Product Details

SNP ID

rs146489542

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:40706187 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTATTTTTCCCAGGCTGAGGCAG[C/T]TAAATTAGTTCCAATGGGTTTCACC

Phenotype

MIM: 179617

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RAD51 PubMed Links

Gene Details

Gene

RAD51

Gene Name

RAD51 recombinase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164269.1	285	Intron			NP_001157741.1
NM_001164270.1	285	Missense Mutation	GCT,GTT	A79V	NP_001157742.1
NM_002875.4	285	Missense Mutation	GCT,GTT	A79V	NP_002866.2
NM_133487.3	285	Intron			NP_597994.3
XM_006720626.3	285	Missense Mutation	GCT,GTT	A79V	XP_006720689.1
XM_011521857.2	285	Missense Mutation	GCT,GTT	A79V	XP_011520159.1
XM_011521858.2	285	Missense Mutation	GCT,GTT	A79V	XP_011520160.1
XM_011521859.2	285	Missense Mutation	GCT,GTT	A79V	XP_011520161.1
XM_011521860.2	285	Missense Mutation	GCT,GTT	A79V	XP_011520162.1
XM_011521861.2	285	Missense Mutation	GCT,GTT	A79V	XP_011520163.1
XM_011521862.2	285	Intron			XP_011520164.1

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