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CCCCAGGGGACCCAGTGGGGAGAGG[A/C]ATCTGAAAATGTTTACCCAAAGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 167409 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PAX2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PAX2 - paired box 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000278.4 | Intron | NP_000269.3 | ||||
NM_001304569.1 | Intron | NP_001291498.1 | ||||
NM_003987.4 | Intron | NP_003978.3 | ||||
NM_003988.4 | Intron | NP_003979.2 | ||||
NM_003989.4 | Intron | NP_003980.3 | ||||
NM_003990.4 | Intron | NP_003981.3 | ||||
XM_017016281.1 | Intron | XP_016871770.1 | ||||
XM_017016282.1 | Intron | XP_016871771.1 | ||||
XM_017016283.1 | Intron | XP_016871772.1 | ||||
XM_017016284.1 | Intron | XP_016871773.1 | ||||
XM_017016285.1 | Intron | XP_016871774.1 | ||||
XM_017016286.1 | Intron | XP_016871775.1 | ||||
XM_017016287.1 | Intron | XP_016871776.1 | ||||
XM_017016288.1 | Intron | XP_016871777.1 | ||||
XM_017016289.1 | Intron | XP_016871778.1 |