Product Details

SNP ID
rs147649568
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:100155081 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTGCCATTTCTTCCATGCATACT[G/T]GAATATCTTGCAGTTTATTGTTGCT
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
LRRC39 PubMed Links

Gene Details

Gene
LRRC39
Gene Name
leucine rich repeat containing 39
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256385.1 1056 Missense Mutation CAA,CCA Q261P NP_001243314.1
NM_001256386.1 1056 Missense Mutation CAA,CCA Q261P NP_001243315.1
NM_001256387.1 1056 Missense Mutation CAA,CCA Q261P NP_001243316.1
NM_144620.3 1056 Missense Mutation CAA,CCA Q261P NP_653221.1
Gene
TRMT13
Gene Name
tRNA methyltransferase 13 homolog
There are no transcripts associated with this gene.

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