Product Details

SNP ID: rs144268706
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:197705942 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTCCGACGAGTGCTTCCTGCCTGA[A/G]GCCAAGGTCACCCAGCAGCCGGGCC
Phenotype: MIM: 609728
Polymorphism: A/G, Transition 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	639	Silent Mutation	GAA,GAG	E179E	NP_612404.1