Product Details
- SNP ID
-
rs149240169
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:143876093 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGCCAGCCACACTGGTCACGAGGTT[C/G]CCAGGGAACGTGAACAGAACCCTTT
- Phenotype
-
MIM: 616251
- Polymorphism
- C/G, Transversion 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 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
NP_001193867.1 |
NM_001206941.1 |
855 |
Intron |
|
|
NP_001193870.1 |
NM_014719.2 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
NP_055534.1 |
XM_005250074.3 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_005250131.1 |
XM_005250075.2 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_005250132.1 |
XM_005250076.3 |
855 |
Intron |
|
|
XP_005250133.1 |
XM_005250077.2 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_005250134.1 |
XM_006716191.2 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_006716254.1 |
XM_006716192.3 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_006716255.1 |
XM_017012833.1 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_016868322.1 |
XM_017012834.1 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_016868323.1 |
XM_017012835.1 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_016868324.1 |
XM_017012836.1 |
855 |
Silent Mutation |
GGC,GGG |
G172G |
XP_016868325.1 |
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