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SNP ID

rs116945089

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:125006064 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTCCTCTGTTTATCTGGGTCCT[A/G]CTCTCCTACTTGCATAAGGACACCA

Phenotype

MIM: 615627

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

BRI3BP PubMed Links

Gene Details

Gene

BRI3BP

Gene Name

BRI3 binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080626.5		Intron			NP_542193.3
XM_011537940.2		Intron			XP_011536242.1

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