LIME1[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2244679	NM_017806.4(LIME1):c.10C>T (p.Pro4Ser)	LIME1 (P4S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118887	NM_017806.4(LIME1):c.76G>A (p.Ala26Thr)	LIME1 (A26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333175	NM_017806.4(LIME1):c.103G>A (p.Glu35Lys)	LIME1 (E35K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381573	NM_017806.4(LIME1):c.106G>A (p.Asp36Asn)	LIME1 (D36N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118881	NM_017806.4(LIME1):c.133C>T (p.Arg45Trp)	LIME1 (R45W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118882	NM_017806.4(LIME1):c.140A>G (p.Gln47Arg)	LIME1 (Q47R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118883	NM_017806.4(LIME1):c.155A>C (p.Gln52Pro)	LIME1 (Q52P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211362	NM_017806.4(LIME1):c.164C>A (p.Ala55Glu)	LIME1 (A55E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206179	NM_017806.4(LIME1):c.169G>A (p.Ala57Thr)	LIME1 (A57T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118884	NM_017806.4(LIME1):c.176A>C (p.Glu59Ala)	LIME1 (E59A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372243	NM_017806.4(LIME1):c.800G>A (p.Ser267Asn)	LIME1 (S267N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2596017	NM_017806.4(LIME1):c.856G>A (p.Gly286Ser)	LIME1 (G286S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance