Product Details

SNP ID
rs145394914
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:2717824 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAATGAGGGCAGCCAACACCGCAGG[A/G]GCATTTGCTCCCTGGGTGCCCGTTC
Phenotype
MIM: 607604
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
KCNV2 PubMed Links

Gene Details

Gene
KCNV2
Gene Name
potassium voltage-gated channel modifier subfamily V member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_133497.3 299 Missense Mutation AGC,GGC S29G NP_598004.1

View Full Product Details