Product Details

SNP ID: rs6736380
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:38670681 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATACGTCTCTGATCAGAGGGAGCAA[C/T]TAATCATTTTTATCCCCTTTCTTTC
Phenotype: MIM: 137030
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GALM PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138801.2		Intron			NP_620156.1
XM_011532540.1		Intron			XP_011530842.1