Product Details

SNP ID
rs139946152
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15867489 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAAGATCTTCAATGTTAGTACTT[C/T]TCTGTTCCTCCTTTCTTAGGTGGTC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FOPNL PubMed Links

Gene Details

Gene
FOPNL
Gene Name
FGFR1OP N-terminal like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304497.1 342 Missense Mutation AAA,AGA K85R NP_001291426.1
NM_001304498.1 342 UTR 3 NP_001291427.1
NM_001304499.1 342 Missense Mutation AAA,AGA K183R NP_001291428.1
NM_001304500.1 342 Missense Mutation AAA,AGA K93R NP_001291429.1
NM_001304502.1 342 UTR 3 NP_001291431.1
NM_144600.3 342 Missense Mutation AAA,AGA K159R NP_653201.1

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