Product Details

SNP ID

rs34990078

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:107861801 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTCCTCTTGCAGTCCTGCAGGAC[A/G]GTGCTGAAGGTGATGTGGGGGTACT

Phenotype

MIM: 609083

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FBXL17 PubMed Links

Gene Details

Gene

FBXL17

Gene Name

F-box and leucine rich repeat protein 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163315.2	2432	Silent Mutation	ACC,ACT	T675T	NP_001156787.2
XM_005272048.4	2432	Intron			XP_005272105.1
XM_005272050.4	2432	Intron			XP_005272107.1
XM_011543574.2	2432	Intron			XP_011541876.1
XM_011543575.2	2432	Intron			XP_011541877.1
XM_011543576.2	2432	Intron			XP_011541878.1
XM_011543577.2	2432	Intron			XP_011541879.1
XM_011543578.2	2432	Intron			XP_011541880.1
XM_011543579.2	2432	Intron			XP_011541881.1
XM_011543580.2	2432	Intron			XP_011541882.1
XM_017009729.1	2432	Intron			XP_016865218.1

View Full Product Details