Product Details

SNP ID

rs8069166

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:443347 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCGGGTGGGCCTGTGGCGTGGCTC[A/G]AAGCGCACCTCGGCCTTGTAGTTGC

Phenotype

MIM: 615928

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM101B PubMed Links

Gene Details

Gene

FAM101B

Gene Name

family with sequence similarity 101 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182705.2	526	Silent Mutation	TTC,TTT	F154F	NP_874364.1

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