Product Details

SNP ID
rs201699665
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:112515118 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTTGTGCATGCGGTTTCGCTCGC[G/T]GTTGTTGGCCTTCAGTCTACGGGTC
Phenotype
MIM: 606624
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
NEUROG2 PubMed Links

Gene Details

Gene
NEUROG2
Gene Name
neurogenin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024019.3 685 Missense Mutation AGC,CGC S120R NP_076924.1

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