Product Details

SNP ID
rs34542615
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:115286119 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGAGCACACACACACAGGCCGTA[C/T]CTATCCGGATAAACCGCCAGGCAGC
Phenotype
MIM: 162030
Polymorphism
C/T, 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_002506.2 846 Missense Mutation GAT,GGT D226G NP_002497.2
XM_006710663.3 846 Missense Mutation GAT,GGT D226G XP_006710726.1
XM_011541518.2 846 Missense Mutation GAT,GGT D281G XP_011539820.1

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