Product Details

SNP ID
rs140413541
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:224379731 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAAGGACACTGTTGTTTTTGGAGG[C/T]AGCCACCCCCAAGGAAGAGGCTGGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM124B PubMed Links

Gene Details

Gene
FAM124B
Gene Name
family with sequence similarity 124 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001122779.1 1561 Missense Mutation ACC,GCC T404A NP_001116251.1
NM_024785.2 1561 UTR 3 NP_079061.2

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