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CCAACAGAAAGAACGGACTGTAGCA[A/G]CATGCCCTCCCTGAAGGCTAGTCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
WDR89 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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WDR89 - WD repeat domain 89 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008726.2 | 1724 | Missense Mutation | GCT,GTT | A,V 321 | NP_001008726.1 | |
NM_001258272.1 | 1724 | Missense Mutation | GCT,GTT | A,V 321 | NP_001245201.1 | |
NM_080666.3 | 1724 | Missense Mutation | GCT,GTT | A,V 321 | NP_542397.1 | |
XM_011536383.2 | 1724 | Missense Mutation | GCT,GTT | A,V 359 | XP_011534685.1 | |
XM_011536385.2 | 1724 | Missense Mutation | GCT,GTT | A,V 321 | XP_011534687.1 |