Product Details

SNP ID
rs150474088
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:204618237 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTACTCCGTGGCCTGAAGGAGGC[A/G]GGTAATGTTGTAGCTGTGGGTTCCC
Phenotype
MIM: 605492
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC105371692 PubMed Links

Gene Details

Gene
LOC105371692
Gene Name
uncharacterized LOC105371692
There are no transcripts associated with this gene.

Gene
LRRN2
Gene Name
leucine rich repeat neuronal 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006338.2 2214 Missense Mutation CGC,TGC R586C NP_006329.2
NM_201630.1 2214 Missense Mutation CGC,TGC R586C NP_963924.1
XM_005244827.3 2214 Missense Mutation CGC,TGC R586C XP_005244884.1
XM_011509066.2 2214 Missense Mutation CGC,TGC R586C XP_011507368.1
XM_017000050.1 2214 Missense Mutation CGC,TGC R586C XP_016855539.1

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