Product Details

SNP ID
rs150765440
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:99784651 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTCCGGAGGCAGACCTGCCACTTT[A/G]TTTTGAGCAAACTGTTCTGGTGTGG
Phenotype
MIM: 601107
Polymorphism
A/G, Transition 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_000392.4 301 Missense Mutation TAT,TGT Y26C NP_000383.1
XM_006717630.3 301 Intron XP_006717693.1
XM_006717631.3 301 Missense Mutation TAT,TGT Y26C XP_006717694.1
XM_011539291.2 301 Missense Mutation TAT,TGT Y26C XP_011537593.1
XM_017015675.1 301 Missense Mutation TAT,TGT Y26C XP_016871164.1

View Full Product Details