Search

  • Order Status
  • Quick Order
  • Promos

System Message

OKCancel
LOADING ...
See other BRCA1 GT Assays ›
SNP ID:
rs1799966
Gene
BRCA1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.17: 43071077 - 43071077 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TCAGTAGTATGAGCAGCAGCTGGAC[C/T]CTGGGCAGATTCTGCAACTTTCAAT

Assay ID C___2615208_20
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
Check your price ›

Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 113705

Literature Links:

 BRCA1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.36)
(0.64)
Caucasian - Not Available CEPH (CEU)
G (0.31)
(0.69)
EAS
G (0.37)
(0.63)
African American - Not Available YRI (Yoruba)
G (0.17)
(0.83)
SAS
G (0.50)
(0.50)
Chinese - Not Available JPT (Japanese)
G (0.27)
(0.73)
AFR
G (0.23)
(0.77)
Japanese - Not Available CHB (Han Chinese)
G (0.31)
(0.69)
EUR
G (0.36)
(0.64)
AMR
G (0.38)
(0.62)
BRCA1 - BRCA1, DNA repair associated
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_007294.3 5132 Missense Mutation NP_009225.1
NM_007297.3 5132 Missense Mutation NP_009228.2
NM_007298.3 5132 Missense Mutation NP_009229.2
NM_007299.3 5132 Missense Mutation NP_009230.2
NM_007300.3 5132 Missense Mutation NP_009231.2

Back To Top

More Information


Set Membership:

 HapMap

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products