Product Details

SNP ID
rs191551474
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:143876030 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTGGGCATCTTCTTGGAGACTTT[A/G]AAGAAACTCGTGTCCCCTTTGTTGT
Phenotype
MIM: 616251
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TCAF1 PubMed Links

Gene Details

Gene
TCAF1
Gene Name
TRPM8 channel associated factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206938.1 918 Silent Mutation NP_001193867.1
NM_001206941.1 918 Intron NP_001193870.1
NM_014719.2 918 Silent Mutation NP_055534.1
XM_005250074.3 918 Missense Mutation XP_005250131.1
XM_005250075.2 918 Missense Mutation XP_005250132.1
XM_005250076.3 918 Intron XP_005250133.1
XM_005250077.2 918 Missense Mutation XP_005250134.1
XM_006716191.2 918 Missense Mutation XP_006716254.1
XM_006716192.3 918 Missense Mutation XP_006716255.1
XM_017012833.1 918 Missense Mutation XP_016868322.1
XM_017012834.1 918 Missense Mutation XP_016868323.1
XM_017012835.1 918 Missense Mutation XP_016868324.1
XM_017012836.1 918 Missense Mutation XP_016868325.1

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