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

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3175397	NM_003211.6(TDG):c.7G>C (p.Ala3Pro)	TDG (A3P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3175391	NM_003211.6(TDG):c.10G>A (p.Glu4Lys)	TDG (E4K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2378166	NM_003211.6(TDG):c.17C>G (p.Ala6Gly)	TDG (A6G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3175396	NM_003211.6(TDG):c.53A>G (p.Tyr18Cys)	TDG (Y18C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175399	NM_003211.6(TDG):c.86C>G (p.Ala29Gly)	TDG (A29G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175393	NM_003211.6(TDG):c.128A>T (p.Glu43Val)	TDG (E43V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175394	NM_003211.6(TDG):c.129A>T (p.Glu43Asp)	TDG (E43D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296811	NM_003211.6(TDG):c.140C>G (p.Pro47Arg)	TDG (P47R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175395	NM_003211.6(TDG):c.295A>C (p.Thr99Pro)	TDG (T99P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2484598	NM_003211.6(TDG):c.352G>A (p.Glu118Lys)	TDG (E118K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2471846	NM_003211.6(TDG):c.534T>A (p.Asp178Glu)	TDG (D178E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475474	NM_003211.6(TDG):c.574A>G (p.Met192Val)	TDG (M192V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245477	NM_003211.6(TDG):c.733G>A (p.Val245Ile)	TDG (V102I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175398	NM_003211.6(TDG):c.868A>C (p.Ile290Leu)	TDG (I147L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554930	NM_003211.6(TDG):c.868A>G (p.Ile290Val)	TDG (I290V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601204	NM_003211.6(TDG):c.911G>A (p.Arg304Gln)	TDG (R161Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175400	NM_003211.6(TDG):c.985G>A (p.Val329Ile)	TDG (V186I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325080	NM_003211.6(TDG):c.1136C>G (p.Pro379Arg)	TDG (P379R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance