Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGAAGCTGCCGGTGCGCACGGAG[A/C]CCGCCATGCCTCGCCTTGGCGCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610610 | ||||||||||||||||||||
Literature Links: |
GINS3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
GINS3 - GINS complex subunit 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126129.1 | 320 | Missense Mutation | ACC,CCC | T,P 38 | NP_001119601.1 | |
NM_001126130.1 | 320 | Missense Mutation | ACC,CCC | T,P 38 | NP_001119602.1 | |
NM_022770.3 | 320 | Missense Mutation | ACC,CCC | T,P 38 | NP_073607.2 |