Product Details

SNP ID
rs202138909
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:115286354 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTTGCCCTTGATGTCTGTGGCGG[T/G]GGTCTTATCCCCAACCCACACGCTG
Phenotype
MIM: 162030
Polymorphism
T/G, Transversion 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_002506.2 611 Missense Mutation ACC,CCC T148P NP_002497.2
XM_006710663.3 611 Missense Mutation ACC,CCC T148P XP_006710726.1
XM_011541518.2 611 Missense Mutation ACC,CCC T203P XP_011539820.1

View Full Product Details