Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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 |
---|---|---|
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 |
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 | 1375 | Missense Mutation | AGA,AGC | R,S 433 | NP_001001890.1 | |
NM_001122607.1 | 1375 | Intron | NP_001116079.1 | |||
NM_001754.4 | 1375 | Missense Mutation | AGA,AGC | R,S 460 | NP_001745.2 | |
XM_005261068.3 | 1375 | Missense Mutation | AGA,AGC | R,S 448 | XP_005261125.1 | |
XM_005261069.4 | 1375 | Missense Mutation | AGA,AGC | R,S 396 | XP_005261126.1 | |
XM_011529766.2 | 1375 | Missense Mutation | AGA,AGC | R,S 460 | XP_011528068.1 | |
XM_011529767.2 | 1375 | Missense Mutation | AGA,AGC | R,S 447 | XP_011528069.1 | |
XM_011529768.2 | 1375 | Missense Mutation | AGA,AGC | R,S 383 | XP_011528070.1 | |
XM_011529770.2 | 1375 | Intron | XP_011528072.1 | |||
XM_017028487.1 | 1375 | Missense Mutation | AGA,AGC | R,S 409 | XP_016883976.1 |