Product Details

SNP ID
rs12368262
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:21802026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATCTAACTGTTTCATAAGGCTCT[C/G]TGATACCTTAGAGGAGCATTCACCT
Phenotype
MIM: 601439
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
ABCC9 PubMed Links

Gene Details

Gene
ABCC9
Gene Name
ATP binding cassette subfamily C member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005691.3 Intron NP_005682.2
NM_020297.3 Intron NP_064693.2
XM_005253284.3 Intron XP_005253341.1
XM_005253286.3 Intron XP_005253343.1
XM_005253287.4 Intron XP_005253344.1
XM_005253288.3 Intron XP_005253345.1
XM_005253289.3 Intron XP_005253346.1
XM_005253290.3 Intron XP_005253347.1
XM_006719025.3 Intron XP_006719088.1
XM_011520545.2 Intron XP_011518847.1

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