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SNP ID

rs76711372

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:108570864 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATGGAACAGTTGGAGGATGAAGGC[C/T]TTAGTGATGTTAAAGGAAGATATGT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM102B PubMed Links

Gene Details

Gene

FAM102B

Gene Name

family with sequence similarity 102 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010883.2		Intron			NP_001010883.2

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