Product Details

SNP ID
rs7795149
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:143729538 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAATGTGATTTGTCTGCCTTTGGGT[A/C]ATCCAGCCTTGGGTAGAGAAGGAAT
Phenotype
MIM: 616252
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
TCAF2 PubMed Links

Gene Details

Gene
TCAF2
Gene Name
TRPM8 channel associated factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130025.1 4343 Intron NP_001123497.1
NM_001130026.2 4343 UTR 3 NP_001123498.2
NM_173678.2 4343 Intron NP_775949.2
XM_006715927.3 4343 UTR 3 XP_006715990.1
XM_006715928.3 4343 Intron XP_006715991.1
XM_011516059.2 4343 Intron XP_011514361.1

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