Product Details

SNP ID: rs149306114
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:18157736 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCTGAGTCCTCGCAGTCCCCGGCA[A/G]ATCTTGAAGAAAAGAAGGAAGAAGA
Phenotype: MIM: 607057
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: USP18 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017414.3	443	Missense Mutation	AAT,GAT	N25D	NP_059110.2
XM_006724074.2	443	UTR 5			XP_006724137.1