Product Details

SNP ID
rs149500546
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:169795588 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTGCAACAAGTCCTTCTCCCTCT[A/G]TGTTGTTGCTGACTACTGACAACCT
Phenotype
MIM: 606042
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LRRC34 PubMed Links

Gene Details

Gene
LRRC34
Gene Name
leucine rich repeat containing 34
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172779.1 1056 Missense Mutation ACA,ATA T363I NP_001166250.1
NM_001172780.1 1056 Intron NP_001166251.1
NM_153353.4 1056 Missense Mutation ACA,ATA T331I NP_699184.2
XM_006713508.3 1056 Missense Mutation ACA,ATA T345I XP_006713571.1
XM_011512442.2 1056 Missense Mutation ACA,ATA T362I XP_011510744.1
XM_017005746.1 1056 Missense Mutation ACA,ATA T301I XP_016861235.1
Gene
MYNN
Gene Name
myoneurin
There are no transcripts associated with this gene.

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