Product Details

SNP ID: rs12124430
Assay Type: Functionally tested
NCBI dbSNP Submissions: 18
Location: Chr.1:61685154 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AATATATTATATTAGGATAAAATTC[G/T]GTAGAAGAGGAATAAAAATAAAAAT
Phenotype: MIM: 610080
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: TM2D1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032027.2		Intron			NP_114416.1