Product Details

SNP ID

rs201840590

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:86560334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCCTGACCTTCTACTTGGAAAA[A/C]AACAAAATGAATATGGACCACCAGG

Phenotype

MIM: 616857

Polymorphism

A/C, Transversion 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	468	Missense Mutation	AAA,CAA	K142Q	NP_036260.2
XM_011541015.2	468	Missense Mutation	AAA,CAA	K91Q	XP_011539317.1

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