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GAATAATCATTCCCTTGCTTTTCCT[A/C]GTTTTTTTGTTTGTTTGTTTTGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 165080 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ERG PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ERG - ERG, ETS transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136154.1 | Intron | NP_001129626.1 | ||||
NM_001136155.1 | Intron | NP_001129627.1 | ||||
NM_001243428.1 | Intron | NP_001230357.1 | ||||
NM_001243429.1 | Intron | NP_001230358.1 | ||||
NM_001243432.2 | Intron | NP_001230361.1 | ||||
NM_001291391.1 | Intron | NP_001278320.1 | ||||
NM_004449.4 | Intron | NP_004440.1 | ||||
NM_182918.3 | Intron | NP_891548.1 | ||||
XM_011529486.2 | Intron | XP_011527788.1 | ||||
XM_011529487.2 | Intron | XP_011527789.1 | ||||
XM_017028287.1 | Intron | XP_016883776.1 | ||||
XM_017028288.1 | Intron | XP_016883777.1 | ||||
XM_017028289.1 | Intron | XP_016883778.1 |