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CCCCGAGGCGGAGCCGGGGAAGAAG[A/C]AGCAGCACGTGTGCCACGTGCCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609391 | ||||||||||||||||||||
Literature Links: |
LINC01124 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 |
LINC01124 - long intergenic non-protein coding RNA 1124 | ||||||
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There are no transcripts associated with this gene. |
LOC101926913 - uncharacterized LOC101926913 | ||||||
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There are no transcripts associated with this gene. |
SP5 - Sp5 transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003845.2 | 1046 | Missense Mutation | AAG,CAG | K,Q 294 | NP_001003845.1 | |
XM_005246542.4 | 1046 | Missense Mutation | AAG,CAG | K,Q 338 | XP_005246599.1 | |
XM_011511159.2 | 1046 | Missense Mutation | AAG,CAG | K,Q 350 | XP_011509461.1 |