Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGCAGAAGCTCTGGGTCACCTGTT[C/T]AGTCACCGCATGGGCTGCTTCGTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611065 | ||||||||||||||||||||
Literature Links: |
PPM1K PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PPM1K - protein phosphatase, Mg2+/Mn2+ dependent 1K | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152542.4 | 706 | Missense Mutation | AAA,GAA | K,E 328 | NP_689755.3 | |
XM_005262775.3 | 706 | Intron | XP_005262832.1 | |||
XM_006714111.3 | 706 | Missense Mutation | AAA,GAA | K,E 328 | XP_006714174.1 | |
XM_017007803.1 | 706 | Missense Mutation | AAA,GAA | K,E 328 | XP_016863292.1 | |
XM_017007804.1 | 706 | Missense Mutation | AAA,GAA | K,E 219 | XP_016863293.1 | |
XM_017007805.1 | 706 | Missense Mutation | AAA,GAA | K,E 219 | XP_016863294.1 | |
XM_017007806.1 | 706 | Missense Mutation | AAA,GAA | K,E 219 | XP_016863295.1 | |
XM_017007807.1 | 706 | Missense Mutation | AAA,GAA | K,E 200 | XP_016863296.1 |