Product Details

SNP ID: rs148072754
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:112514726 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTTGTCGGGAGGTGGGGGCTGCCA[A/G]TAGTCCATGTCTGACCCGGCCGGGC
Phenotype: MIM: 606624
Polymorphism: A/G, Transition 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	1077	Silent Mutation	TAC,TAT	Y250Y	NP_076924.1