Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGTGGCTCCATGCTGGGGCTGG[A/C]ACACGCCTGCGACAGTGAGGAATTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
RFX8 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 |
RFX8 - RFX family member 8, lacking RFX DNA binding domain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145664.1 | 1246 | Missense Mutation | GCC,TCC | A,S 373 | NP_001139136.1 | |
XM_011511771.2 | 1246 | Missense Mutation | GCC,TCC | A,S 449 | XP_011510073.1 | |
XM_011511772.1 | 1246 | Missense Mutation | GCC,TCC | A,S 444 | XP_011510074.1 | |
XM_011511773.1 | 1246 | Missense Mutation | GCC,TCC | A,S 343 | XP_011510075.1 | |
XM_011511776.1 | 1246 | Missense Mutation | GCC,TCC | A,S 277 | XP_011510078.1 | |
XM_011511777.1 | 1246 | Missense Mutation | GCC,TCC | A,S 277 | XP_011510079.1 | |
XM_011511778.1 | 1246 | Missense Mutation | GCC,TCC | A,S 277 | XP_011510080.1 | |
XM_017004851.1 | 1246 | Missense Mutation | GCC,TCC | A,S 486 | XP_016860340.1 | |
XM_017004852.1 | 1246 | Missense Mutation | GCC,TCC | A,S 415 | XP_016860341.1 | |
XM_017004853.1 | 1246 | Intron | XP_016860342.1 | |||
XM_017004854.1 | 1246 | Intron | XP_016860343.1 |