Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACATCTGTGCATCTTGACCACCTC[C/T]GTGTCTATTGGCAGGAACTGCTTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615499 | ||||||||||||||||||||
Literature Links: |
PDP2 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 |
PDP2 - pyruvate dehyrogenase phosphatase catalytic subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005256064.4 | 957 | Missense Mutation | CGT,TGT | R,C 210 | XP_005256121.1 | |
XM_005256066.4 | 957 | Missense Mutation | CGT,TGT | R,C 210 | XP_005256123.1 | |
XM_005256067.4 | 957 | Missense Mutation | CGT,TGT | R,C 210 | XP_005256124.1 | |
XM_005256068.4 | 957 | Missense Mutation | CGT,TGT | R,C 210 | XP_005256125.1 | |
XM_017023506.1 | 957 | Missense Mutation | CGT,TGT | R,C 210 | XP_016878995.1 |