Product Details

SNP ID

rs5745796

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:118016864 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCACTCAAGCAGCAGGAGCAGCCC[A/G]CGGCGACCAAGATCAGGAACCTGCC

Phenotype

MIM: 600407

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RFC5 PubMed Links

Gene Details

Gene

RFC5

Gene Name

replication factor C subunit 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130112.2	162	UTR 5			NP_001123584.1
NM_001206801.1	162	Missense Mutation	ACG,GCG	T13A	NP_001193730.1
NM_007370.5	162	Missense Mutation	ACG,GCG	T13A	NP_031396.1
NM_181578.3	162	UTR 5			NP_853556.2
XM_011538643.2	162	Missense Mutation	ACG,GCG	T13A	XP_011536945.1
XM_011538645.2	162	Missense Mutation	ACG,GCG	T13A	XP_011536947.1
XM_017019779.1	162	Missense Mutation	ACG,GCG	T13A	XP_016875268.1

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