Product Details

SNP ID: rs150149001
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:159264865 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCAGGGTCACCTGGAACTCAGATG[A/G]TTTCACTCCAAACTCTGCACTACTA
Phenotype: MIM: 609867
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: UBLCP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145049.3		Intron			NP_659486.2