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GGCGCGCGGAGGGCGCCATGTTGGT[C/G]GGGGAGTTGCTGTGGCTGCCCTCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 151385 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINC01426 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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LINC01426 - long intergenic non-protein coding RNA 1426 | ||||||
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There are no transcripts associated with this gene. |
RUNX1 - runt related transcription factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001890.2 | 1384 | Silent Mutation | CCC,CCG | P,P 436 | NP_001001890.1 | |
NM_001122607.1 | 1384 | Intron | NP_001116079.1 | |||
NM_001754.4 | 1384 | Silent Mutation | CCC,CCG | P,P 463 | NP_001745.2 | |
XM_005261068.3 | 1384 | Silent Mutation | CCC,CCG | P,P 451 | XP_005261125.1 | |
XM_005261069.4 | 1384 | Silent Mutation | CCC,CCG | P,P 399 | XP_005261126.1 | |
XM_011529766.2 | 1384 | Silent Mutation | CCC,CCG | P,P 463 | XP_011528068.1 | |
XM_011529767.2 | 1384 | Silent Mutation | CCC,CCG | P,P 450 | XP_011528069.1 | |
XM_011529768.2 | 1384 | Silent Mutation | CCC,CCG | P,P 386 | XP_011528070.1 | |
XM_011529770.2 | 1384 | Intron | XP_011528072.1 | |||
XM_017028487.1 | 1384 | Silent Mutation | CCC,CCG | P,P 412 | XP_016883976.1 |