Product Details

SNP ID

rs150136942

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:115286512 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGATCCTGAGTGTCTGCAGCTTCA[C/T]GGGGAGGCTGGGTGCTAAACAGCAC

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	453	Missense Mutation	CAT,CGT	H95R	NP_002497.2
XM_006710663.3	453	Missense Mutation	CAT,CGT	H95R	XP_006710726.1
XM_011541518.2	453	Missense Mutation	CAT,CGT	H150R	XP_011539820.1

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