Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTGCGTGGCCGCCGAGACCACGC[A/G]GGAGGTGATCTGGTGGGACAAACGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603183 | ||||||||||||||||||||
Literature Links: |
PPM1N 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 |
PPM1N - protein phosphatase, Mg2+/Mn2+ dependent 1N (putative) | ||||||
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There are no transcripts associated with this gene. |
RTN2 - reticulon 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005619.4 | 1542 | Missense Mutation | CGC,TGC | R,C 438 | NP_005610.1 | |
NM_206900.2 | 1542 | Missense Mutation | CGC,TGC | R,C 365 | NP_996783.1 | |
NM_206901.2 | 1542 | Missense Mutation | CGC,TGC | R,C 98 | NP_996784.1 |