Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAGCGCAGTCATTCTGGGGACTGG[C/T]GGGACAGCTGCTTTTCGTAGAGGCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 176879 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGSF22 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
|
Chinese - Not Available | CHB (Han Chinese)
|
||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
IGSF22 - immunoglobulin superfamily member 22 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PTPN5 - protein tyrosine phosphatase, non-receptor type 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039970.1 | 2851 | Missense Mutation | CAC,CGC | H,R 529 | NP_001035059.1 | |
NM_001278236.1 | 2851 | Missense Mutation | CAC,CGC | H,R 529 | NP_001265165.1 | |
NM_001278238.1 | 2851 | Missense Mutation | CAC,CGC | H,R 537 | NP_001265167.1 | |
NM_001278239.1 | 2851 | Missense Mutation | CAC,CGC | H,R 505 | NP_001265168.1 | |
NM_006906.1 | 2851 | Missense Mutation | CAC,CGC | H,R 561 | NP_008837.1 | |
NM_032781.3 | 2851 | Missense Mutation | CAC,CGC | H,R 561 | NP_116170.3 | |
XM_011520411.2 | 2851 | UTR 3 | XP_011518713.1 | |||
XM_017018434.1 | 2851 | Silent Mutation | CCA,CCG | P,P 507 | XP_016873923.1 | |
XM_017018435.1 | 2851 | Silent Mutation | CCA,CCG | P,P 507 | XP_016873924.1 | |
XM_017018436.1 | 2851 | Silent Mutation | CCA,CCG | P,P 483 | XP_016873925.1 | |
XM_017018437.1 | 2851 | Silent Mutation | CCA,CCG | P,P 475 | XP_016873926.1 | |
XM_017018438.1 | 2851 | Silent Mutation | CCA,CCG | P,P 468 | XP_016873927.1 | |
XM_017018439.1 | 2851 | Silent Mutation | CCA,CCG | P,P 451 | XP_016873928.1 | |
XM_017018440.1 | 2851 | Missense Mutation | CAC,CGC | H,R 523 | XP_016873929.1 | |
XM_017018441.1 | 2851 | Intron | XP_016873930.1 |