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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043898	NM_001742.4(CALCR):c.1369G>A (p.Glu457Lys)	CALCR (E457K +1 more)	Single nucleotide variant (missense variant)	CALCR-related condition	GLikely benign
Select item 17636	NM_001742.4(CALCR):c.1340T>C (p.Leu447Pro)	CALCR (L447P +1 more)	Single nucleotide variant (missense variant)	CALCR-related condition +1 more	GBenign
Select item 3049696	NM_001742.4(CALCR):c.993T>C (p.His331=)	CALCR	Single nucleotide variant (synonymous variant)	CALCR-related condition	GLikely benign
Select item 3033180	NM_001742.4(CALCR):c.524G>A (p.Ser175Asn)	CALCR (S175N +1 more)	Single nucleotide variant (missense variant)	CALCR-related condition	GBenign
Select item 3039657	NM_001742.4(CALCR):c.478A>G (p.Ile160Val)	CALCR (I160V)	Single nucleotide variant (missense variant)	CALCR-related condition	GLikely benign
Select item 717880	NM_001742.4(CALCR):c.127G>A (p.Val43Ile)	CALCR (V43I)	Single nucleotide variant (missense variant)	CALCR-related condition +1 more	GBenign/Likely benign
Select item 3035666	NM_001742.4(CALCR):c.81A>G (p.Ser27=)	CALCR	Single nucleotide variant (synonymous variant)	CALCR-related condition	GLikely benign
Select item 1274950	NM_001742.4(CALCR):c.-6T>C	CALCR	Single nucleotide variant (5 prime UTR variant)	CALCR-related condition +1 more	GBenign

ClinVar