Product Details

SNP ID: rs146193251
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:25224807 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCTTCTGTTTAATTTTTTTTATTA[A/T]GTGTAACTGTGCCAATGATTTTTAT
Phenotype: MIM: 616984
Polymorphism: A/T, Transversion 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	953	UTR 3			NP_071433.3