Product Details

SNP ID
rs1065358
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:44220153 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGTGCCACACGCGGGTCTCCTCA[A/G]ACTGGCTGGTGCGGGGCCGGCCCTG
Phenotype
MIM: 607707 MIM: 606209
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CAMK2B PubMed Links
Additional Information
For this assay, SNP(s) [rs77158048] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
CAMK2B
Gene Name
calcium/calmodulin dependent protein kinase II beta
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001220.4 2125 Missense Mutation TCT,TTT S637F NP_001211.3
NM_001293170.1 2125 Missense Mutation TCT,TTT S513F NP_001280099.1
NM_172078.2 2125 Missense Mutation TCT,TTT S513F NP_742075.1
NM_172079.2 2125 Missense Mutation TCT,TTT S489F NP_742076.1
NM_172080.2 2125 Missense Mutation TCT,TTT S488F NP_742077.1
NM_172081.2 2125 Missense Mutation TCT,TTT S474F NP_742078.1
NM_172082.2 2125 Missense Mutation TCT,TTT S463F NP_742079.1
NM_172083.2 2125 Missense Mutation TCT,TTT S450F NP_742080.1
NM_172084.2 2125 Missense Mutation TCT,TTT S420F NP_742081.1
XM_005249862.3 2125 Missense Mutation TCT,TTT S498F XP_005249919.1
XM_005249864.3 2125 Missense Mutation TCT,TTT S465F XP_005249921.1
XM_006715781.2 2125 Missense Mutation TCT,TTT S597F XP_006715844.1
XM_006715784.2 2125 Missense Mutation TCT,TTT S489F XP_006715847.1
XM_011515547.1 2125 Missense Mutation TCT,TTT S680F XP_011513849.1
XM_011515549.1 2125 Missense Mutation TCT,TTT S665F XP_011513851.1
XM_011515550.1 2125 Missense Mutation TCT,TTT S656F XP_011513852.1
XM_011515551.1 2125 Missense Mutation TCT,TTT S656F XP_011513853.1
XM_011515552.1 2125 Missense Mutation TCT,TTT S655F XP_011513854.1
XM_011515553.1 2125 Missense Mutation TCT,TTT S642F XP_011513855.1
XM_011515554.1 2125 Missense Mutation TCT,TTT S640F XP_011513856.1
XM_011515555.1 2125 Missense Mutation TCT,TTT S637F XP_011513857.1
XM_011515556.1 2125 Missense Mutation TCT,TTT S632F XP_011513858.1
XM_011515557.1 2125 Missense Mutation TCT,TTT S631F XP_011513859.1
XM_011515558.2 2125 Intron XP_011513860.1
XM_011515559.1 2125 Missense Mutation TCT,TTT S551F XP_011513861.1
XM_017012660.1 2125 Missense Mutation TCT,TTT S641F XP_016868149.1
XM_017012661.1 2125 Missense Mutation TCT,TTT S627F XP_016868150.1
XM_017012662.1 2125 Missense Mutation TCT,TTT S574F XP_016868151.1
XM_017012663.1 2125 Missense Mutation TCT,TTT S527F XP_016868152.1
XM_017012664.1 2125 Missense Mutation TCT,TTT S473F XP_016868153.1
XM_017012665.1 2125 Missense Mutation TCT,TTT S464F XP_016868154.1
XM_017012666.1 2125 Missense Mutation TCT,TTT S384F XP_016868155.1
XM_017012667.1 2125 Missense Mutation TCT,TTT S369F XP_016868156.1
XM_017012668.1 2125 Missense Mutation TCT,TTT S360F XP_016868157.1
XM_017012669.1 2125 Missense Mutation TCT,TTT S360F XP_016868158.1
XM_017012670.1 2125 Missense Mutation TCT,TTT S345F XP_016868159.1
Gene
YKT6
Gene Name
YKT6 v-SNARE homolog (S. cerevisiae)
There are no transcripts associated with this gene.

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