Product Details

SNP ID: rs199905823
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:25226788 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTTCTCCCAAACCTTTGGGGCAGG[C/T]TAGGAACACGTCTCACGAGGCTCAC
Phenotype: MIM: 616984
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NPVF PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022150.3	424	Missense Mutation	AAC,AGC	N126S	NP_071433.3