Product Details

SNP ID
rs12089746
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:32076626 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGTAGGTAATTTCCTGGCCTGA[C/T]TCAGCTGGAGGCCGATGAAGGTCAG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM39B PubMed Links

Gene Details

Gene
TMEM39B
Gene Name
transmembrane protein 39B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319677.1 226 Intron NP_001306606.1
NM_001319678.1 226 Intron NP_001306607.1
NM_001319679.1 226 Intron NP_001306608.1
NM_018056.3 226 Intron NP_060526.2
XM_005270988.2 226 Intron XP_005271045.1
XM_006710724.1 226 Intron XP_006710787.1
XM_006710725.3 226 Intron XP_006710788.1
XM_011541681.2 226 Intron XP_011539983.1
XM_011541683.1 226 Intron XP_011539985.1
XM_011541684.2 226 Intron XP_011539986.1
XM_017001595.1 226 UTR 5 XP_016857084.1

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