Product Details

SNP ID
rs114833521
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:37994870 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAACAAATGGTCTTCCCTGACGGGA[G/T]CTTTTTGTTTTAACACACTGTTTTC
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
VILL PubMed Links

Gene Details

Gene
VILL
Gene Name
villin like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015873.3 Intron NP_056957.3
XM_005265191.3 Intron XP_005265248.1
XM_005265192.4 Intron XP_005265249.1
XM_006713184.3 Intron XP_006713247.1
XM_011533770.2 Intron XP_011532072.1
XM_011533771.1 Intron XP_011532073.1
XM_011533773.2 Intron XP_011532075.1

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