Product Details

SNP ID
rs148892073
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:152658006 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTATCCTTCTCTCGCTCAGCATC[G/A]GATTCTGGAGAGTCCTGTATGAATA
Phenotype
MIM: 616285 MIM: 612941
Polymorphism
G/A, Transition substitution
Allele Nomenclature
Literature Links
FMNL2 PubMed Links

Gene Details

Gene
FMNL2
Gene Name
formin like 2
There are no transcripts associated with this gene.

Gene
PRPF40A
Gene Name
pre-mRNA processing factor 40 homolog A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017892.3 2822 Silent Mutation TCC,TCT S861S NP_060362.3
XM_005246676.4 2822 Silent Mutation TCC,TCT S967S XP_005246733.3
XM_005246677.4 2822 Silent Mutation TCC,TCT S865S XP_005246734.2
XM_011511446.2 2822 Silent Mutation TCC,TCT S953S XP_011509748.1
XM_011511447.2 2822 Silent Mutation TCC,TCT S971S XP_011509749.1
XM_011511448.2 2822 Silent Mutation TCC,TCT S847S XP_011509750.1
XM_011511449.2 2822 Silent Mutation TCC,TCT S809S XP_011509751.1
XM_017004453.1 2822 Silent Mutation TCC,TCT S971S XP_016859942.1
XM_017004454.1 2822 Silent Mutation TCC,TCT S949S XP_016859943.1
XM_017004455.1 2822 Silent Mutation TCC,TCT S843S XP_016859944.1
XM_017004456.1 2822 Silent Mutation TCC,TCT S809S XP_016859945.1
XM_017004457.1 2822 Silent Mutation TCC,TCT S805S XP_016859946.1
XM_017004458.1 2822 Silent Mutation TCC,TCT S791S XP_016859947.1
XM_017004459.1 2822 Silent Mutation TCC,TCT S791S XP_016859948.1
XM_017004460.1 2822 Silent Mutation TCC,TCT S787S XP_016859949.1
XM_017004461.1 2822 Silent Mutation TCC,TCT S787S XP_016859950.1

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