"Ambry Genetics"[submitter] AND "NKAIN2"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2334102	NM_001040214.3(NKAIN2):c.13A>G (p.Ser5Gly)	NKAIN2 (S5G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609529	NM_001040214.3(NKAIN2):c.42T>G (p.Cys14Trp)	NKAIN2 (C14W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541153	NM_001040214.3(NKAIN2):c.133A>G (p.Ile45Val)	NKAIN2 (I44V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200250	NM_001040214.3(NKAIN2):c.173G>A (p.Arg58Lys)	NKAIN2 (R57K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552418	NM_001040214.3(NKAIN2):c.188C>A (p.Thr63Lys)	NKAIN2 (T63K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299847	NM_001040214.3(NKAIN2):c.340G>A (p.Gly114Arg)	NKAIN2 (G12R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286386	NM_001040214.3(NKAIN2):c.472G>A (p.Ala158Thr)	NKAIN2 (A56T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249077	NM_001040214.3(NKAIN2):c.512G>C (p.Cys171Ser)	NKAIN2 (C170S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215747	NM_001040214.3(NKAIN2):c.547G>T (p.Gly183Cys)	NKAIN2 (G116C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299848	NM_001040214.3(NKAIN2):c.619T>C (p.Ser207Pro)	NKAIN2 (S117P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance