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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131370 MIM: 606672 MIM: 176610 MIM: 610431 MIM: 604165 | ||||||||||||||||||||
Literature Links: |
ENO3 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 |
ENO3 - enolase 3 | ||||||
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There are no transcripts associated with this gene. |
GP1BA - glycoprotein Ib platelet alpha subunit | ||||||
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There are no transcripts associated with this gene. |
PFN1 - profilin 1 | ||||||
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There are no transcripts associated with this gene. |
RNF167 - ring finger protein 167 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320356.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307285.1 | |
NM_001320357.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307286.1 | |
NM_001320358.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307287.1 | |
NM_001320359.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307288.1 | |
NM_001320360.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307289.1 | |
NM_001320361.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_001307290.1 | |
NM_001320362.1 | 629 | Silent Mutation | GTG,GTT | V,V 88 | NP_001307291.1 | |
NM_001320363.1 | 629 | Silent Mutation | GTG,GTT | V,V 88 | NP_001307292.1 | |
NM_001320364.1 | 629 | Silent Mutation | GTG,GTT | V,V 88 | NP_001307293.1 | |
NM_001320365.1 | 629 | Silent Mutation | GTG,GTT | V,V 88 | NP_001307294.1 | |
NM_015528.2 | 629 | Silent Mutation | GTG,GTT | V,V 123 | NP_056343.1 | |
XM_017024427.1 | 629 | Silent Mutation | GTG,GTT | V,V 123 | XP_016879916.1 | |
XM_017024428.1 | 629 | Intron | XP_016879917.1 |
SLC25A11 - solute carrier family 25 member 11 | ||||||
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There are no transcripts associated with this gene. |