Product Details
- SNP ID
-
rs112440901
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:16417683 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCTCCTAGGATGACCTCACCCTC[C/T]AGCTCTCCAGTTTTCAGGTTGGAGA
- Phenotype
-
MIM: 606676
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TRPV2
PubMed Links
Gene Details
- Gene
- TRPV2
- Gene Name
- transient receptor potential cation channel subfamily V member 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_016113.4 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
NP_057197.2 |
| XM_005256676.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_005256733.1 |
| XM_005256677.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_005256734.1 |
| XM_005256678.4 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_005256735.1 |
| XM_006721541.3 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_006721604.1 |
| XM_006721543.3 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_006721606.1 |
| XM_011523922.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_011522224.1 |
| XM_011523923.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_011522225.1 |
| XM_011523925.2 |
414 |
Intron |
|
|
XP_011522227.1 |
| XM_017024730.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_016880219.1 |
| XM_017024731.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_016880220.1 |
| XM_017024732.1 |
414 |
Silent Mutation |
TCC,TCT |
S5S |
XP_016880221.1 |
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