CDC25B[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380647	NM_021873.4(CDC25B):c.187G>A (p.Ala63Thr)	CDC25B (A63T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271887	NM_021873.4(CDC25B):c.187G>T (p.Ala63Ser)	CDC25B (A63S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264956	NM_021873.4(CDC25B):c.232C>T (p.Leu78Phe)	CDC25B (L14F +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2243202	NM_021873.4(CDC25B):c.355A>G (p.Met119Val)	CDC25B (M41V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2597452	NM_021873.4(CDC25B):c.367A>G (p.Met123Val)	CDC25B (M109V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264952	NM_021873.4(CDC25B):c.424G>A (p.Glu142Lys)	CDC25B (E142K +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2230254	NM_021873.4(CDC25B):c.443G>A (p.Arg148His)	CDC25B (R134H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2652190	NM_021873.4(CDC25B):c.516C>T (p.Pro172=)	CDC25B	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2311741	NM_021873.4(CDC25B):c.520G>A (p.Gly174Ser)	CDC25B (G174S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2459756	NM_021873.4(CDC25B):c.587G>C (p.Gly196Ala)	CDC25B (G43A +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287708	NM_021873.4(CDC25B):c.712A>G (p.Ser238Gly)	CDC25B (S197G +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336758	NM_021873.4(CDC25B):c.745A>C (p.Ser249Arg)	CDC25B (S171R +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515807	NM_021873.4(CDC25B):c.761G>A (p.Gly254Asp)	CDC25B (G62D +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264949	NM_021873.4(CDC25B):c.763C>T (p.Arg255Cys)	CDC25B (R191C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535266	NM_021873.4(CDC25B):c.778C>T (p.Pro260Ser)	CDC25B (P68S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264953	NM_021873.4(CDC25B):c.835T>G (p.Leu279Val)	CDC25B (L126V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264950	NM_021873.4(CDC25B):c.1410C>G (p.Ser470Arg)	CDC25B (S278R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264955	NM_021873.4(CDC25B):c.1444A>G (p.Ile482Val)	CDC25B (I329V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140812	NM_021873.4(CDC25B):c.1510C>G (p.Arg504Gly)	CDC25B (R463G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296632	NM_021873.4(CDC25B):c.1528G>A (p.Asp510Asn)	CDC25B (D318N +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385960	NM_021873.4(CDC25B):c.1702C>T (p.Arg568Trp)	CDC25B (R376W +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392738	NM_021873.4(CDC25B):c.1703G>A (p.Arg568Gln)	CDC25B (R477Q +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230447	NM_021873.4(CDC25B):c.1709G>A (p.Arg570Gln)	CDC25B (R417Q +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223107	NM_021873.4(CDC25B):c.1711C>T (p.Arg571Trp)	CDC25B (R493W +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24