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TTCCATAAGGCTGTCCAATTCAGGT[C/T]TTCTGTTATCTTTTGAAGTATGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613602 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WDR35 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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WDR35 - WD repeat domain 35 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006657.1 | 2168 | Missense Mutation | AAA,AGA | K,R 1123 | NP_001006658.1 | |
NM_020779.3 | 2168 | Missense Mutation | AAA,AGA | K,R 1112 | NP_065830.2 | |
XM_011533007.2 | 2168 | Missense Mutation | AAA,AGA | K,R 688 | XP_011531309.1 |