Product Details

SNP ID

rs78445627

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:116752339 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTGAAGTGTTGCCAATATTCTAC[A/G]TCTTCACTTTGGCAGTGGTTACACA

Phenotype

Polymorphism

A/G, 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	894	UTR 3			NP_001078949.1

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