"Ambry Genetics"[submitter] AND "LBX2"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2341424	NM_001282430.2(LBX2):c.584A>C (p.Gln195Pro)	LBX2, LOC129934135 (Q191P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461461	NM_001282430.2(LBX2):c.542C>T (p.Ala181Val)	LBX2 (A177V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250814	NM_001282430.2(LBX2):c.535G>A (p.Gly179Ser)	LBX2 (G175S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290227	NM_001282430.2(LBX2):c.478G>A (p.Glu160Lys)	LBX2 (E156K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344896	NM_001282430.2(LBX2):c.476C>T (p.Pro159Leu)	LBX2 (P155L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570442	NM_001282430.2(LBX2):c.364C>T (p.Leu122Phe)	LBX2 (L122F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118008	NM_001282430.2(LBX2):c.260A>G (p.Lys87Arg)	LBX2 (K87R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118007	NM_001282430.2(LBX2):c.238C>T (p.Pro80Ser)	LBX2 (P80S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354645	NM_001282430.2(LBX2):c.214G>C (p.Gly72Arg)	LBX2 (G68R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354897	NM_001009812.2(LBX2):c.43G>C (p.Gly15Arg)	LBX2, LBX2-AS1 (G15R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance