Product Details

SNP ID
rs7910506
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:18518128 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAGCATTTCTTGAGATGAGCAAGAA[A/G]ACTGTAGACAACAGTAACTTGAAAC
Phenotype
MIM: 600003
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CACNB2 PubMed Links

Gene Details

Gene
CACNB2
Gene Name
calcium voltage-gated channel auxiliary subunit beta 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000724.3 Intron NP_000715.2
NM_001167945.1 Intron NP_001161417.1
NM_201570.2 Intron NP_963864.1
NM_201571.3 Intron NP_963865.2
NM_201572.3 Intron NP_963866.2
NM_201590.2 Intron NP_963884.2
NM_201593.2 Intron NP_963887.2
NM_201596.2 Intron NP_963890.2
NM_201597.2 Intron NP_963891.1
XM_005252588.3 Intron XP_005252645.1
XM_005252591.3 Intron XP_005252648.1
XM_006717502.3 Intron XP_006717565.1
XM_011519659.2 Intron XP_011517961.1
XM_011519660.2 Intron XP_011517962.1
XM_017016625.1 Intron XP_016872114.1
Gene
NSUN6
Gene Name
NOP2/Sun RNA methyltransferase family member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182543.3 Intron NP_872349.1
XM_011519383.1 Intron XP_011517685.1
XM_011519384.1 Intron XP_011517686.1
XM_011519385.1 Intron XP_011517687.1
XM_011519386.2 Intron XP_011517688.1
XM_011519387.2 Intron XP_011517689.1
XM_011519389.2 Intron XP_011517691.1
XM_017015906.1 Intron XP_016871395.1
XM_017015907.1 Intron XP_016871396.1
XM_017015908.1 Intron XP_016871397.1
XM_017015909.1 Intron XP_016871398.1
XM_017015910.1 Intron XP_016871399.1
XM_017015911.1 Intron XP_016871400.1
XM_017015912.1 Intron XP_016871401.1
XM_017015913.1 Intron XP_016871402.1
XM_017015914.1 Intron XP_016871403.1

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