Product Details

SNP ID: rs3484
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.22:36800827 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: CTGAACAGAAATGCAGGAGGGTGGC[A/G]AGAGGGGCCGAGATTGGGTGTTCAG
Phenotype: MIM: 168890
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PVALB PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001315532.1	446	UTR 3			NP_001302461.1
NM_002854.2	446	UTR 3			NP_002845.1