Product Details

SNP ID

rs190100022

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:56359011 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCGCCTAGCTGCGCACCATGGC[C/T]GGGTTGCTGGCGTTGCTGGGTCCGG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM210B PubMed Links

Gene Details

Gene

FAM210B

Gene Name

family with sequence similarity 210 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080821.2	85	Silent Mutation	GCC,GCT	A2A	NP_543011.2

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