Product Details

SNP ID
rs145427140
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:99784780 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCACCAAACTCTATCTTGCTAAGC[A/C]GGTAAAGTTAACACCACTGTTTCTG
Phenotype
MIM: 601107
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ABCC2 PubMed Links

Gene Details

Gene
ABCC2
Gene Name
ATP binding cassette subfamily C member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000392.4 430 Missense Mutation CAG,CCG Q69P NP_000383.1
XM_006717630.3 430 Intron XP_006717693.1
XM_006717631.3 430 Missense Mutation CAG,CCG Q69P XP_006717694.1
XM_011539291.2 430 Missense Mutation CAG,CCG Q69P XP_011537593.1
XM_017015675.1 430 Missense Mutation CAG,CCG Q69P XP_016871164.1

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