"Ambry Genetics"[submitter] AND "TATDN3"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255350	NM_001042552.3(TATDN3):c.14G>A (p.Gly5Asp)	LOC129932483, TATDN3 (G5D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608620	NM_001042552.3(TATDN3):c.185T>C (p.Phe62Ser)	TATDN3 (F62S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308813	NM_001042552.3(TATDN3):c.241A>G (p.Arg81Gly)	TATDN3 (R81G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608377	NM_001042552.3(TATDN3):c.275T>C (p.Leu92Ser)	TATDN3 (L92S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219417	NM_001042552.3(TATDN3):c.313A>G (p.Ile105Val)	TATDN3 (I105V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366180	NM_001042552.3(TATDN3):c.436G>A (p.Val146Met)	TATDN3 (V125M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272203	NM_001042552.3(TATDN3):c.445C>T (p.Arg149Cys)	TATDN3 (R149C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550690	NM_001042552.3(TATDN3):c.466A>G (p.Ile156Val)	TATDN3 (I135V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3174327	NM_001042552.3(TATDN3):c.481G>C (p.Glu161Gln)	TATDN3 (E140Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328312	NM_001042552.3(TATDN3):c.503T>C (p.Leu168Pro)	TATDN3 (L168P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324548	NM_001042552.3(TATDN3):c.524G>A (p.Arg175Gln)	TATDN3 (R154Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238169	NM_001042552.3(TATDN3):c.545G>A (p.Gly182Glu)	TATDN3 (G161E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349159	NM_001042552.3(TATDN3):c.806G>A (p.Arg269Gln)	TATDN3 (R248Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign