Related gene-specific medical variations for Gene (Select 5900) - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312636	NM_006266.4(RALGDS):c.2183C>T (p.Pro728Leu)	LOC126860784, RALGDS (P716L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312629	NM_006266.4(RALGDS):c.151A>G (p.Thr51Ala)	LOC130002888, RALGDS (T51A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151315	NM_006266.4(RALGDS):c.44G>T (p.Gly15Val)	LOC130002888, RALGDS (G15V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151312	NM_006266.4(RALGDS):c.2422G>C (p.Val808Leu)	LOC126860784, RALGDS (V807L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151311	NM_006266.4(RALGDS):c.2311G>A (p.Ala771Thr)	LOC126860784, RALGDS (A770T +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3151310	NM_006266.4(RALGDS):c.2245A>T (p.Thr749Ser)	LOC126860784, RALGDS (T737S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151309	NM_006266.4(RALGDS):c.2101G>A (p.Gly701Arg)	LOC126860784, RALGDS (G689R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151307	NM_006266.4(RALGDS):c.122A>G (p.Asp41Gly)	LOC130002888, RALGDS (D41G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2659688	NM_006266.4(RALGDS):c.2340A>G (p.Ser780=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2600367	NM_006266.4(RALGDS):c.2012G>A (p.Arg671His)	LOC126860784, RALGDS (R670H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542447	NM_006266.4(RALGDS):c.53C>A (p.Pro18Gln)	LOC130002888, RALGDS (P18Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534516	NM_006266.4(RALGDS):c.116T>G (p.Val39Gly)	LOC130002888, RALGDS (V39G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523708	NM_006266.4(RALGDS):c.2132C>T (p.Ser711Leu)	LOC126860784, RALGDS (S656L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478175	NM_006266.4(RALGDS):c.14T>C (p.Met5Thr)	LOC130002888, RALGDS (M5T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454792	NM_006266.4(RALGDS):c.2110G>A (p.Ala704Thr)	LOC126860784, RALGDS (A649T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311215	NM_006266.4(RALGDS):c.2179G>A (p.Val727Ile)	LOC126860784, RALGDS (V715I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223985	NM_006266.4(RALGDS):c.2155G>A (p.Val719Met)	LOC126860784, RALGDS (V690M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775280	NM_006266.4(RALGDS):c.2385G>A (p.Gln795=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 742367	NM_006266.4(RALGDS):c.2064C>T (p.Ser688=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 717971	NM_006266.4(RALGDS):c.2136C>T (p.Ala712=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711898	NM_006266.4(RALGDS):c.2238C>T (p.Ser746=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709863	NM_006266.4(RALGDS):c.2154C>T (p.Asp718=)	LOC126860784, RALGDS	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 22