"Ambry Genetics"[submitter] AND "KLK15"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2595487	NM_017509.4(KLK15):c.759G>A (p.Met253Ile)	KLK15 (M252I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2537100	NM_017509.4(KLK15):c.748A>G (p.Arg250Gly)	KLK15 (R250G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2301768	NM_017509.4(KLK15):c.716A>G (p.Tyr239Cys)	KLK15 (Y238C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2384332	NM_017509.4(KLK15):c.682G>A (p.Val228Ile)	KLK15 (V227I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115843	NM_017509.4(KLK15):c.665T>C (p.Ile222Thr)	KLK15 (I222T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555160	NM_017509.4(KLK15):c.574A>G (p.Met192Val)	KLK15 (M191V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115842	NM_017509.4(KLK15):c.559C>T (p.Arg187Cys)	KLK15 (R186C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115841	NM_017509.4(KLK15):c.469C>T (p.Pro157Ser)	KLK15 (P156S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243217	NM_017509.4(KLK15):c.359C>G (p.Pro120Arg)	KLK15 (P119R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595639	NM_017509.4(KLK15):c.355A>C (p.Asn119His)	KLK15 (N118H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115839	NM_017509.4(KLK15):c.242A>G (p.Asp81Gly)	KLK15 (D81G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558205	NM_017509.4(KLK15):c.238C>A (p.Arg80Ser)	KLK15 (R79S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289073	NM_017509.4(KLK15):c.209T>C (p.Val70Ala)	KLK15 (V69A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289072	NM_017509.4(KLK15):c.207A>T (p.Arg69Ser)	KLK15 (R68S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289074	NM_017509.4(KLK15):c.204G>C (p.Met68Ile)	KLK15 (M67I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115838	NM_017509.4(KLK15):c.188G>A (p.Cys63Tyr)	KLK15 (C62Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251268	NM_017509.4(KLK15):c.131G>A (p.Arg44His)	KLK15 (R43H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115844	NM_017509.4(KLK15):c.98A>G (p.Gln33Arg)	KLK15 (Q32R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395259	NM_017509.4(KLK15):c.55G>A (p.Gly19Ser)	KLK15 (G19S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance