Product Details

SNP ID

rs17005658

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:140266676 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATATTAGTGGTAAAGGTGTTAGAGT[C/T]TAGACTGACAAAATCAAGACAAAAT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SCOC PubMed Links

Additional Information

For this assay, SNP(s) [rs77524101] 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

SCOC

Gene Name

short coiled-coil protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001153446.1		Intron			NP_001146918.1
NM_001153484.1		Intron			NP_001146956.1
NM_001153552.1		Intron			NP_001147024.1
NM_001153585.1		Intron			NP_001147057.1
NM_001153635.1		Intron			NP_001147107.1
NM_001153663.1		Intron			NP_001147135.1
NM_001153690.1		Intron			NP_001147162.1
NM_032547.2		Intron			NP_115936.2

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