Product Details

SNP ID: rs200000186
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:112514859 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCACGTGGAGGCGGGCGAGGGGCTG[A/T]CTCCGCTGCTGCTCAGGGCGGCGCT
Phenotype: MIM: 606624
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: NEUROG2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024019.3	944	Missense Mutation	GAC,GTC	D206V	NP_076924.1