"Ambry Genetics"[submitter] AND "LOC108660406"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2391601	NM_001377405.1(ATXN7):c.101A>C (p.Gln34Pro)	ATXN7, LOC108660406 +1 more (Q34P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334908	NM_001377405.1(ATXN7):c.111G>C (p.Gln37His)	ATXN7, LOC108660406 +1 more (Q37H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance