Product Details

SNP ID: rs17037234
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:69896432 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTCTAACATCTTTGCTTATAAATA[C/T]TAGATCTCCAAGACGACATAGATCC
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SNRNP27 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006857.2		Intron			NP_006848.1