Product Details

SNP ID
rs187786999
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:169795558 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAAGTGAGATTTGTTTTCATTGAT[G/T]GTGAAAGTGCAACAAGTCCTTCTCC
Phenotype
MIM: 606042
Polymorphism
G/T, Transversion 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 1086 Missense Mutation NP_001166250.1
NM_001172780.1 1086 Intron NP_001166251.1
NM_153353.4 1086 Missense Mutation NP_699184.2
XM_006713508.3 1086 Missense Mutation XP_006713571.1
XM_011512442.2 1086 Missense Mutation XP_011510744.1
XM_017005746.1 1086 Missense Mutation XP_016861235.1
Gene
MYNN
Gene Name
myoneurin
There are no transcripts associated with this gene.

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