Product Details

SNP ID
rs199876915
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:36200381 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCGAGGGCCGGCGTTCCCCGTCCC[C/T]CTACAGTCTCAAGTGCTCACCCACC
Phenotype
MIM: 616856
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BRPF3 PubMed Links

Gene Details

Gene
BRPF3
Gene Name
bromodomain and PHD finger containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015695.2 289 Missense Mutation CCC,CTC P20L NP_056510.2
XM_005249010.2 289 Missense Mutation CCC,CTC P20L XP_005249067.1
XM_005249011.3 289 Missense Mutation CCC,CTC P20L XP_005249068.1
XM_011514489.1 289 Missense Mutation CCC,CTC P20L XP_011512791.1
XM_011514490.1 289 Missense Mutation CCC,CTC P20L XP_011512792.1
XM_011514491.1 289 Missense Mutation CCC,CTC P20L XP_011512793.1
XM_011514492.1 289 Missense Mutation CCC,CTC P20L XP_011512794.1
XM_017010742.1 289 Missense Mutation CCC,CTC P20L XP_016866231.1
XM_017010743.1 289 Intron XP_016866232.1
Gene
LOC102723648
Gene Name
uncharacterized LOC102723648
There are no transcripts associated with this gene.

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