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CGCTGACCAGGCGCGGGAGCCCCAG[C/G]GTCCGCTTCGAGGACGGTGCTGTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 603768 MIM: 610538 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPP1R12B 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PPP1R12B - protein phosphatase 1 regulatory subunit 12B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167857.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | NP_001161329.1 | |
NM_001167858.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | NP_001161330.1 | |
NM_001197131.1 | 309 | Intron | NP_001184060.1 | |||
NM_002481.3 | 309 | Missense Mutation | AGC,AGG | S,R 53 | NP_002472.2 | |
NM_032103.2 | 309 | Intron | NP_115286.1 | |||
NM_032104.2 | 309 | Intron | NP_115287.1 | |||
XM_005245206.4 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_005245263.1 | |
XM_017001342.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856831.1 | |
XM_017001343.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856832.1 | |
XM_017001344.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856833.1 | |
XM_017001345.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856834.1 | |
XM_017001346.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856835.1 | |
XM_017001347.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856836.1 | |
XM_017001348.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856837.1 | |
XM_017001349.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856838.1 | |
XM_017001350.1 | 309 | UTR 5 | XP_016856839.1 | |||
XM_017001351.1 | 309 | Missense Mutation | AGC,AGG | S,R 53 | XP_016856840.1 | |
XM_017001352.1 | 309 | Intron | XP_016856841.1 | |||
XM_017001353.1 | 309 | Intron | XP_016856842.1 | |||
XM_017001354.1 | 309 | Intron | XP_016856843.1 | |||
XM_017001355.1 | 309 | Intron | XP_016856844.1 |
UBE2T - ubiquitin conjugating enzyme E2 T | ||||||
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There are no transcripts associated with this gene. |