Product Details

SNP ID

rs115096265

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:154745317 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAATATTGTATTCCTCTCAGCACAC[C/T]ATATCAGGAATCATGTTGTCCACAT

Phenotype

MIM: 616024

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SCAF8 PubMed Links

Additional Information

For this assay, SNP(s) [rs200626503] 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

SCAF8

Gene Name

SR-related CTD associated factor 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286188.1		Intron			NP_001273117.1
NM_001286189.1		Intron			NP_001273118.1
NM_001286194.1		Intron			NP_001273123.1
NM_001286199.1		Intron			NP_001273128.1
NM_014892.4		Intron			NP_055707.3

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