Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGTCCATGGCAGTGCTCCAGTCCA[C/T]GGTGACCACAGGGGCTCGGTGGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616303 | ||||||||||||||||||||
Literature Links: |
WDR91 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 |
WDR91 - WD repeat domain 91 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014149.3 | 1751 | Missense Mutation | ATG,GTG | M,V 717 | NP_054868.3 | |
XM_011516083.2 | 1751 | Missense Mutation | ATG,GTG | M,V 762 | XP_011514385.1 | |
XM_011516086.2 | 1751 | Missense Mutation | ATG,GTG | M,V 736 | XP_011514388.1 | |
XM_017012070.1 | 1751 | Missense Mutation | ATG,GTG | M,V 743 | XP_016867559.1 | |
XM_017012071.1 | 1751 | Missense Mutation | ATG,GTG | M,V 519 | XP_016867560.1 | |
XM_017012072.1 | 1751 | Missense Mutation | ATG,GTG | M,V 474 | XP_016867561.1 |