Product Details

SNP ID
rs201067534
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:35478327 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATACTTCTTAGCTGGCTTAAAGGA[C/T]GGAGGAGCATCAATACTGAAGTCTG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
INO80C PubMed Links

Gene Details

Gene
INO80C
Gene Name
INO80 complex subunit C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098817.1 627 Silent Mutation CCA,CCG P170P NP_001092287.1
NM_001308064.1 627 Silent Mutation CCA,CCG P79P NP_001294993.1
NM_194281.3 627 Silent Mutation CCA,CCG P134P NP_919257.2
XM_005258196.4 627 Silent Mutation CCA,CCG P79P XP_005258253.1
XM_005258197.4 627 Silent Mutation CCA,CCG P79P XP_005258254.1
XM_011525812.2 627 Silent Mutation CCA,CCG P108P XP_011524114.1
XM_017025549.1 627 Silent Mutation CCA,CCG P79P XP_016881038.1

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