Product Details

SNP ID: rs138604676
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:197706089 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCCACTCCAGCGGTGGCTGCGGGG[A/C]AACCCTCAGGCGATCACCCCCGAAC
Phenotype: MIM: 609728
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: MARS2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138395.3	786	Silent Mutation	GGA,GGC	G228G	NP_612404.1