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AAGGCAAACTGCTTTTCTAAACTTG[C/G]AAAGCCTCCCACCATATGCAAAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610701 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ENO4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ENO4 - enolase family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242699.1 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | NP_001229628.1 | |
XM_005269815.3 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | XP_005269872.1 | |
XM_006717835.3 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | XP_006717898.1 | |
XM_006717836.3 | 1525 | Intron | XP_006717899.1 | |||
XM_011539797.2 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | XP_011538099.1 | |
XM_011539799.2 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | XP_011538101.1 | |
XM_017016241.1 | 1525 | Missense Mutation | GCA,GGA | A,G 63 | XP_016871730.1 |
HSPA12A - heat shock protein family A (Hsp70) member 12A | ||||||
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There are no transcripts associated with this gene. |