"Ambry Genetics"[submitter] AND "TAMM41"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2248379	NM_001284401.2(TAMM41):c.982A>C (p.Met328Leu)	TAMM41 (M307L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234350	NM_001284401.2(TAMM41):c.970A>G (p.Lys324Glu)	TAMM41 (K303E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173700	NM_001284401.2(TAMM41):c.948G>T (p.Lys316Asn)	TAMM41 (K275N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173699	NM_001284401.2(TAMM41):c.845A>G (p.Asp282Gly)	TAMM41 (D116G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258161	NM_001284401.2(TAMM41):c.817G>A (p.Glu273Lys)	TAMM41 (E273K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402439	NM_001284401.2(TAMM41):c.814G>T (p.Val272Leu)	TAMM41 (V106L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409408	NM_001284401.2(TAMM41):c.709A>G (p.Ile237Val)	TAMM41 (I237V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292644	NM_001284401.2(TAMM41):c.638G>A (p.Arg213Gln)	TAMM41 (R172Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173698	NM_001284401.2(TAMM41):c.596C>A (p.Thr199Lys)	TAMM41 (T199K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173697	NM_001284401.2(TAMM41):c.536T>C (p.Ile179Thr)	TAMM41 (I138T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173696	NM_001284401.2(TAMM41):c.508G>A (p.Glu170Lys)	TAMM41 (E4K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345672	NM_001284401.2(TAMM41):c.479C>T (p.Ala160Val)	TAMM41 (A160V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3173695	NM_001284401.2(TAMM41):c.450A>T (p.Arg150Ser)	TAMM41 (R150S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3173694	NM_001284401.2(TAMM41):c.445C>G (p.Leu149Val)	TAMM41 (L149V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3324332	NM_001284401.2(TAMM41):c.398G>A (p.Arg133Gln)	TAMM41 (R133Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2258947	NM_001284401.2(TAMM41):c.398G>T (p.Arg133Leu)	TAMM41 (R133L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3173693	NM_001284401.2(TAMM41):c.301A>G (p.Ile101Val)	TAMM41 (I60V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2530113	NM_001284401.2(TAMM41):c.259A>G (p.Ile87Val)	TAMM41 (I87V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3324334	NM_001284401.2(TAMM41):c.254C>T (p.Thr85Met)	TAMM41 (T85M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3324333	NM_001284401.2(TAMM41):c.233T>C (p.Val78Ala)	TAMM41 (V37A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2462332	NM_001284401.2(TAMM41):c.224T>C (p.Phe75Ser)	TAMM41 (F34S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2225349	NM_001284401.2(TAMM41):c.172C>G (p.Pro58Ala)	TAMM41 (P17A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 22