LDB1[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2297369	NM_001113407.3(LDB1):c.1199G>A (p.Ser400Asn)	LDB1 (S398N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397323	NM_001113407.3(LDB1):c.1125G>C (p.Glu375Asp)	LDB1 (E339D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118207	NM_001113407.3(LDB1):c.1057G>A (p.Glu353Lys)	LDB1 (E351K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118206	NM_001113407.3(LDB1):c.1015G>A (p.Val339Met)	LDB1 (V303M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332255	NM_001113407.3(LDB1):c.919A>G (p.Met307Val)	LDB1 (M307V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485934	NM_001113407.3(LDB1):c.910G>T (p.Gly304Cys)	LDB1 (G268C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544080	NM_001113407.3(LDB1):c.868C>T (p.Arg290Cys)	LDB1 (R254C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290032	NM_001113407.3(LDB1):c.773G>A (p.Arg258His)	LDB1 (R222H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118208	NM_001113407.3(LDB1):c.710A>G (p.Asn237Ser)	LDB1 (N201S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481126	NM_001113407.3(LDB1):c.666G>T (p.Met222Ile)	LDB1 (M186I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118209	NM_001113407.3(LDB1):c.76G>A (p.Gly26Ser)	LDB1 (G26S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance