Product Details

SNP ID

rs139830389

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:115286314 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACACTGTTGTTAATGTTCACCTCT[C/G]CCAACACCATCACCTCCTTGCCCTT

Phenotype

MIM: 162030

Polymorphism

C/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	651	Missense Mutation	GCA,GGA	A161G	NP_002497.2
XM_006710663.3	651	Missense Mutation	GCA,GGA	A161G	XP_006710726.1
XM_011541518.2	651	Missense Mutation	GCA,GGA	A216G	XP_011539820.1

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