Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176879 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGSF22 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
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Global
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Caucasian
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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IGSF22 - immunoglobulin superfamily member 22 | ||||||
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There are no transcripts associated with this gene. |
PTPN5 - protein tyrosine phosphatase, non-receptor type 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039970.1 | 2732 | Silent Mutation | GTA,GTG | V,V 489 | NP_001035059.1 | |
NM_001278236.1 | 2732 | Silent Mutation | GTA,GTG | V,V 489 | NP_001265165.1 | |
NM_001278238.1 | 2732 | Silent Mutation | GTA,GTG | V,V 497 | NP_001265167.1 | |
NM_001278239.1 | 2732 | Silent Mutation | GTA,GTG | V,V 465 | NP_001265168.1 | |
NM_006906.1 | 2732 | Silent Mutation | GTA,GTG | V,V 521 | NP_008837.1 | |
NM_032781.3 | 2732 | Silent Mutation | GTA,GTG | V,V 521 | NP_116170.3 | |
XM_011520411.2 | 2732 | Silent Mutation | GTA,GTG | V,V 521 | XP_011518713.1 | |
XM_017018434.1 | 2732 | Missense Mutation | AGT,GGT | S,G 468 | XP_016873923.1 | |
XM_017018435.1 | 2732 | Missense Mutation | AGT,GGT | S,G 468 | XP_016873924.1 | |
XM_017018436.1 | 2732 | Missense Mutation | AGT,GGT | S,G 444 | XP_016873925.1 | |
XM_017018437.1 | 2732 | Missense Mutation | AGT,GGT | S,G 436 | XP_016873926.1 | |
XM_017018438.1 | 2732 | Missense Mutation | AGT,GGT | S,G 429 | XP_016873927.1 | |
XM_017018439.1 | 2732 | Missense Mutation | AGT,GGT | S,G 412 | XP_016873928.1 | |
XM_017018440.1 | 2732 | Missense Mutation | AGT,GGT | S,G 468 | XP_016873929.1 | |
XM_017018441.1 | 2732 | Intron | XP_016873930.1 |