Product Details

SNP ID
rs146463638
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:228408267 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCAGACTTCGGAGCCCCCAGGCA[C/G]AAGAAAGGCTGCAGGGGGCCTGGGA
Phenotype
MIM: 607868 MIM: 606123
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TRIM11 PubMed Links

Gene Details

Gene
TRIM11
Gene Name
tripartite motif containing 11
There are no transcripts associated with this gene.

Gene
TRIM17
Gene Name
tripartite motif containing 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024940.2 2285 Missense Mutation TTC,TTG F456L NP_001020111.1
NM_001134855.1 2285 Intron NP_001128327.1
NM_016102.3 2285 Missense Mutation TTC,TTG F456L NP_057186.1
XM_006711779.2 2285 Missense Mutation TTC,TTG F456L XP_006711842.1
XM_011544209.2 2285 Missense Mutation TTC,TTG F456L XP_011542511.1
XM_011544210.2 2285 Missense Mutation TTC,TTG F456L XP_011542512.1
XM_011544211.2 2285 Missense Mutation TTC,TTG F429L XP_011542513.1
XM_017001418.1 2285 UTR 3 XP_016856907.1
XM_017001419.1 2285 UTR 3 XP_016856908.1

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