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SNP ID

rs149008261

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:30778448 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCCTCAGGGCTTAAAGAAGACAT[A/G]TGTGACCATGGACCAGGAACGCCCA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM188B PubMed Links

Gene Details

Gene

FAM188B

Gene Name

family with sequence similarity 188 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032222.2	157	Missense Mutation	TAT,TGT	Y27C	NP_115598.2

Gene

INMT-FAM188B

Gene Name

INMT-FAM188B readthrough (NMD candidate)

There are no transcripts associated with this gene.

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