Product Details

SNP ID: rs4820249
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:36801288 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AATATCTTATTTGACTCTGACAATA[A/G]TCCTGTCTGGTGCATTTTGGCATTG
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		Intron			NP_001302461.1
NM_002854.2		Intron			NP_002845.1