Product Details

SNP ID
rs5934782
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:10162979 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGGATTCTTCTGGATGATGTTCTGT[A/G]TAATTGAAAATGTTCATAATAAAAA
Phenotype
MIM: 302910
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CLCN4 PubMed Links

Gene Details

Gene
CLCN4
Gene Name
chloride voltage-gated channel 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256944.1 Intron NP_001243873.1
NM_001830.3 Intron NP_001821.2

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