"Ambry Genetics"[submitter] AND "LOC126861158"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2268125	NM_145117.5(NAV2):c.3911G>T (p.Gly1304Val)	LOC126861158, NAV2 +1 more (G390V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177116	NM_145117.5(NAV2):c.3922A>G (p.Thr1308Ala)	LOC126861158, NAV2 +1 more (T394A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219229	NM_145117.5(NAV2):c.4022C>T (p.Pro1341Leu)	LOC126861158, NAV2 +1 more (P1277L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512058	NM_145117.5(NAV2):c.4024T>A (p.Ser1342Thr)	LOC126861158, NAV2 +1 more (S1342T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298512	NM_145117.5(NAV2):c.4097C>T (p.Pro1366Leu)	LOC126861158, NAV2 +1 more (P1366L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265354	NM_145117.5(NAV2):c.4124A>G (p.His1375Arg)	LOC126861158, NAV2 +1 more (H461R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366685	NM_145117.5(NAV2):c.4162G>A (p.Ala1388Thr)	LOC126861158, NAV2 +1 more (A1411T +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3298513	NM_145117.5(NAV2):c.4184G>A (p.Ser1395Asn)	LOC126861158, NAV2 +1 more (S1395N +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3177128	NM_145117.5(NAV2):c.4246A>G (p.Ile1416Val)	LOC126861158, NAV2 +1 more (I502V +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2485776	NM_145117.5(NAV2):c.4280A>G (p.Asn1427Ser)	LOC126861158, NAV2 +1 more (N1450S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312071	NM_145117.5(NAV2):c.4294C>T (p.Leu1432Phe)	LOC126861158, NAV2 +1 more (L1368F +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3298519	NM_145117.5(NAV2):c.4352A>G (p.Lys1451Arg)	LOC126861158, NAV2 +1 more (K1387R +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2617291	NM_145117.5(NAV2):c.4364C>T (p.Ser1455Leu)	LOC126861158, NAV2 +1 more (S1391L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance