Product Details

SNP ID: rs60142768
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:25224767 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCATACTATTTAATTTCCATCATA[A/T]TGTTTTTCAGGGTGCTCTTCTGTTT
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	993	UTR 3			NP_071433.3