"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "CDIN1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1163569	NM_001321759.2(CDIN1):c.46G>A (p.Val16Met)	CDIN1 (V16M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3380256	NM_001321759.2(CDIN1):c.91_93del (p.Arg31del)	CDIN1 (R31del)	Deletion (5 prime UTR variant)	not provided	GUncertain significance
Select item 2683789	NM_001321759.2(CDIN1):c.307A>T (p.Ile103Leu)	CDIN1 (I103L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1163570	NM_001321759.2(CDIN1):c.430A>G (p.Ile144Val)	CDIN1 (I107V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 692136	NM_001321759.2(CDIN1):c.707A>G (p.Tyr236Cys)	CDIN1 (Y113C +4 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia type type 1B +1 more	GUncertain significance
Select item 2439610	NM_001321759.2(CDIN1):c.812C>A (p.Thr271Lys)	CDIN1 (T148K +4 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia type type 1B +1 more	GUncertain significance

ClinVar