CDCA7L[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2279245	NM_018719.5(CDCA7L):c.1351G>T (p.Val451Leu)	CDCA7L (V405L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229418	NM_018719.5(CDCA7L):c.1225A>G (p.Ile409Val)	CDCA7L (I363V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552151	NM_018719.5(CDCA7L):c.1159C>T (p.Arg387Cys)	CDCA7L (R353C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141028	NM_018719.5(CDCA7L):c.1081A>G (p.Ile361Val)	CDCA7L (I315V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322019	NM_018719.5(CDCA7L):c.1022G>A (p.Arg341Gln)	CDCA7L (R307Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141034	NM_018719.5(CDCA7L):c.980A>G (p.Asp327Gly)	CDCA7L (D281G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141033	NM_018719.5(CDCA7L):c.946C>T (p.Arg316Cys)	CDCA7L (R270C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289254	NM_018719.5(CDCA7L):c.932G>A (p.Arg311Gln)	CDCA7L (R265Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2525995	NM_018719.5(CDCA7L):c.902G>A (p.Arg301Gln)	CDCA7L (R255Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517326	NM_018719.5(CDCA7L):c.880G>C (p.Ala294Pro)	CDCA7L (A260P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141032	NM_018719.5(CDCA7L):c.775G>A (p.Ala259Thr)	CDCA7L (A213T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791284	NM_018719.5(CDCA7L):c.682-9G>C	CDCA7L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2555325	NM_018719.5(CDCA7L):c.656T>C (p.Met219Thr)	CDCA7L (M185T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560068	NM_018719.5(CDCA7L):c.629G>C (p.Ser210Thr)	CDCA7L (S164T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141030	NM_018719.5(CDCA7L):c.610C>T (p.Arg204Trp)	CDCA7L (R204W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553888	NM_018719.5(CDCA7L):c.539T>C (p.Leu180Pro)	CDCA7L (L146P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517736	NM_018719.5(CDCA7L):c.512G>A (p.Arg171His)	CDCA7L (R137H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2300374	NM_018719.5(CDCA7L):c.469C>T (p.Pro157Ser)	CDCA7L (P123S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2206127	NM_018719.5(CDCA7L):c.457C>G (p.Leu153Val)	CDCA7L (L119V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141029	NM_018719.5(CDCA7L):c.428G>A (p.Arg143Gln)	CDCA7L (R143Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211170	NM_018719.5(CDCA7L):c.364G>C (p.Asp122His)	CDCA7L (D76H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554252	NM_018719.5(CDCA7L):c.352G>A (p.Glu118Lys)	CDCA7L (E118K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484045	NM_018719.5(CDCA7L):c.322A>T (p.Ser108Cys)	CDCA7L (S74C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277349	NM_018719.5(CDCA7L):c.263C>T (p.Thr88Met)	CDCA7L (T54M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378703	NM_018719.5(CDCA7L):c.185C>G (p.Ser62Cys)	CDCA7L (S62C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141027	NM_018719.5(CDCA7L):c.100C>T (p.Pro34Ser)	CDCA7L (P34S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 26