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GCAGGATGAGCATTAATACTACTTC[C/G]AGAATCTATAAAATCCCAATGCTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ANKRD42 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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ANKRD42 - ankyrin repeat domain 42 | ||||||
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There are no transcripts associated with this gene. |
CCDC90B - coiled-coil domain containing 90B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286116.1 | 1513 | Missense Mutation | TCG,TGG | S,W 244 | NP_001273045.1 | |
NM_001286117.1 | 1513 | Missense Mutation | TCG,TGG | S,W 152 | NP_001273046.1 | |
NM_001286118.1 | 1513 | Missense Mutation | TCG,TGG | S,W 155 | NP_001273047.1 | |
NM_001286119.1 | 1513 | Missense Mutation | TCG,TGG | S,W 155 | NP_001273048.1 | |
NM_001286120.1 | 1513 | Missense Mutation | TCG,TGG | S,W 138 | NP_001273049.1 | |
NM_021825.4 | 1513 | Missense Mutation | TCG,TGG | S,W 253 | NP_068597.2 | |
XM_005274154.2 | 1513 | Missense Mutation | TCG,TGG | S,W 155 | XP_005274211.1 | |
XM_005274156.3 | 1513 | Missense Mutation | TCG,TGG | S,W 155 | XP_005274213.1 | |
XM_005274159.3 | 1513 | Missense Mutation | TCG,TGG | S,W 152 | XP_005274216.1 | |
XM_017018103.1 | 1513 | Missense Mutation | TCG,TGG | S,W 155 | XP_016873592.1 | |
XM_017018104.1 | 1513 | Missense Mutation | TCG,TGG | S,W 152 | XP_016873593.1 |