Product Details

SNP ID
rs141570789
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.1:93460221 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTTCATGGATGGGATTACAGCCC[C/T]TATAAAAGGACTTGAAGGAGAGAGT
Phenotype
MIM: 608848
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FNBP1L PubMed Links

Gene Details

Gene
FNBP1L
Gene Name
formin binding protein 1 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024948.2 Intron NP_001020119.1
NM_001164473.2 Intron NP_001157945.1
NM_017737.4 Intron NP_060207.2
XM_011541625.2 Intron XP_011539927.1
XM_017001533.1 Intron XP_016857022.1

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