"Ambry Genetics"[submitter] AND "SEC11A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2257875	NM_014300.4(SEC11A):c.519C>G (p.Phe173Leu)	SEC11A (F133L +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555758	NM_014300.4(SEC11A):c.451A>G (p.Ile151Val)	SEC11A (I101V +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2243119	NM_014300.4(SEC11A):c.409G>C (p.Asp137His)	SEC11A (D111H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3317009	NM_014300.4(SEC11A):c.397C>G (p.Leu133Val)	SEC11A (L107V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3159097	NM_014300.4(SEC11A):c.356C>T (p.Ala119Val)	SEC11A (A69V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2604522	NM_014300.4(SEC11A):c.55T>C (p.Tyr19His)	SEC11A (Y19H)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2483474	NM_014300.4(SEC11A):c.32G>A (p.Arg11Gln)	SEC11A (R11Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

ClinVar