Product Details

SNP ID: rs17689640
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:75649189 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AATGTTATAAAAATACAAAGTTGGA[A/G]AAAAGTCCTAGTCTGAGAGACTAAT
Phenotype: MIM: 611832
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MRPL19 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014763.3		Intron			NP_055578.2