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GGCTTCCACTGCGTGTCTAGGAAGC[A/G]CTCTTTCAGGATGCTCTGAGGCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601801 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724532 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC102724532 - uncharacterized LOC102724532 | ||||||
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There are no transcripts associated with this gene. |
SP2 - Sp2 transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003110.5 | Intron | NP_003101.3 | ||||
XM_006722023.2 | Intron | XP_006722086.1 | ||||
XM_006722025.2 | Intron | XP_006722088.1 | ||||
XM_006722026.2 | Intron | XP_006722089.1 | ||||
XM_006722027.2 | Intron | XP_006722090.1 | ||||
XM_011525136.2 | Intron | XP_011523438.1 | ||||
XM_011525137.2 | Intron | XP_011523439.1 | ||||
XM_011525138.2 | Intron | XP_011523440.1 | ||||
XM_011525139.2 | Intron | XP_011523441.1 | ||||
XM_011525140.2 | Intron | XP_011523442.1 | ||||
XM_011525142.1 | Intron | XP_011523444.1 | ||||
XM_011525143.1 | Intron | XP_011523445.1 | ||||
XM_017024968.1 | Intron | XP_016880457.1 | ||||
XM_017024969.1 | Intron | XP_016880458.1 |
SP2-AS1 - SP2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |