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TGTCATCGGTCATCTCTAGAAACTG[C/T]GCGTAGACATCTCGGATGCACTCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609226 | ||||||||||||||||||||
Literature Links: |
WDR45B 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 |
WDR45B - WD repeat domain 45B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019613.3 | 1197 | Silent Mutation | GCA,GCG | A,A 334 | NP_062559.2 | |
XM_005256377.4 | 1197 | Intron | XP_005256434.1 | |||
XM_017024862.1 | 1197 | Intron | XP_016880351.1 | |||
XM_017024863.1 | 1197 | Intron | XP_016880352.1 |