Product Details

SNP ID
rs112799998
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:135185910 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCATTCTTATTTCTGCAGCATATAT[A/G]GCAGTGACGAGGATGATGAGGACTT
Phenotype
MIM: 189990
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MYB PubMed Links

Gene Details

Gene
MYB
Gene Name
MYB proto-oncogene, transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130172.1 230 Missense Mutation AGC,GGC S11G NP_001123644.1
NM_001130173.1 230 Missense Mutation AGC,GGC S11G NP_001123645.1
NM_001161656.1 230 Missense Mutation AGC,GGC S11G NP_001155128.1
NM_001161657.1 230 Missense Mutation AGC,GGC S11G NP_001155129.1
NM_001161658.1 230 Missense Mutation AGC,GGC S11G NP_001155130.1
NM_001161659.1 230 Missense Mutation AGC,GGC S11G NP_001155131.1
NM_001161660.1 230 Missense Mutation AGC,GGC S11G NP_001155132.1
NM_005375.3 230 Missense Mutation AGC,GGC S11G NP_005366.2

View Full Product Details