"PreventionGenetics, part of Exact Sciences"[submitter] AND "CABP4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1108202	NM_145200.5(CABP4):c.108G>A (p.Pro36=)	CABP4	Single nucleotide variant (5 prime UTR variant +3 more)	CABP4-related disorder +1 more	GLikely benign
Select item 879899	NM_145200.5(CABP4):c.246C>A (p.Gly82=)	CABP4	Single nucleotide variant (5 prime UTR variant +3 more)	CABP4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1169609	NM_145200.5(CABP4):c.378G>A (p.Leu126=)	CABP4	Single nucleotide variant (synonymous variant)	CABP4-related disorder +1 more	GBenign/Likely benign
Select item 2048789	NM_145200.5(CABP4):c.384C>T (p.Pro128=)	CABP4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 262579	NM_145200.5(CABP4):c.541+7_541+8delinsGC	CABP4	Indel (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2193692	NM_145200.5(CABP4):c.541+8A>T	CABP4	Single nucleotide variant (intron variant)	CABP4-related disorder +1 more	GLikely benign
Select item 262580	NM_145200.5(CABP4):c.800-5C>T	CABP4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign

ClinVar