LCE1F[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2224735	NM_178354.3(LCE1F):c.53C>T (p.Pro18Leu)	LCE1F (P18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616953	NM_178354.3(LCE1F):c.59G>A (p.Cys20Tyr)	LCE1F (C20Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406100	NM_178354.3(LCE1F):c.62C>T (p.Pro21Leu)	LCE1F (P21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254388	NM_178354.3(LCE1F):c.115C>T (p.Pro39Ser)	LCE1F (P39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537623	NM_178354.3(LCE1F):c.136G>A (p.Val46Ile)	LCE1F (V46I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403817	NM_178354.3(LCE1F):c.211G>C (p.Gly71Arg)	LCE1F (G71R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616952	NM_178354.3(LCE1F):c.212G>A (p.Gly71Glu)	LCE1F (G71E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2639338	NM_178354.3(LCE1F):c.225T>C (p.Cys75=)	LCE1F	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639339	NM_178354.3(LCE1F):c.243A>G (p.Arg81=)	LCE1F	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639340	NM_178354.3(LCE1F):c.246G>C (p.Arg82=)	LCE1F	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639341	NM_178354.3(LCE1F):c.249T>C (p.Arg83=)	LCE1F	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3118041	NM_178354.3(LCE1F):c.260G>A (p.Arg87His)	LCE1F (R87H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309606	NM_178354.3(LCE1F):c.302C>T (p.Ala101Val)	LCE1F (A101V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464298	NM_178354.3(LCE1F):c.313T>G (p.Cys105Gly)	LCE1F (C105G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290255	NM_178354.3(LCE1F):c.319G>A (p.Gly107Arg)	LCE1F (G107R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118042	NM_178354.3(LCE1F):c.322G>T (p.Gly108Trp)	LCE1F (G108W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407060	NM_178354.3(LCE1F):c.323G>C (p.Gly108Ala)	LCE1F (G108A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537454	NM_178354.3(LCE1F):c.325G>T (p.Gly109Cys)	LCE1F (G109C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance