Product Details

SNP ID
rs149666383
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:32076838 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCCGCCGCTTCATTGGGTCCATC[A/G]TGAAGGAGGTGATTGGGTCCTAGAG
Phenotype
Polymorphism
A/G, 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_001319677.1 845 Missense Mutation ATG,GTG M16V NP_001306606.1
NM_001319678.1 845 Intron NP_001306607.1
NM_001319679.1 845 Intron NP_001306608.1
NM_018056.3 845 Missense Mutation ATG,GTG M143V NP_060526.2
XM_005270988.2 845 Missense Mutation ATG,GTG M16V XP_005271045.1
XM_006710724.1 845 Missense Mutation ATG,GTG M143V XP_006710787.1
XM_006710725.3 845 Missense Mutation ATG,GTG M143V XP_006710788.1
XM_011541681.2 845 Missense Mutation ATG,GTG M143V XP_011539983.1
XM_011541683.1 845 Missense Mutation ATG,GTG M16V XP_011539985.1
XM_011541684.2 845 UTR 5 XP_011539986.1
XM_017001595.1 845 Missense Mutation ATG,GTG M28V XP_016857084.1

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