"Ambry Genetics"[submitter] AND "LDLRAD4"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3118291	NM_001378100.1(LDLRAD4):c.86C>T (p.Ser29Leu)	LDLRAD4 (S29L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2603046	NM_001378100.1(LDLRAD4):c.193T>C (p.Phe65Leu)	LDLRAD4 (F28L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118288	NM_001378100.1(LDLRAD4):c.299C>T (p.Pro100Leu)	LDLRAD4 (P53L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118289	NM_001378100.1(LDLRAD4):c.311G>A (p.Arg104Gln)	LDLRAD4 (R104Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288317	NM_001378100.1(LDLRAD4):c.332C>T (p.Pro111Leu)	LDLRAD4 (P34L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290412	NM_001378100.1(LDLRAD4):c.364G>A (p.Ala122Thr)	LDLRAD4 (A45T +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2613695	NM_001378100.1(LDLRAD4):c.380G>A (p.Gly127Asp)	LDLRAD4 (G80D +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2412049	NM_001378100.1(LDLRAD4):c.386C>T (p.Ser129Leu)	LDLRAD4 (S31L +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2301656	NM_001378100.1(LDLRAD4):c.407G>A (p.Arg136Gln)	LDLRAD4 (R118Q +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568302	NM_001378100.1(LDLRAD4):c.451C>T (p.Arg151Cys)	LDLRAD4 (R114C +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320536	NM_001378100.1(LDLRAD4):c.491A>G (p.His164Arg)	LDLRAD4 (H109R +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533375	NM_001378100.1(LDLRAD4):c.700A>T (p.Asn234Tyr)	LDLRAD4 (N136Y +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290413	NM_001378100.1(LDLRAD4):c.737G>A (p.Gly246Glu)	LDLRAD4 (G148E +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118290	NM_001378100.1(LDLRAD4):c.767G>T (p.Ser256Ile)	LDLRAD4 (S179I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance