Product Details

SNP ID

rs11975856

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:12572007 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTGTTTGTTTAGTTTTATCCCTGA[A/G]CTTAGGAGGAAAACACACAAAACCA

Phenotype

MIM: 613416

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SCIN PubMed Links

Additional Information

For this assay, SNP(s) [rs74569342] are located under a probe 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

SCIN

Gene Name

scinderin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001112706.2		Intron			NP_001106177.1
NM_033128.3		Intron			NP_149119.1

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