Product Details

SNP ID

rs11200996

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:84334195 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAACAGTTGTGGTTGGTGTGCCCT[G/T]CTGTCATAAGCTGATTGTGGTTGTA

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CCSER2 PubMed Links

Additional Information

For this assay, SNP(s) [rs114826685] 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

CCSER2

Gene Name

coiled-coil serine rich protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284240.1		Intron			NP_001271169.1
NM_001284241.1		Intron			NP_001271170.1
NM_001284242.1		Intron			NP_001271171.1
NM_001284243.1		Intron			NP_001271172.1
NM_018999.3		Intron			NP_061872.2
XM_005269905.3		Intron			XP_005269962.1
XM_005269906.3		Intron			XP_005269963.1
XM_005269908.3		Intron			XP_005269965.1
XM_006717894.1		Intron			XP_006717957.1
XM_006717895.1		Intron			XP_006717958.1
XM_011539870.2		Intron			XP_011538172.1
XM_011539871.2		Intron			XP_011538173.1
XM_011539872.2		Intron			XP_011538174.1
XM_011539873.1		Intron			XP_011538175.1
XM_017016340.1		Intron			XP_016871829.1
XM_017016341.1		Intron			XP_016871830.1
XM_017016342.1		Intron			XP_016871831.1
XM_017016343.1		Intron			XP_016871832.1

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