Product Details
- SNP ID
-
rs55889089
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:74728314 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGTTTCTAATTGCATCTTCCCCCA[A/G]ATTGGCCGGTCCAAACACCATTCCT
- Phenotype
-
MIM: 607009
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TRPM6
PubMed Links
Gene Details
- Gene
- TRPM6
- Gene Name
- transient receptor potential cation channel subfamily M member 6
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001177310.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1949L |
NP_001170781.1 |
NM_001177311.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1949L |
NP_001170782.1 |
NM_017662.4 |
5822 |
Silent Mutation |
CTG,TTG |
L1954L |
NP_060132.3 |
XM_011518244.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1953L |
XP_011516546.1 |
XM_011518245.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1923L |
XP_011516547.1 |
XM_011518246.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1913L |
XP_011516548.1 |
XM_011518247.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1911L |
XP_011516549.1 |
XM_011518248.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1907L |
XP_011516550.1 |
XM_011518249.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1876L |
XP_011516551.1 |
XM_011518250.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1862L |
XP_011516552.1 |
XM_011518251.2 |
5822 |
Silent Mutation |
CTG,TTG |
L1711L |
XP_011516553.1 |
XM_011518252.2 |
5822 |
Intron |
|
|
XP_011516554.1 |
XM_011518255.2 |
5822 |
Intron |
|
|
XP_011516557.1 |
XM_017014287.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1833L |
XP_016869776.1 |
XM_017014288.1 |
5822 |
Silent Mutation |
CTG,TTG |
L1784L |
XP_016869777.1 |
XM_017014289.1 |
5822 |
Intron |
|
|
XP_016869778.1 |
View Full Product Details