"Ambry Genetics"[submitter] AND "CDC25B"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2305093	NM_021873.4(CDC25B):c.10C>T (p.Pro4Ser)	CDC25B, LOC130065339 (P4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 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 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 3140813	NM_021873.4(CDC25B):c.484G>A (p.Val162Met)	CDC25B, LOC125384565 (V148M +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2561656	NM_021873.4(CDC25B):c.491G>A (p.Arg164Gln)	CDC25B, LOC125384565 (R100Q +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
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 2535266	NM_021873.4(CDC25B):c.778C>T (p.Pro260Ser)	CDC25B (P260S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140815	NM_021873.4(CDC25B):c.952C>T (p.Leu318Phe)	CDC25B, LOC126862955 (L206F +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597131	NM_021873.4(CDC25B):c.982G>A (p.Val328Met)	CDC25B, LOC126862955 (V314M +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391097	NM_021873.4(CDC25B):c.988C>T (p.Arg330Trp)	CDC25B, LOC126862955 (R138W +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368595	NM_021873.4(CDC25B):c.1001A>G (p.Lys334Arg)	CDC25B, LOC126862955 (K142R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140809	NM_021873.4(CDC25B):c.1034C>T (p.Pro345Leu)	CDC25B, LOC126862955 (P233L +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140810	NM_021873.4(CDC25B):c.1060G>A (p.Val354Met)	CDC25B, LOC126862955 (V201M +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140811	NM_021873.4(CDC25B):c.1160G>A (p.Ser387Asn)	CDC25B, LOC126862955 (S323N +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 (R456Q +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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 27