Product Details

SNP ID

rs79869087

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:138285729 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCTTCACCAGAAGGGCAATCTGC[C/T]CCCGCAGCTGCCGCTCCCCTTCCTG

Phenotype

MIM: 157680

Polymorphism

C/T, 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	1819	Missense Mutation	GAG,GGG	E462G	NP_001274511.1
NM_001287583.1	1819	Missense Mutation	GAG,GGG	E540G	NP_001274512.1
NM_001318098.1	1819	Missense Mutation	GAG,GGG	E479G	NP_001305027.1
NM_001790.4	1819	Missense Mutation	GAG,GGG	E462G	NP_001781.2
NM_022809.3	1819	Missense Mutation	GAG,GGG	E389G	NP_073720.1
XM_005272145.3	1819	Missense Mutation	GAG,GGG	E506G	XP_005272202.1
XM_006714739.3	1819	Missense Mutation	GAG,GGG	E464G	XP_006714802.1
XM_011543759.2	1819	Missense Mutation	GAG,GGG	E486G	XP_011542061.1
XM_011543760.2	1819	Missense Mutation	GAG,GGG	E485G	XP_011542062.1
XM_011543761.2	1819	Missense Mutation	GAG,GGG	E467G	XP_011542063.1
XM_011543762.1	1819	Missense Mutation	GAG,GGG	E389G	XP_011542064.1
XM_011543763.1	1819	Missense Mutation	GAG,GGG	E351G	XP_011542065.1
XM_011543764.1	1819	Missense Mutation	GAG,GGG	E300G	XP_011542066.1
XM_017010101.1	1819	Missense Mutation	GAG,GGG	E428G	XP_016865590.1

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