Product Details

SNP ID

rs185467446

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:13170951 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAGACAATCTGTCTCTGCTGACC[C/G]CACTGCTGGAAGAAAATGAGTCAGC

Phenotype

MIM: 609357

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MCM10 PubMed Links

Gene Details

Gene

MCM10

Gene Name

minichromosome maintenance 10 replication initiation factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018518.4	165	Missense Mutation	CCA,GCA	P13A	NP_060988.3
NM_182751.2	165	Missense Mutation	CCA,GCA	P13A	NP_877428.1
XM_011519538.2	165	Missense Mutation	CCA,GCA	P13A	XP_011517840.1

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