"Ambry Genetics"[submitter] AND "TEX46"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176413	NM_001242521.2(TEX46):c.201G>A (p.Met67Ile)	LOC126805656, TEX46 (M67I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176412	NM_001242521.2(TEX46):c.181C>T (p.Arg61Trp)	LOC126805656, TEX46 (R61W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176414	NM_001242521.2(TEX46):c.35C>T (p.Thr12Ile)	TEX46 (T12I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar