Product Details

SNP ID: rs12660899
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:36399739 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTCCTGCCAAATACAGGTTGTTTCG[G/T]AGGAAAACTAAGTTAGCTGTGGATT
Phenotype
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: PXT1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152990.3		Intron			NP_694535.2
XM_011514400.2		Intron			XP_011512702.1