"Ambry Genetics"[submitter] AND "TRAPPC13"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2591405	NM_024941.4(TRAPPC13):c.157G>A (p.Val53Ile)	TRAPPC13 (V53I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329520	NM_024941.4(TRAPPC13):c.180G>T (p.Met60Ile)	TRAPPC13 (M60I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263465	NM_024941.4(TRAPPC13):c.256G>A (p.Val86Ile)	TRAPPC13 (V86I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324288	NM_024941.4(TRAPPC13):c.347A>G (p.Asn116Ser)	TRAPPC13 (N116S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181983	NM_024941.4(TRAPPC13):c.348T>A (p.Asn116Lys)	TRAPPC13 (N116K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316316	NM_024941.4(TRAPPC13):c.416T>C (p.Ile139Thr)	TRAPPC13 (I139T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368599	NM_024941.4(TRAPPC13):c.613C>A (p.Pro205Thr)	TRAPPC13 (P199T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394962	NM_024941.4(TRAPPC13):c.616A>G (p.Met206Val)	TRAPPC13 (M200V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181984	NM_024941.4(TRAPPC13):c.746G>A (p.Arg249His)	TRAPPC13 (R86H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222339	NM_024941.4(TRAPPC13):c.778G>A (p.Glu260Lys)	TRAPPC13 (E97K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402726	NM_024941.4(TRAPPC13):c.870G>T (p.Arg290Ser)	TRAPPC13 (R127S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253340	NM_024941.4(TRAPPC13):c.971A>G (p.His324Arg)	TRAPPC13 (H324R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546850	NM_024941.4(TRAPPC13):c.1096T>C (p.Ser366Pro)	TRAPPC13 (S204P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181980	NM_024941.4(TRAPPC13):c.1210G>A (p.Ala404Thr)	TRAPPC13 (A399T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181981	NM_024941.4(TRAPPC13):c.1225G>C (p.Val409Leu)	TRAPPC13 (V404L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance