Product Details

SNP ID
rs145317226
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:111644317 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATCTGTCCCTCCTGGATTTCCTGC[C/T]GGGTCTCGGCAGGCAGATGGTTGAT
Phenotype
MIM: 604986
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BRAP PubMed Links

Gene Details

Gene
BRAP
Gene Name
BRCA1 associated protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006768.4 1656 Missense Mutation NP_006759.3
XM_005253944.4 1656 Missense Mutation XP_005254001.1
XM_011538789.2 1656 Missense Mutation XP_011537091.1
XM_017019992.1 1656 Missense Mutation XP_016875481.1
XM_017019993.1 1656 Missense Mutation XP_016875482.1
XM_017019994.1 1656 Missense Mutation XP_016875483.1
XM_017019995.1 1656 Missense Mutation XP_016875484.1

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