Product Details

SNP ID
rs148935179
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15866184 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAAGTTTCTGCATTTAGATAAAAA[C/T]TCTTGGCTAATCTGTAAGAAGTGAA
Phenotype
MIM: 160745
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 1647 UTR 3 NP_001291426.1
NM_001304498.1 1647 UTR 3 NP_001291427.1
NM_001304499.1 1647 UTR 3 NP_001291428.1
NM_001304500.1 1647 UTR 3 NP_001291429.1
NM_001304502.1 1647 UTR 3 NP_001291431.1
NM_144600.3 1647 UTR 3 NP_653201.1
Gene
MYH11
Gene Name
myosin heavy chain 11
There are no transcripts associated with this gene.

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