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TTTAGAGTTTGCAGAGGGCTAGAGT[C/T]GGCATATTCTGTTCCTAAGGTTGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605255 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ETV7 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
|
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
|
ETV7 - ETS variant 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001207035.1 | Intron | NP_001193964.1 | ||||
NM_001207036.1 | Intron | NP_001193965.1 | ||||
NM_001207037.1 | Intron | NP_001193966.1 | ||||
NM_001207038.1 | Intron | NP_001193967.1 | ||||
NM_001207039.1 | Intron | NP_001193968.1 | ||||
NM_001207040.1 | Intron | NP_001193969.1 | ||||
NM_001207041.1 | Intron | NP_001193970.1 | ||||
NM_016135.3 | Intron | NP_057219.1 | ||||
XM_011514659.1 | Intron | XP_011512961.1 |