Product Details

SNP ID
rs142228912
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:60351243 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAAAATACAGGGGCTTGTTCTGAA[G/T]GCACTGAACTGTGGAGAGAAGAAAG
Phenotype
MIM: 151740
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ANXA2 PubMed Links

Gene Details

Gene
ANXA2
Gene Name
annexin A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001002857.1 914 Intron NP_001002857.1
NM_001002858.2 914 Missense Mutation NP_001002858.1
NM_001136015.2 914 Intron NP_001129487.1
NM_004039.2 914 Intron NP_004030.1
XM_011521477.2 914 Intron XP_011519779.1
XM_017022090.1 914 Intron XP_016877579.1
XM_017022091.1 914 Intron XP_016877580.1
XM_017022092.1 914 Intron XP_016877581.1
XM_017022093.1 914 Intron XP_016877582.1

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