Product Details

SNP ID
rs12476337
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:206000140 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACTGGAGAGTTCTGTTGACCATTTA[A/G]AAGACCATAATATTAGATTTCTATA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
INO80D PubMed Links

Gene Details

Gene
INO80D
Gene Name
INO80 complex subunit D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017759.4 7717 UTR 3 NP_060229.3
XM_011511369.2 7717 UTR 3 XP_011509671.1
XM_011511370.2 7717 Intron XP_011509672.1
XM_011511371.2 7717 Intron XP_011509673.1
XM_011511373.2 7717 Intron XP_011509675.1
XM_011511375.2 7717 UTR 3 XP_011509677.1
XM_011511376.2 7717 UTR 3 XP_011509678.1

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