Product Details

SNP ID: rs978095
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:25224937 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAGACAAAAATCATTTTAACTTTA[C/T]GTAACAAATATGCTTTAATTTTTTT
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	823	UTR 3			NP_071433.3