Product Details

SNP ID
rs11024773
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:18728950 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAAGCGCAGTCATTCTGGGGACTGG[C/T]GGGACAGCTGCTTTTCGTAGAGGCT
Phenotype
MIM: 176879
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
IGSF22 PubMed Links

Gene Details

Gene
IGSF22
Gene Name
immunoglobulin superfamily member 22
There are no transcripts associated with this gene.

Gene
PTPN5
Gene Name
protein tyrosine phosphatase, non-receptor type 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039970.1 2851 Missense Mutation CAC,CGC H529R NP_001035059.1
NM_001278236.1 2851 Missense Mutation CAC,CGC H529R NP_001265165.1
NM_001278238.1 2851 Missense Mutation CAC,CGC H537R NP_001265167.1
NM_001278239.1 2851 Missense Mutation CAC,CGC H505R NP_001265168.1
NM_006906.1 2851 Missense Mutation CAC,CGC H561R NP_008837.1
NM_032781.3 2851 Missense Mutation CAC,CGC H561R NP_116170.3
XM_011520411.2 2851 UTR 3 XP_011518713.1
XM_017018434.1 2851 Silent Mutation CCA,CCG P507P XP_016873923.1
XM_017018435.1 2851 Silent Mutation CCA,CCG P507P XP_016873924.1
XM_017018436.1 2851 Silent Mutation CCA,CCG P483P XP_016873925.1
XM_017018437.1 2851 Silent Mutation CCA,CCG P475P XP_016873926.1
XM_017018438.1 2851 Silent Mutation CCA,CCG P468P XP_016873927.1
XM_017018439.1 2851 Silent Mutation CCA,CCG P451P XP_016873928.1
XM_017018440.1 2851 Missense Mutation CAC,CGC H523R XP_016873929.1
XM_017018441.1 2851 Intron XP_016873930.1

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