Product Details

SNP ID
rs17849799
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:63156467 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGGACTTTGTACTAGGCGTTTCT[C/T]TTTATGTTTTTTCTTTTCCTCTTCC
Phenotype
MIM: 612055
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
RPS27L PubMed Links

Gene Details

Gene
RPS27L
Gene Name
ribosomal protein S27 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015920.3 198 Missense Mutation AAG,GAG K21E NP_057004.1

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