Product Details

SNP ID
rs11466112
Assay Type
Functionally tested
NCBI dbSNP Submissions
21
Location
Chr.1:115286135 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAGGCCGTATCTATCCGGATAAACC[A/G]CCAGGCAGCCTGCTTGCCATCCATG
Phenotype
MIM: 162030
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NGF PubMed Links

Gene Details

Gene
NGF
Gene Name
nerve growth factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002506.2 830 Missense Mutation CGG,TGG R221W NP_002497.2
XM_006710663.3 830 Missense Mutation CGG,TGG R221W XP_006710726.1
XM_011541518.2 830 Missense Mutation CGG,TGG R276W XP_011539820.1

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