Related gene-specific medical variations for Gene (Select 9175) - ClinVar

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Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3293017	NM_004721.5(MAP3K13):c.1738A>C (p.Ser580Arg)	LOC126806894, MAP3K13 (S373R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293016	NM_004721.5(MAP3K13):c.2207G>A (p.Arg736Lys)	LOC126806894, MAP3K13 (R529K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293015	NM_004721.5(MAP3K13):c.2513G>A (p.Cys838Tyr)	LOC126806895, MAP3K13 (C838Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293013	NM_004721.5(MAP3K13):c.2399C>T (p.Ala800Val)	LOC126806894, MAP3K13 (A800V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3293011	NM_004721.5(MAP3K13):c.2674A>G (p.Thr892Ala)	LOC126806895, MAP3K13 (T685A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122869	NM_004721.5(MAP3K13):c.2516T>C (p.Ile839Thr)	LOC126806895, MAP3K13 (I632T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122867	NM_004721.5(MAP3K13):c.2383C>T (p.Leu795Phe)	LOC126806894, MAP3K13 (L795F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122866	NM_004721.5(MAP3K13):c.2377T>C (p.Ser793Pro)	LOC126806894, MAP3K13 (S586P +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3122865	NM_004721.5(MAP3K13):c.2252T>A (p.Val751Glu)	LOC126806894, MAP3K13 (V544E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122864	NM_004721.5(MAP3K13):c.2020G>A (p.Gly674Ser)	LOC126806894, MAP3K13 (G674S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122863	NM_004721.5(MAP3K13):c.1885C>A (p.Pro629Thr)	LOC126806894, MAP3K13 (P422T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122862	NM_004721.5(MAP3K13):c.1843T>A (p.Ser615Thr)	LOC126806894, MAP3K13 (S408T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122861	NM_004721.5(MAP3K13):c.1765C>T (p.Arg589Cys)	LOC126806894, MAP3K13 (R589C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623158	NM_004721.5(MAP3K13):c.2293C>A (p.Pro765Thr)	LOC126806894, MAP3K13 (P558T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614623	NM_004721.5(MAP3K13):c.1772G>A (p.Arg591His)	LOC126806894, MAP3K13 (R591H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613828	NM_004721.5(MAP3K13):c.1958A>G (p.His653Arg)	LOC126806894, MAP3K13 (H446R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561283	NM_004721.5(MAP3K13):c.2077G>A (p.Gly693Ser)	LOC126806894, MAP3K13 (G486S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543746	NM_004721.5(MAP3K13):c.2647G>A (p.Glu883Lys)	LOC126806895, MAP3K13 (E883K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469673	NM_004721.5(MAP3K13):c.2081C>T (p.Ser694Leu)	LOC126806894, MAP3K13 (S487L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411515	NM_004721.5(MAP3K13):c.2296C>G (p.Leu766Val)	LOC126806894, MAP3K13 (L766V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395076	NM_004721.5(MAP3K13):c.2371G>A (p.Gly791Ser)	LOC126806894, MAP3K13 (G584S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351820	NM_004721.5(MAP3K13):c.1945T>C (p.Ser649Pro)	LOC126806894, MAP3K13 (S649P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351367	NM_004721.5(MAP3K13):c.2743C>T (p.Arg915Cys)	LOC126806895, MAP3K13 (R915C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322762	NM_004721.5(MAP3K13):c.1754G>A (p.Arg585Gln)	LOC126806894, MAP3K13 (R585Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322056	NM_004721.5(MAP3K13):c.2594A>G (p.Asp865Gly)	LOC126806895, MAP3K13 (D658G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290438	NM_004721.5(MAP3K13):c.1766G>A (p.Arg589His)	LOC126806894, MAP3K13 (R589H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284826	NM_004721.5(MAP3K13):c.1954C>T (p.His652Tyr)	LOC126806894, MAP3K13 (H445Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254178	NM_004721.5(MAP3K13):c.2638C>T (p.Arg880Cys)	LOC126806895, MAP3K13 (R673C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225164	NM_004721.5(MAP3K13):c.2417G>A (p.Arg806Lys)	LOC126806894, MAP3K13 (R599K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 29