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TCTAGGTCATCTCCCTCTGGGGTCC[A/G]GTAGGAGACCTGAGCCTTCTGCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300970 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MORC4 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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MORC4 - MORC family CW-type zinc finger 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085354.2 | 2797 | Intron | NP_001078823.1 | |||
NM_024657.4 | 2797 | Missense Mutation | CGG,TGG | R,W 878 | NP_078933.3 | |
XM_005262190.3 | 2797 | Missense Mutation | CGG,TGG | R,W 786 | XP_005262247.1 | |
XM_006724691.2 | 2797 | Missense Mutation | CGG,TGG | R,W 756 | XP_006724754.1 | |
XM_011531027.2 | 2797 | Missense Mutation | CGG,TGG | R,W 701 | XP_011529329.1 | |
XM_017029844.1 | 2797 | Intron | XP_016885333.1 |