Related gene-specific medical variations for Gene (Select 994) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264951	NM_021873.4(CDC25B):c.1106G>A (p.Arg369His)	CDC25B, LOC126862955 (R216H +8 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 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 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 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 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 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 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 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 2305093	NM_021873.4(CDC25B):c.10C>T (p.Pro4Ser)	CDC25B, LOC130065339 (P4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance