"Ambry Genetics"[submitter] AND "LHX9"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2600033	NM_020204.3(LHX9):c.52C>G (p.Pro18Ala)	LHX9 (P18A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2360801	NM_020204.3(LHX9):c.136C>A (p.Arg46Ser)	LHX9 (R37S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457045	NM_020204.3(LHX9):c.152C>T (p.Ala51Val)	LHX9 (A42V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595296	NM_020204.3(LHX9):c.185C>G (p.Pro62Arg)	LHX9 (P53R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494497	NM_020204.3(LHX9):c.596T>C (p.Leu199Pro)	LHX9 (L190P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315114	NM_020204.3(LHX9):c.641C>T (p.Pro214Leu)	LHX9 (P220L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2543225	NM_020204.3(LHX9):c.791C>T (p.Ser264Leu)	LHX9 (S255L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 985541	NM_020204.3(LHX9):c.947A>G (p.Gln316Arg)	LHX9 (Q307R +1 more)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2359124	NM_020204.3(LHX9):c.983G>A (p.Arg328Gln)	LHX9 (R319Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2280675	NM_020204.3(LHX9):c.1033C>T (p.Pro345Ser)	LHX9 (P345S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2521226	NM_020204.3(LHX9):c.1090G>C (p.Asp364His)	LHX9 (D364H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2511049	NM_020204.3(LHX9):c.1096A>T (p.Thr366Ser)	LHX9 (T357S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2493542	NM_020204.3(LHX9):c.1097C>A (p.Thr366Asn)	LHX9 (T366N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance