Product Details

SNP ID
rs146079228
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:38805468 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTTTGGCGTTAGGGCCTTGGCCC[A/C]AGAGAGGACGCCGAGCGCTCCACGG
Phenotype
MIM: 164740
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ETS2 PubMed Links

Gene Details

Gene
ETS2
Gene Name
ETS proto-oncogene 2, transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256295.1 162 Missense Mutation CAA,CCA Q41P NP_001243224.1
NM_005239.5 162 Intron NP_005230.1
XM_005260935.1 162 Intron XP_005260992.1
XM_017028290.1 162 Intron XP_016883779.1

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