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TCCCAGGCTCCAGAGATCCTCCCAC[C/G]TCAGCCACCTATGTGGCTGGTATTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610610 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GINS3 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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GINS3 - GINS complex subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126129.1 | 483 | Missense Mutation | CCT,CGT | P,R 92 | NP_001119601.1 | |
NM_001126130.1 | 483 | Intron | NP_001119602.1 | |||
NM_022770.3 | 483 | Intron | NP_073607.2 |