"PreventionGenetics, part of Exact Sciences"[submitter] AND "KIAA0232" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052068	NM_014743.3(KIAA0232):c.48C>G (p.Ser16Arg)	KIAA0232 (S16R)	Single nucleotide variant (missense variant)	KIAA0232-related disorder	GLikely benign
Select item 2632683	NM_014743.3(KIAA0232):c.158A>T (p.Asp53Val)	KIAA0232 (D53V)	Single nucleotide variant (missense variant)	KIAA0232-related disorder	GUncertain significance
Select item 782440	NM_014743.3(KIAA0232):c.1106C>T (p.Pro369Leu)	KIAA0232 (P369L)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3033519	NM_014743.3(KIAA0232):c.1633A>G (p.Thr545Ala)	KIAA0232 (T545A)	Single nucleotide variant (missense variant)	KIAA0232-related disorder	GLikely benign
Select item 3051427	NM_014743.3(KIAA0232):c.1913T>C (p.Ile638Thr)	KIAA0232 (I638T)	Single nucleotide variant (missense variant)	KIAA0232-related disorder	GLikely benign
Select item 3047482	NM_014743.3(KIAA0232):c.3688T>G (p.Cys1230Gly)	KIAA0232 (C1230G)	Single nucleotide variant (missense variant)	KIAA0232-related disorder	GLikely benign

ClinVar