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GGTCCCTAAAGAAAGCCAAATGACA[C/G]TAGCTATTCAGGGACTCAAAACCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612660 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RFX7 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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RFX7 - regulatory factor X7 | ||||||
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There are no transcripts associated with this gene. |
TEX9 - testis expressed 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286449.1 | Intron | NP_001273378.1 | ||||
NM_198524.2 | Intron | NP_940926.1 | ||||
XM_005254359.4 | Intron | XP_005254416.1 | ||||
XM_005254361.3 | Intron | XP_005254418.1 | ||||
XM_011521530.2 | Intron | XP_011519832.1 | ||||
XM_017022160.1 | Intron | XP_016877649.1 | ||||
XM_017022161.1 | Intron | XP_016877650.1 | ||||
XM_017022162.1 | Intron | XP_016877651.1 | ||||
XM_017022163.1 | Intron | XP_016877652.1 | ||||
XM_017022164.1 | Intron | XP_016877653.1 | ||||
XM_017022166.1 | Intron | XP_016877655.1 | ||||
XM_017022167.1 | Intron | XP_016877656.1 |