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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