Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACACTGCGTGCCACGGACCTCACTC[C/T]GGCAGTGGCTGCAGTACACGCCGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
WDR59 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
WDR59 - WD repeat domain 59 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324171.1 | 2561 | Intron | NP_001311100.1 | |||
NM_001324172.1 | 2561 | Intron | NP_001311101.1 | |||
NM_030581.3 | 2561 | Missense Mutation | CAG,CGG | Q,R 906 | NP_085058.3 | |
XM_005256146.3 | 2561 | Missense Mutation | CAG,CGG | Q,R 925 | XP_005256203.1 | |
XM_011523331.2 | 2561 | Missense Mutation | CAG,CGG | Q,R 618 | XP_011521633.1 | |
XM_011523332.2 | 2561 | Missense Mutation | CAG,CGG | Q,R 604 | XP_011521634.1 | |
XM_017023667.1 | 2561 | Missense Mutation | CAG,CGG | Q,R 654 | XP_016879156.1 | |
XM_017023668.1 | 2561 | Missense Mutation | CAG,CGG | Q,R 654 | XP_016879157.1 | |
XM_017023669.1 | 2561 | Missense Mutation | CAG,CGG | Q,R 618 | XP_016879158.1 | |
XM_017023670.1 | 2561 | Missense Mutation | CAG,CGG | Q,R 604 | XP_016879159.1 |