Product Details
- SNP ID
-
rs1805029
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:151839269 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTGAGAACTGGAAGACAAGCGGTT[C/T]CTACTCTTCCGAGCCCTTTCATTGT
- Phenotype
-
MIM: 601949
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CACNB4
PubMed Links
Gene Details
- Gene
- CACNB4
- Gene Name
- calcium voltage-gated channel auxiliary subunit beta 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
XM_011511795.2 |
2201 |
Silent Mutation |
AGA,AGG |
R424R |
XP_011510097.1 |
XM_011511796.2 |
2201 |
Silent Mutation |
AGA,AGG |
R423R |
XP_011510098.1 |
XM_011511797.2 |
2201 |
Silent Mutation |
AGA,AGG |
R408R |
XP_011510099.1 |
XM_011511798.2 |
2201 |
Intron |
|
|
XP_011510100.1 |
XM_017004880.1 |
2201 |
Silent Mutation |
AGA,AGG |
R390R |
XP_016860369.1 |
XM_017004881.1 |
2201 |
Silent Mutation |
AGA,AGG |
R374R |
XP_016860370.1 |
XM_017004882.1 |
2201 |
Silent Mutation |
AGA,AGG |
R361R |
XP_016860371.1 |
XM_017004883.1 |
2201 |
Silent Mutation |
AGA,AGG |
R285R |
XP_016860372.1 |
XM_017004884.1 |
2201 |
Silent Mutation |
AGA,AGG |
R253R |
XP_016860373.1 |
XM_017004885.1 |
2201 |
Silent Mutation |
AGA,AGG |
R253R |
XP_016860374.1 |
XM_017004886.1 |
2201 |
Silent Mutation |
AGA,AGG |
R232R |
XP_016860375.1 |
XM_017004887.1 |
2201 |
Intron |
|
|
XP_016860376.1 |
XM_017004888.1 |
2201 |
Intron |
|
|
XP_016860377.1 |
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