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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