Product Details

SNP ID: rs834996
Assay Type: Functionally tested
NCBI dbSNP Submissions: 63
Location: Chr.1:99647180 on Build GRCh38
Set Membership: HapMap JSNP
Context Sequence [VIC/FAM]: GAAATCTGTGTCACAATCATTTATC[A/C]CTAGCTATAACTTTTGATGTAATTG
Phenotype: MIM: 610182
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: PALMD PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017734.4		Intron			NP_060204.1