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GGAAAGAATCACTTTTATTTTGGAT[C/T]GTTCTTTATGGAACGAGTATGTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600618 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ETV6 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
|
ETV6 - ETS variant 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001987.4 | Intron | NP_001978.1 | ||||
XM_011520607.2 | Intron | XP_011518909.1 | ||||
XM_011520608.2 | Intron | XP_011518910.1 | ||||
XM_011520609.2 | Intron | XP_011518911.1 | ||||
XM_011520611.2 | Intron | XP_011518913.1 | ||||
XM_011520612.2 | Intron | XP_011518914.1 | ||||
XM_017018990.1 | Intron | XP_016874479.1 | ||||
XM_017018991.1 | Intron | XP_016874480.1 |