Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACTGGACTGTGGGTCGCAGCAGCC[A/G]TGCCCACTTCCAACAGAGTCGTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607126 | ||||||||||||||||||||
Literature Links: |
PLPP2 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 |
PLPP2 - phospholipid phosphatase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003712.3 | 676 | Missense Mutation | CGG,TGG | R,W 193 | NP_003703.1 | |
NM_177526.2 | 676 | Missense Mutation | CGG,TGG | R,W 137 | NP_803545.1 | |
NM_177543.2 | 676 | Missense Mutation | CGG,TGG | R,W 214 | NP_808211.1 | |
XM_011528396.2 | 676 | Missense Mutation | CGG,TGG | R,W 199 | XP_011526698.1 |