Product Details

SNP ID

rs11670041

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:35224990 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCAGGGCCTTCCTTGCCTCCCGCCA[A/C]TGGGCATCGTTCTCTCTCCACTGAG

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM187B PubMed Links

Gene Details

Gene

FAM187B

Gene Name

family with sequence similarity 187 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152481.1	990	Missense Mutation	CAG,CAT	Q315H	NP_689694.1

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