Product Details

SNP ID

rs2275252

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:43880238 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATGAACCTCAGAGGGAGCCCCGAG[A/C]GATGGGGAGCAAAGGTTAGGGGAAG

Phenotype

MIM: 613408 MIM: 613409

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

CCDC122 PubMed Links

Additional Information

For this assay, SNP(s) [rs74764587] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CCDC122

Gene Name

coiled-coil domain containing 122

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144974.3	330	Intron			NP_659411.2
XM_017020397.1	330	Intron			XP_016875886.1
XM_017020398.1	330	Intron			XP_016875887.1
XM_017020399.1	330	Intron			XP_016875888.1

Gene

LACC1

Gene Name

laccase domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128303.1	330	Intron			NP_001121775.1
NM_153218.2	330	Intron			NP_694950.2
XM_005266261.3	330	Intron			XP_005266318.1
XM_006719766.3	330	Intron			XP_006719829.1
XM_006719767.3	330	Intron			XP_006719830.1
XM_011534933.2	330	Intron			XP_011533235.1
XM_011534934.2	330	Intron			XP_011533236.1
XM_011534935.2	330	Intron			XP_011533237.1
XM_017020394.1	330	UTR 5			XP_016875883.1

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