Product Details

SNP ID
rs191921902
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:74073627 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATGTCTGTCCCAAGAAGCTAGAG[C/T]TGTCAGAGGGTGTGGCAGGCGATCT
Phenotype
MIM: 609093
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXO15 PubMed Links

Gene Details

Gene
FBXO15
Gene Name
F-box protein 15
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142958.1 1457 Missense Mutation AAC,AGC N456S NP_001136430.1
NM_152676.2 1457 Missense Mutation AAC,AGC N380S NP_689889.1
XM_011525856.1 1457 Missense Mutation AAC,AGC N386S XP_011524158.1
XM_011525858.2 1457 Intron XP_011524160.1
XM_011525859.1 1457 Intron XP_011524161.1
XM_011525860.1 1457 Intron XP_011524162.1
XM_017025603.1 1457 Missense Mutation AAC,AGC N380S XP_016881092.1
XM_017025604.1 1457 Missense Mutation AAC,AGC N380S XP_016881093.1

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