"UNC5C-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048687	NM_003728.4(UNC5C):c.2772C>T (p.Ser924=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GLikely benign
Select item 3039977	NM_003728.4(UNC5C):c.2709T>C (p.Asp903=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GBenign
Select item 2630639	NM_003728.4(UNC5C):c.2537T>C (p.Leu846Pro)	UNC5C (L846P)	Single nucleotide variant (missense variant)	UNC5C-related condition	GUncertain significance
Select item 2654955	NM_003728.4(UNC5C):c.2521G>A (p.Ala841Thr)	UNC5C (A841T)	Single nucleotide variant (missense variant)	UNC5C-related condition +1 more	GBenign
Select item 2654956	NM_003728.4(UNC5C):c.2514G>A (p.Gly838=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition +1 more	GLikely benign
Select item 3044981	NM_003728.4(UNC5C):c.2448A>G (p.Ser816=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GLikely benign
Select item 3037433	NM_003728.4(UNC5C):c.2442C>T (p.Thr814=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GLikely benign
Select item 3057306	NM_003728.4(UNC5C):c.2221C>T (p.Leu741=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GLikely benign
Select item 3060184	NM_003728.4(UNC5C):c.2162T>C (p.Met721Thr)	UNC5C (M721T)	Single nucleotide variant (missense variant)	UNC5C-related condition	GBenign
Select item 3056866	NM_003728.4(UNC5C):c.2065C>G (p.Pro689Ala)	UNC5C (P689A)	Single nucleotide variant (missense variant)	UNC5C-related condition	GBenign
Select item 3060708	NM_003728.4(UNC5C):c.2037G>A (p.Ala679=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GBenign
Select item 3044338	NM_003728.4(UNC5C):c.2036C>T (p.Ala679Val)	UNC5C (A679V)	Single nucleotide variant (missense variant)	UNC5C-related condition	GLikely benign
Select item 3042011	NM_003728.4(UNC5C):c.1883C>A (p.Ala628Glu)	UNC5C (A628E)	Single nucleotide variant (missense variant)	UNC5C-related condition	GBenign
Select item 3041410	NM_003728.4(UNC5C):c.1882G>A (p.Ala628Thr)	UNC5C (A628T)	Single nucleotide variant (missense variant)	UNC5C-related condition	GBenign
Select item 3059577	NM_003728.4(UNC5C):c.1812A>C (p.Pro604=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GBenign
Select item 1257938	NM_003728.4(UNC5C):c.1614G>A (p.Ser538=)	LOC126807113, UNC5C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2654957	NM_003728.4(UNC5C):c.1524G>A (p.Ser508=)	LOC126807113, UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition +1 more	GLikely benign
Select item 3057411	NM_003728.4(UNC5C):c.1494G>A (p.Thr498=)	LOC126807113, UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GLikely benign
Select item 2654958	NM_003728.4(UNC5C):c.933G>A (p.Thr311=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition +1 more	GLikely benign
Select item 3056877	NM_003728.4(UNC5C):c.801G>A (p.Thr267=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GBenign
Select item 3033334	NM_003728.4(UNC5C):c.319G>C (p.Val107Leu)	UNC5C (V107L)	Single nucleotide variant (missense variant)	UNC5C-related condition	GBenign
Select item 3059355	NM_003728.4(UNC5C):c.291T>C (p.Ser97=)	UNC5C	Single nucleotide variant (synonymous variant)	UNC5C-related condition	GBenign
Select item 3034732	NM_003728.4(UNC5C):c.124+6G>A	UNC5C	Single nucleotide variant (intron variant)	UNC5C-related condition	GLikely benign

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Items: 23