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TAATACCAAGACTATCATCGAAGAC[A/T]AATTAGAAAATAGCAATCAACAGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601337 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RFX3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
RFX3 - regulatory factor X3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282116.1 | Intron | NP_001269045.1 | ||||
NM_001282117.1 | Intron | NP_001269046.1 | ||||
NM_002919.3 | Intron | NP_002910.1 | ||||
NM_134428.2 | Intron | NP_602304.1 | ||||
XM_006716840.1 | Intron | XP_006716903.1 | ||||
XM_006716843.1 | Intron | XP_006716906.1 | ||||
XM_006716844.1 | Intron | XP_006716907.1 | ||||
XM_006716845.2 | Intron | XP_006716908.1 | ||||
XM_006716847.3 | Intron | XP_006716910.1 | ||||
XM_011517998.1 | Intron | XP_011516300.1 | ||||
XM_011517999.1 | Intron | XP_011516301.1 | ||||
XM_011518000.1 | Intron | XP_011516302.1 | ||||
XM_011518001.1 | Intron | XP_011516303.1 | ||||
XM_017015000.1 | Intron | XP_016870489.1 | ||||
XM_017015001.1 | Intron | XP_016870490.1 | ||||
XM_017015002.1 | Intron | XP_016870491.1 |