Product Details

SNP ID
rs147153174
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:184164320 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCAGCCCCCTTCTGTGCTGATAA[C/T]CCATCGGAGCTGCCACCACCTATGG
Phenotype
MIM: 601368
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
DVL3 PubMed Links

Gene Details

Gene
DVL3
Gene Name
dishevelled segment polarity protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004423.3 610 Silent Mutation AAC,AAT N95N NP_004414.3
XM_005247172.2 610 Silent Mutation AAC,AAT N95N XP_005247229.1
XM_011512513.2 610 UTR 5 XP_011510815.1

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