C>T (p.Pro203Ser)	SLX1B, SLX1B-SULT1A4 (P201S +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2233960	NM_024044.5(SLX1B):c.821A>G (p.Glu274Gly)	SLX1B, SLX1B-SULT1A4 (E160G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance