Related gene-specific medical variations for Gene (Select 5918) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312819	NM_206963.2(RARRES1):c.292G>A (p.Gly98Arg)	LOC126806859, RARRES1 (G98R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151658	NM_206963.2(RARRES1):c.34T>C (p.Trp12Arg)	LOC100287290, RARRES1 (W12R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3151657	NM_206963.2(RARRES1):c.295T>C (p.Cys99Arg)	LOC126806859, RARRES1 (C99R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404036	NM_206963.2(RARRES1):c.124G>C (p.Asp42His)	LOC129937823, RARRES1 (D42H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381831	NM_206963.2(RARRES1):c.125A>C (p.Asp42Ala)	LOC129937823, RARRES1 (D42A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381829	NM_206963.2(RARRES1):c.118T>G (p.Ser40Ala)	LOC129937823, RARRES1 (S40A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356681	NM_206963.2(RARRES1):c.316A>G (p.Ser106Gly)	LOC126806859, RARRES1 (S106G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344505	NM_206963.2(RARRES1):c.34T>A (p.Trp12Arg)	LOC100287290, RARRES1 (W12R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2288695	NM_206963.2(RARRES1):c.307G>A (p.Val103Met)	LOC126806859, RARRES1 (V103M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273772	NM_206963.2(RARRES1):c.137C>G (p.Pro46Arg)	LOC129937823, RARRES1 (P46R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance