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SNP ID

rs6592081

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:82732630 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGGCGAAAGAGGCCAAATGGCCC[C/G]GCCCGTCCTCCCCGCCGGGAGAATC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM181B PubMed Links

Gene Details

Gene

FAM181B

Gene Name

family with sequence similarity 181 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175885.3	1235	Missense Mutation	CCG,CGG	P367R	NP_787081.2

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