Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGGGTGCCTTGGAGACCATCTGG[C/T]GGCAGCAAGGGCTCTTGGGGCTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 609613 MIM: 610817 | ||||||||||||||||||||
Literature Links: |
PLEKHM2 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 |
PLEKHM2 - pleckstrin homology and RUN domain containing M2 | ||||||
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There are no transcripts associated with this gene. |
SLC25A34 - solute carrier family 25 member 34 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207348.2 | 1873 | Missense Mutation | CGG,TGG | R,W 159 | NP_997231.1 | |
XM_011541292.2 | 1873 | Missense Mutation | CGG,TGG | R,W 159 | XP_011539594.1 | |
XM_011541293.1 | 1873 | Missense Mutation | CGG,TGG | R,W 159 | XP_011539595.1 | |
XM_017001083.1 | 1873 | Missense Mutation | CGG,TGG | R,W 159 | XP_016856572.1 |
TMEM82 - transmembrane protein 82 | ||||||
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There are no transcripts associated with this gene. |