"Ambry Genetics"[submitter] AND "COLEC10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2535984	NM_006438.5(COLEC10):c.73A>G (p.Ser25Gly)	COLEC10, LOC101927513 +1 more (S25G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2258879	NM_006438.5(COLEC10):c.106G>A (p.Ala36Thr)	COLEC10, LOC101927513 +1 more (A36T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2222250	NM_006438.5(COLEC10):c.410G>A (p.Arg137Gln)	COLEC10 (R68Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361697	NM_006438.5(COLEC10):c.497A>G (p.Glu166Gly)	COLEC10 (E166G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277522	NM_006438.5(COLEC10):c.511G>C (p.Glu171Gln)	COLEC10 (E102Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489263	NM_006438.5(COLEC10):c.784T>G (p.Cys262Gly)	COLEC10 (C262G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar