Product Details

SNP ID: rs147988641
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:75899571 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCAATCGGCTGGTCCTGCTTGAAGA[A/G]CAGGAAGGCAAGACGGTGGATGCCG
Phenotype: MIM: 611844
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MRPL38 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032478.3	1039	Missense Mutation	CTC,TTC	L272F	NP_115867.2

There are no transcripts associated with this gene.