Product Details

SNP ID: rs11040957
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:6681967 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TAAAGACTTTTATCTATTGTGCAAA[C/G]AGAGGGTCATCTGGCTCCCCAGAAG
Phenotype: MIM: 611830
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: MRPL17 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022061.3	784	UTR 3			NP_071344.1