"PreventionGenetics, part of Exact Sciences"[submitter] AND "KLHL15"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2630901	NM_030624.3(KLHL15):c.1777C>A (p.Pro593Thr)	KLHL15 (P593T)	Single nucleotide variant (missense variant)	KLHL15-related condition	GUncertain significance
Select item 714922	NM_030624.3(KLHL15):c.1695G>A (p.Pro565=)	KLHL15	Single nucleotide variant (synonymous variant)	KLHL15-related condition +1 more	GBenign
Select item 2630796	NM_030624.3(KLHL15):c.663T>G (p.Asn221Lys)	KLHL15, LOC114022706 (N221K)	Single nucleotide variant (missense variant)	KLHL15-related condition	GUncertain significance
Select item 3034066	NM_030624.3(KLHL15):c.441C>T (p.Ile147=)	KLHL15	Single nucleotide variant (synonymous variant)	KLHL15-related condition	GLikely benign
Select item 3060224	NM_030624.3(KLHL15):c.123G>A (p.Gln41=)	KLHL15	Single nucleotide variant (synonymous variant)	KLHL15-related condition	GLikely benign

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