Product Details

SNP ID

rs200050409

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:98439679 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCTGGTGGCTGCCCTGCCAGCCC[A/G]GCATCCTCCTCTTCCACTCCACACT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM169B PubMed Links

Gene Details

Gene

FAM169B

Gene Name

family with sequence similarity 169 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182562.2	781	Silent Mutation	GCC,GCT	A177A	NP_872368.2

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