"PreventionGenetics, part of Exact Sciences"[submitter] AND "KLK3"[gen - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035909	NM_001648.2(KLK3):c.47-9C>G	KLK3	Single nucleotide variant (intron variant)	KLK3-related disorder	GLikely benign
Select item 3059788	NM_001648.2(KLK3):c.48T>C (p.Gly16=)	KLK3	Single nucleotide variant (synonymous variant)	KLK3-related disorder	GBenign
Select item 3060459	NM_001648.2(KLK3):c.54A>G (p.Ala18=)	KLK3	Single nucleotide variant (synonymous variant)	KLK3-related disorder	GBenign
Select item 3056767	NM_001648.2(KLK3):c.117G>A (p.Gln39=)	KLK3	Single nucleotide variant (synonymous variant)	KLK3-related disorder	GBenign
Select item 3057076	NM_001648.2(KLK3):c.237C>T (p.Ser79=)	KLK3	Single nucleotide variant (synonymous variant +1 more)	KLK3-related disorder	GBenign
Select item 3052696	NM_001648.2(KLK3):c.373C>T (p.Arg125Cys)	KLK3 (R125C +1 more)	Single nucleotide variant (missense variant)	KLK3-related disorder	GBenign
Select item 3056698	NM_001648.2(KLK3):c.394C>A (p.Leu132Ile)	KLK3 (L132I +1 more)	Single nucleotide variant (missense variant)	KLK3-related disorder	GBenign
Select item 3041951	NM_001648.2(KLK3):c.447G>A (p.Gly149=)	KLK3	Single nucleotide variant (synonymous variant)	KLK3-related disorder	GLikely benign
Select item 3042419	NM_001648.2(KLK3):c.459C>T (p.Tyr153=)	KLK3	Single nucleotide variant (synonymous variant)	KLK3-related disorder	GLikely benign
Select item 3038816	NM_001648.2(KLK3):c.629C>G (p.Ser210Trp)	KLK3 (S167W +1 more)	Single nucleotide variant (missense variant)	KLK3-related disorder	GLikely benign
Select item 3055674	NM_001648.2(KLK3):c.631-425C>T	KLK3	Single nucleotide variant (synonymous variant +1 more)	KLK3-related disorder	GBenign
Select item 3057205	NM_001648.2(KLK3):c.631-424G>A	KLK3 (E217K)	Single nucleotide variant (missense variant +1 more)	KLK3-related disorder	GBenign
Select item 3043948	NM_001648.2(KLK3):c.645C>G (p.Gly215=)	KLK3	Single nucleotide variant (3 prime UTR variant +1 more)	KLK3-related disorder	GLikely benign
Select item 3039521	NM_001648.2(KLK3):c.699A>G (p.Pro233=)	KLK3	Single nucleotide variant (3 prime UTR variant +1 more)	KLK3-related disorder	GBenign