KLK8[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3115884	NM_007196.4(KLK8):c.761A>C (p.Lys254Thr)	KLK8 (K299T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2529023	NM_007196.4(KLK8):c.730A>G (p.Asn244Asp)	KLK8 (N244D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115883	NM_007196.4(KLK8):c.709G>T (p.Asp237Tyr)	KLK8 (D116Y +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2313461	NM_007196.4(KLK8):c.623G>A (p.Cys208Tyr)	KLK8 (C208Y +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257202	NM_007196.4(KLK8):c.604A>G (p.Ser202Gly)	KLK8 (S61G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115880	NM_007196.4(KLK8):c.553G>A (p.Glu185Lys)	KLK8 (E185K +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3115879	NM_007196.4(KLK8):c.451A>C (p.Lys151Gln)	KLK8 (K151Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289089	NM_007196.4(KLK8):c.419G>A (p.Ser140Asn)	KLK8 (S140N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2552815	NM_007196.4(KLK8):c.331A>G (p.Ser111Gly)	KLK8 (S111G +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2324474	NM_007196.4(KLK8):c.143C>T (p.Ala48Val)	KLK8 (A93V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3289087	NM_007196.4(KLK8):c.121C>T (p.Pro41Ser)	KLK8 (P86S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2366487	NM_007196.4(KLK8):c.71-18C>G	KLK8 (P63R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295683	NM_007196.4(KLK8):c.71-87C>T	KLK8 (P40L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3115882	NM_007196.4(KLK8):c.71-132G>T	KLK8 (C25F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289088	NM_007196.4(KLK8):c.55G>C (p.Gly19Arg)	KLK8 (G19R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2352034	NM_007196.4(KLK8):c.38T>C (p.Met13Thr)	KLK8 (M13T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3289085	NM_007196.4(KLK8):c.14G>A (p.Arg5Gln)	KLK8 (R5Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3115878	NM_007196.4(KLK8):c.11C>A (p.Pro4His)	KLK8 (P4H)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2607230	NM_007196.4(KLK8):c.10C>A (p.Pro4Thr)	KLK8 (P4T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance