Product Details

SNP ID
rs144788470
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:65530029 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCCGGCCTTCATACATCGGGAGCA[C/T]CGTCTCATCCTCCCAGATCTCCTCA
Phenotype
MIM: 604025
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
AXIN2 PubMed Links

Gene Details

Gene
AXIN2
Gene Name
axin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004655.3 2979 Missense Mutation ATG,GTG M827V NP_004646.3
XM_011525319.2 2979 Missense Mutation ATG,GTG M827V XP_011523621.1
XM_011525320.1 2979 Missense Mutation ATG,GTG M827V XP_011523622.1
XM_011525321.2 2979 Missense Mutation ATG,GTG M827V XP_011523623.1
XM_017025192.1 2979 Missense Mutation ATG,GTG M827V XP_016880681.1
XM_017025193.1 2979 Missense Mutation ATG,GTG M762V XP_016880682.1
XM_017025194.1 2979 Missense Mutation ATG,GTG M762V XP_016880683.1

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