Product Details

SNP ID

rs648248

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:116759894 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGTTCTTTCCTTCCCCCGGTCTTC[C/T]CATGGCTAGCTTATTCTCATCCTCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM162B PubMed Links

Gene Details

Gene

FAM162B

Gene Name

family with sequence similarity 162 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085480.2		Intron			NP_001078949.1

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