ClinVar for Gene (Select 100130348) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179378	NM_001282448.2(TMEM262):c.282C>T (p.Asn94=)	TMEM262 (R84W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2513145	NM_001282448.2(TMEM262):c.108C>G (p.Asp36Glu)	TMEM262 (D36E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370236	NM_001282448.2(TMEM262):c.59C>T (p.Thr20Met)	TMEM262 (T20M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2293084	NM_001282448.2(TMEM262):c.106G>A (p.Asp36Asn)	TMEM262 (D36N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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