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CTCCAGGCTCTTCCACCCGTGGACC[A/G]CCGACATGCCGGCGCACTCGCCAGG
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 | |||
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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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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 | 389 | Missense Mutation | ACC,GCC | T,A 75 | NP_001003845.1 | |
XM_005246542.4 | 389 | Missense Mutation | ACC,GCC | T,A 119 | XP_005246599.1 | |
XM_011511159.2 | 389 | Missense Mutation | ACC,GCC | T,A 131 | XP_011509461.1 |