Product Details

SNP ID

rs61756141

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:104126891 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTATTTTATTATGTCAAAGTTCACC[A/G]TCCTAAAAACAAAAACAGATAATAT

Phenotype

MIM: 602331

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ORC5 PubMed Links

Gene Details

Gene

ORC5

Gene Name

origin recognition complex subunit 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002553.3	1408	Missense Mutation	ACG,ATG	T422M	NP_002544.1
NM_181747.3	1408	Intron			NP_859531.1
XM_011516273.2	1408	Intron			XP_011514575.1

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