Product Details

SNP ID
rs150768738
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119357206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCACCTGGAGTCGTTGAAAGTGT[A/G]CCATTCTCCTGTCCCTGGACTGCGA
Phenotype
MIM: 604725
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
USP2 PubMed Links

Gene Details

Gene
USP2
Gene Name
ubiquitin specific peptidase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243759.1 967 Missense Mutation CAC,TAC H328Y NP_001230688.1
NM_004205.4 967 Missense Mutation CAC,TAC H571Y NP_004196.4
NM_171997.2 967 Missense Mutation CAC,TAC H362Y NP_741994.1
XM_005271721.4 967 Missense Mutation CAC,TAC H571Y XP_005271778.1
XM_005271722.2 967 Missense Mutation CAC,TAC H571Y XP_005271779.1
XM_017018539.1 967 Missense Mutation CAC,TAC H318Y XP_016874028.1

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