BBC3[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2456891	NM_014417.5(BBC3):c.*94C>T	BBC3 (T100I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3133131	NM_014417.5(BBC3):c.*64C>G	BBC3 (T90S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3133129	NM_014417.5(BBC3):c.*57C>T	BBC3 (P248S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 770466	NM_014417.5(BBC3):c.*23C>T	BBC3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 3133128	NM_014417.5(BBC3):c.497C>T (p.Ser166Leu)	BBC3 (S104L +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2595454	NM_014417.5(BBC3):c.485G>A (p.Arg162Gln)	BBC3 (R162Q +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2211520	NM_001127240.3(BBC3):c.40C>A (p.Gln14Lys)	BBC3 (Q14K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391114	NM_001127240.3(BBC3):c.13A>G (p.Met5Val)	BBC3 (M5V)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar