"PreventionGenetics, part of Exact Sciences"[submitter] AND "DIPK2B"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3054407	NM_176819.4(DIPK2B):c.1171G>C (p.Asp391His)	DIPK2B (D391H)	Single nucleotide variant (missense variant)	DIPK2B-related disorder	GLikely benign
Select item 3050838	NM_176819.4(DIPK2B):c.1096C>T (p.Leu366=)	DIPK2B	Single nucleotide variant (synonymous variant)	DIPK2B-related disorder	GLikely benign
Select item 711138	NM_176819.4(DIPK2B):c.1092G>A (p.Lys364=)	DIPK2B	Single nucleotide variant (synonymous variant)	DIPK2B-related disorder +1 more	GBenign
Select item 3049454	NM_176819.4(DIPK2B):c.1020C>T (p.Ser340=)	DIPK2B	Single nucleotide variant (synonymous variant)	DIPK2B-related disorder	GLikely benign
Select item 3033826	NM_176819.4(DIPK2B):c.428G>T (p.Arg143Leu)	DIPK2B (R143L)	Single nucleotide variant (missense variant)	DIPK2B-related disorder	GBenign
Select item 3059778	NM_176819.4(DIPK2B):c.383G>A (p.Arg128Lys)	DIPK2B (R128K)	Single nucleotide variant (missense variant)	DIPK2B-related disorder	GBenign
Select item 3046016	NM_176819.4(DIPK2B):c.313T>C (p.Ser105Pro)	DIPK2B (S105P)	Single nucleotide variant (missense variant)	DIPK2B-related disorder	GBenign

ClinVar