TTPAL[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330163	NM_001039199.3(TTPAL):c.7G>A (p.Glu3Lys)	TTPAL (E3K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184673	NM_001039199.3(TTPAL):c.86C>T (p.Pro29Leu)	TTPAL (P29L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330164	NM_001039199.3(TTPAL):c.131G>A (p.Arg44Gln)	TTPAL (R44Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184669	NM_001039199.3(TTPAL):c.196C>T (p.Arg66Trp)	TTPAL (R66W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526436	NM_001039199.3(TTPAL):c.281G>A (p.Arg94Gln)	TTPAL (R94Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184670	NM_001039199.3(TTPAL):c.321A>C (p.Arg107Ser)	TTPAL (R107S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184671	NM_001039199.3(TTPAL):c.385T>C (p.Phe129Leu)	TTPAL (F129L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609230	NM_001039199.3(TTPAL):c.412C>A (p.Pro138Thr)	TTPAL (P138T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596785	NM_001039199.3(TTPAL):c.430G>A (p.Val144Ile)	TTPAL (V144I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204243	NM_001039199.3(TTPAL):c.501G>T (p.Leu167Phe)	TTPAL (L167F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606497	NM_001039199.3(TTPAL):c.548T>C (p.Ile183Thr)	TTPAL (I183T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594009	NM_001039199.3(TTPAL):c.568A>G (p.Lys190Glu)	TTPAL (K190E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613714	NM_001039199.3(TTPAL):c.667G>T (p.Val223Phe)	TTPAL (V223F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358292	NM_001039199.3(TTPAL):c.801A>C (p.Arg267Ser)	TTPAL (R233S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184672	NM_001039199.3(TTPAL):c.838G>A (p.Glu280Lys)	TTPAL (E280K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345132	NM_001039199.3(TTPAL):c.862G>A (p.Ala288Thr)	TTPAL (A288T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330162	NM_001039199.3(TTPAL):c.892G>A (p.Val298Met)	TTPAL (V264M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570278	NM_001039199.3(TTPAL):c.965C>T (p.Thr322Ile)	TTPAL (T288I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance