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TTACTTCCAAGGAAACCAGAATCAC[A/G]GAATTCTAAAAAGATGTGGCATTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615462 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WDR60 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
|
WDR60 - WD repeat domain 60 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018051.4 | Intron | NP_060521.4 | ||||
XM_005249549.1 | Intron | XP_005249606.1 | ||||
XM_006716041.2 | Intron | XP_006716104.1 | ||||
XM_011516367.1 | Intron | XP_011514669.1 | ||||
XM_011516368.2 | Intron | XP_011514670.1 | ||||
XM_011516369.2 | Intron | XP_011514671.1 | ||||
XM_017012381.1 | Intron | XP_016867870.1 | ||||
XM_017012382.1 | Intron | XP_016867871.1 | ||||
XM_017012383.1 | Intron | XP_016867872.1 | ||||
XM_017012384.1 | Intron | XP_016867873.1 | ||||
XM_017012385.1 | Intron | XP_016867874.1 | ||||
XM_017012386.1 | Intron | XP_016867875.1 | ||||
XM_017012387.1 | Intron | XP_016867876.1 | ||||
XM_017012388.1 | Intron | XP_016867877.1 |