Product Details

SNP ID

rs186026858

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:86560338 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGACCTTCTACTTGGAAAAAAAC[A/G]AAATGAATATGGACCACCAGGTAGA

Phenotype

MIM: 616857

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLCA4 PubMed Links

Gene Details

Gene

CLCA4

Gene Name

chloride channel accessory 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012128.3	472	Missense Mutation	CAA,CGA	Q143R	NP_036260.2
XM_011541015.2	472	Missense Mutation	CAA,CGA	Q92R	XP_011539317.1

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