Related gene-specific medical variations for Gene (Select 157313) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141005	NM_152562.4(CDCA2):c.955C>T (p.Leu319Phe)	CDCA2, LOC126860331 (L319F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141000	NM_152562.4(CDCA2):c.3020G>A (p.Ser1007Asn)	CDCA2, LOC124153127 (S1007N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2658494	NM_152562.4(CDCA2):c.954C>T (p.Asp318=)	CDCA2, LOC126860331	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2615756	NM_152562.4(CDCA2):c.3038A>G (p.Glu1013Gly)	CDCA2, LOC124153127 (E1013G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590987	NM_152562.4(CDCA2):c.2860G>A (p.Val954Ile)	CDCA2, LOC124153127 (V939I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471978	NM_152562.4(CDCA2):c.2987G>A (p.Arg996Gln)	CDCA2, LOC124153127 (R981Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407287	NM_152562.4(CDCA2):c.959C>T (p.Pro320Leu)	CDCA2, LOC126860331 (P305L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372933	NM_152562.4(CDCA2):c.827A>G (p.Lys276Arg)	CDCA2, LOC126860331 (K261R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349450	NM_152562.4(CDCA2):c.851A>G (p.Lys284Arg)	CDCA2, LOC126860331 (K269R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346995	NM_152562.4(CDCA2):c.2905G>T (p.Asp969Tyr)	CDCA2, LOC124153127 (D969Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346394	NM_152562.4(CDCA2):c.983G>A (p.Arg328His)	CDCA2, LOC126860331 (R328H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334709	NM_152562.4(CDCA2):c.3018G>C (p.Glu1006Asp)	CDCA2, LOC124153127 (E1006D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314549	NM_152562.4(CDCA2):c.829G>T (p.Val277Phe)	CDCA2, LOC126860331 (V277F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255416	NM_152562.4(CDCA2):c.1003T>C (p.Ser335Pro)	CDCA2, LOC126860331 (S335P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220500	NM_152562.4(CDCA2):c.835G>T (p.Asp279Tyr)	CDCA2, LOC126860331 (D279Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768231	NM_152562.4(CDCA2):c.873G>A (p.Ser291=)	CDCA2, LOC126860331	Single nucleotide variant (synonymous variant)	not provided	GBenign