Product Details

SNP ID
rs1959149
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34713349 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAATCATTCAGAGGTAGCAACTT[A/C]ACAAAAGATGTGTAGGGGTCCTCTA
Phenotype
MIM: 601443
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CFL2 PubMed Links

Gene Details

Gene
CFL2
Gene Name
cofilin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243645.1 295 Silent Mutation GTG,GTT V55V NP_001230574.1
NM_021914.7 295 Silent Mutation GTG,GTT V72V NP_068733.1
NM_138638.4 295 Silent Mutation GTG,GTT V72V NP_619579.1
XM_011536363.2 295 Silent Mutation GTG,GTT V55V XP_011534665.1

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