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TGAGATTCATCCGGGCTGTATAATT[A/G]GAGGGCAGGTTGTTCATTCCCAAAC
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
RFX7 - regulatory factor X7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022841.5 | 5054 | Silent Mutation | TCC,TCT | S,S 1275 | NP_073752.5 | |
XM_005254603.3 | 5054 | Silent Mutation | TCC,TCT | S,S 1275 | XP_005254660.2 | |
XM_011521925.2 | 5054 | Silent Mutation | TCC,TCT | S,S 1178 | XP_011520227.1 | |
XM_017022506.1 | 5054 | Silent Mutation | TCC,TCT | S,S 1275 | XP_016877995.1 | |
XM_017022507.1 | 5054 | Silent Mutation | TCC,TCT | S,S 1178 | XP_016877996.1 | |
XM_017022508.1 | 5054 | Silent Mutation | TCC,TCT | S,S 1178 | XP_016877997.1 |