Product Details

SNP ID

rs114259036

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:138286129 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACCTGTCCTCTTCACGCAGACAGC[A/G]GCACCTTTAGAGAGAACCCAGAGAT

Phenotype

MIM: 157680

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CDC25C PubMed Links

Gene Details

Gene

CDC25C

Gene Name

cell division cycle 25C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001287582.1	1599	Missense Mutation	CGC,TGC	R389C	NP_001274511.1
NM_001287583.1	1599	Missense Mutation	CGC,TGC	R467C	NP_001274512.1
NM_001318098.1	1599	Missense Mutation	CGC,TGC	R406C	NP_001305027.1
NM_001790.4	1599	Missense Mutation	CGC,TGC	R389C	NP_001781.2
NM_022809.3	1599	Missense Mutation	CGC,TGC	R316C	NP_073720.1
XM_005272145.3	1599	Missense Mutation	CGC,TGC	R433C	XP_005272202.1
XM_006714739.3	1599	Missense Mutation	CGC,TGC	R391C	XP_006714802.1
XM_011543759.2	1599	Missense Mutation	CGC,TGC	R413C	XP_011542061.1
XM_011543760.2	1599	Missense Mutation	CGC,TGC	R412C	XP_011542062.1
XM_011543761.2	1599	Missense Mutation	CGC,TGC	R394C	XP_011542063.1
XM_011543762.1	1599	Missense Mutation	CGC,TGC	R316C	XP_011542064.1
XM_011543763.1	1599	Missense Mutation	CGC,TGC	R278C	XP_011542065.1
XM_011543764.1	1599	Missense Mutation	CGC,TGC	R227C	XP_011542066.1
XM_017010101.1	1599	Missense Mutation	CGC,TGC	R355C	XP_016865590.1

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