"Ambry Genetics"[submitter] AND "KLK11"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2352846	NM_001136032.3(KLK11):c.737C>T (p.Thr246Met)	KLK11 (T246M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462274	NM_001136032.3(KLK11):c.701C>T (p.Thr234Met)	KLK11 (T234M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2337637	NM_001136032.3(KLK11):c.483G>C (p.Leu161Phe)	KLK11 (L193F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294571	NM_001136032.3(KLK11):c.479C>T (p.Thr160Ile)	KLK11 (T160I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3115810	NM_001136032.3(KLK11):c.380G>A (p.Arg127Gln)	KLK11 (R127Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3115809	NM_001136032.3(KLK11):c.352T>A (p.Ser118Thr)	KLK11 (S118T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2512691	NM_001136032.3(KLK11):c.326A>G (p.Asn109Ser)	KLK11 (N141S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357541	NM_001136032.3(KLK11):c.296A>G (p.Asn99Ser)	KLK11 (N99S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3289061	NM_001136032.3(KLK11):c.292T>C (p.Phe98Leu)	KLK11 (F123L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588341	NM_001136032.3(KLK11):c.289G>A (p.Gly97Ser)	KLK11 (G129S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378505	NM_001136032.3(KLK11):c.200G>A (p.Arg67His)	KLK11 (R67H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3115807	NM_001136032.3(KLK11):c.146C>T (p.Ala49Val)	KLK11 (A49V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2268711	NM_001136032.3(KLK11):c.79G>A (p.Glu27Lys)	KLK11 (E59K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3115811	NM_001136032.3(KLK11):c.-11C>G	KLK11 (P29R)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2462684	NM_001136032.3(KLK11):c.-11C>T	KLK11 (P29L)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622924	NM_001136032.3(KLK11):c.-21C>G	KLK11 (R26G)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2255284	NM_144947.3(KLK11):c.52A>G (p.Thr18Ala)	KLK11 (T18A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3115808	NM_144947.3(KLK11):c.41G>A (p.Gly14Asp)	KLK11 (G14D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2338538	NM_144947.3(KLK11):c.25G>T (p.Asp9Tyr)	KLK11 (D9Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance