Related gene-specific medical variations for Gene (Select 10036) - ClinVar

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Links from Gene

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330755	NM_025241.3(UBXN6):c.547G>A (p.Asp183Asn)	CHAF1A, UBXN6 (D183N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330754	NM_025241.3(UBXN6):c.883C>T (p.Leu295Phe)	CHAF1A, UBXN6 (L295F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330753	NM_025241.3(UBXN6):c.1033G>T (p.Asp345Tyr)	CHAF1A, UBXN6 (D345Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330751	NM_025241.3(UBXN6):c.1307C>G (p.Ala436Gly)	CHAF1A, UBXN6 (A436G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330750	NM_025241.3(UBXN6):c.1252A>G (p.Ile418Val)	CHAF1A, UBXN6 (I365V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185930	NM_025241.3(UBXN6):c.950T>C (p.Leu317Pro)	CHAF1A, UBXN6 (L264P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185929	NM_025241.3(UBXN6):c.937C>T (p.Arg313Trp)	CHAF1A, UBXN6 (R313W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185927	NM_025241.3(UBXN6):c.879C>A (p.Phe293Leu)	CHAF1A, UBXN6 (F293L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185926	NM_025241.3(UBXN6):c.853C>A (p.Gln285Lys)	CHAF1A, UBXN6 (Q285K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185925	NM_025241.3(UBXN6):c.802G>A (p.Ala268Thr)	CHAF1A, UBXN6 (A215T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185924	NM_025241.3(UBXN6):c.788C>T (p.Ala263Val)	CHAF1A, UBXN6 (A210V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185923	NM_025241.3(UBXN6):c.617A>G (p.Glu206Gly)	CHAF1A, UBXN6 (E206G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185921	NM_025241.3(UBXN6):c.1272G>C (p.Glu424Asp)	CHAF1A, UBXN6 (E424D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185920	NM_025241.3(UBXN6):c.1237G>A (p.Ala413Thr)	CHAF1A, UBXN6 (A360T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649036	NM_025241.3(UBXN6):c.645C>T (p.His215=)	CHAF1A, UBXN6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2614187	NM_025241.3(UBXN6):c.1090G>T (p.Gly364Trp)	CHAF1A, UBXN6 (G311W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604896	NM_025241.3(UBXN6):c.938G>A (p.Arg313Gln)	CHAF1A, UBXN6 (R313Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517412	NM_025241.3(UBXN6):c.564C>A (p.His188Gln)	CHAF1A, UBXN6 (H135Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512709	NM_025241.3(UBXN6):c.799C>T (p.Arg267Cys)	CHAF1A, UBXN6 (R267C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467676	NM_025241.3(UBXN6):c.737C>G (p.Thr246Ser)	CHAF1A, UBXN6 (T193S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454285	NM_025241.3(UBXN6):c.568G>A (p.Glu190Lys)	CHAF1A, UBXN6 (E137K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397973	NM_025241.3(UBXN6):c.574G>A (p.Glu192Lys)	CHAF1A, UBXN6 (E139K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392511	NM_025241.3(UBXN6):c.488C>T (p.Thr163Met)	CHAF1A, UBXN6 (T110M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373265	NM_025241.3(UBXN6):c.662T>C (p.Ile221Thr)	CHAF1A, UBXN6 (I168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365281	NM_025241.3(UBXN6):c.938G>T (p.Arg313Leu)	CHAF1A, UBXN6 (R313L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2364942	NM_025241.3(UBXN6):c.1240G>A (p.Val414Met)	CHAF1A, UBXN6 (V361M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351670	NM_025241.3(UBXN6):c.559C>G (p.Leu187Val)	CHAF1A, UBXN6 (L187V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345819	NM_025241.3(UBXN6):c.973A>G (p.Lys325Glu)	CHAF1A, UBXN6 (K272E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332027	NM_025241.3(UBXN6):c.881A>G (p.Asn294Ser)	UBXN6, CHAF1A (N241S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311089	NM_025241.3(UBXN6):c.1294G>A (p.Glu432Lys)	CHAF1A, UBXN6 (E379K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306974	NM_025241.3(UBXN6):c.619C>T (p.Arg207Cys)	CHAF1A, UBXN6 (R207C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303259	NM_025241.3(UBXN6):c.734C>G (p.Thr245Ser)	CHAF1A, UBXN6 (T192S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281201	NM_025241.3(UBXN6):c.946G>C (p.Val316Leu)	CHAF1A, UBXN6 (V263L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276493	NM_025241.3(UBXN6):c.953G>A (p.Arg318Gln)	CHAF1A, UBXN6 (R265Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263062	NM_025241.3(UBXN6):c.1262C>T (p.Ala421Val)	CHAF1A, UBXN6 (A421V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240401	NM_025241.3(UBXN6):c.769A>G (p.Lys257Glu)	CHAF1A, UBXN6 (K204E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233448	NM_025241.3(UBXN6):c.1270G>A (p.Glu424Lys)	CHAF1A, UBXN6 (E371K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 37