Product Details

SNP ID

rs148350639

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:86424249 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAACTGGAGGCTTCTCTACAACA[G/T]GACCCAAAGGAGCATTGCAGGTCCT

Phenotype

MIM: 604003

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CLCA2 PubMed Links

Gene Details

Gene

CLCA2

Gene Name

chloride channel accessory 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006536.5	164	Missense Mutation	AGG,ATG	R1M	NP_006527.1
XM_011542448.2	164	Missense Mutation	AGG,ATG	R1M	XP_011540750.1

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