Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATCCGGTGGACGGTTCTGTGGTT[C/T]GCGATTTTGAGCACAGGCCCAAAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
WDR88 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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WDR88 - WD repeat domain 88 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173479.3 | 484 | Missense Mutation | CGC,TGC | R,C 138 | NP_775750.3 | |
XM_011526449.2 | 484 | Missense Mutation | CGC,TGC | R,C 138 | XP_011524751.1 | |
XM_011526450.2 | 484 | Missense Mutation | CGC,TGC | R,C 138 | XP_011524752.1 | |
XM_017026282.1 | 484 | Missense Mutation | CGC,TGC | R,C 138 | XP_016881771.1 | |
XM_017026283.1 | 484 | Missense Mutation | CGC,TGC | R,C 138 | XP_016881772.1 |