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TCTTTGGCGGGGATGGAGGTTTCCC[C/T]GCAGGAAATGAACCAGGACTGAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 116896 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUX1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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
|
CUX1 - cut like homeobox 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001202543.1 | Intron | NP_001189472.1 | ||||
NM_001202544.2 | Intron | NP_001189473.1 | ||||
NM_001202545.2 | Intron | NP_001189474.1 | ||||
NM_001202546.2 | Intron | NP_001189475.1 | ||||
NM_001913.4 | Intron | NP_001904.2 | ||||
NM_181500.3 | Intron | NP_852477.1 | ||||
NM_181552.3 | Intron | NP_853530.2 | ||||
XM_005250150.2 | Intron | XP_005250207.1 | ||||
XM_005250151.2 | Intron | XP_005250208.1 | ||||
XM_005250154.3 | Intron | XP_005250211.1 | ||||
XM_006715854.2 | Intron | XP_006715917.1 | ||||
XM_006715855.1 | Intron | XP_006715918.1 | ||||
XM_011515823.2 | Intron | XP_011514125.1 | ||||
XM_011515825.1 | Intron | XP_011514127.1 | ||||
XM_017011759.1 | Intron | XP_016867248.1 | ||||
XM_017011760.1 | Intron | XP_016867249.1 |