Product Details

SNP ID
rs76306962
Assay Type
Functionally Tested
NCBI dbSNP Submissions
3
Location
Chr.1:190098586 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATAAACCAGCTCTCAGAGTGGCTG[C/G]CTCCGAAGGGATTGACATAAACAGC
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
BRINP3 PubMed Links

Gene Details

Gene
BRINP3
Gene Name
BMP/retinoic acid inducible neural specific 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317188.1 2308 Missense Mutation GCC,GGC A476G NP_001304117.1
NM_199051.2 2308 Missense Mutation GCC,GGC A578G NP_950252.1
XM_011509472.2 2308 Missense Mutation GCC,GGC A548G XP_011507774.1
XM_011509475.2 2308 Missense Mutation GCC,GGC A535G XP_011507777.1
XM_011509476.2 2308 Missense Mutation GCC,GGC A476G XP_011507778.1
XM_017001125.1 2308 Missense Mutation GCC,GGC A578G XP_016856614.1
XM_017001126.1 2308 Missense Mutation GCC,GGC A578G XP_016856615.1
XM_017001127.1 2308 Missense Mutation GCC,GGC A548G XP_016856616.1
XM_017001128.1 2308 Missense Mutation GCC,GGC A548G XP_016856617.1
XM_017001129.1 2308 Missense Mutation GCC,GGC A476G XP_016856618.1
XM_017001130.1 2308 Missense Mutation GCC,GGC A476G XP_016856619.1
XM_017001131.1 2308 Missense Mutation GCC,GGC A285G XP_016856620.1
XM_017001132.1 2308 Intron XP_016856621.1
XM_017001133.1 2308 Intron XP_016856622.1

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