Product Details

SNP ID
rs139296611
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:146455233 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTGATCCTAATATGCCGCCAAT[A/G]CCTCCTCCAGGAGGGATACCTCCAC
Phenotype
MIM: 605409
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TCERG1 PubMed Links

Gene Details

Gene
TCERG1
Gene Name
transcription elongation regulator 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040006.1 463 Missense Mutation ATA,ATG I79M NP_001035095.1
NM_006706.3 463 Missense Mutation ATA,ATG I79M NP_006697.2
XM_005268365.2 463 Missense Mutation ATA,ATG I79M XP_005268422.1
XM_017008977.1 463 Missense Mutation ATA,ATG I79M XP_016864466.1
XM_017008978.1 463 Missense Mutation ATA,ATG I79M XP_016864467.1
XM_017008979.1 463 Missense Mutation ATA,ATG I79M XP_016864468.1
XM_017008980.1 463 Missense Mutation ATA,ATG I79M XP_016864469.1
XM_017008981.1 463 Intron XP_016864470.1
XM_017008982.1 463 UTR 5 XP_016864471.1
XM_017008983.1 463 UTR 5 XP_016864472.1
XM_017008984.1 463 Missense Mutation ATA,ATG I79M XP_016864473.1
XM_017008985.1 463 Missense Mutation ATA,ATG I79M XP_016864474.1

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