Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGTGCGCCAGTTCACACTCCGG[A/G]TCAGAGTTCCTGGCCCGGTGCACCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602580 MIM: 616528 | ||||||||||||||||||||
Literature Links: |
GOLGA2 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 |
GOLGA2 - golgin A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004486.4 | 145 | Intron | NP_004477.3 | |||
XM_005251930.1 | 145 | Intron | XP_005251987.1 | |||
XM_005251931.1 | 145 | Intron | XP_005251988.1 | |||
XM_005251932.1 | 145 | Intron | XP_005251989.1 |
SWI5 - SWI5 homologous recombination repair protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040011.1 | 145 | Missense Mutation | ATC,GTC | I,V 49 | NP_001035100.1 | |
NM_001318089.1 | 145 | Missense Mutation | ATC,GTC | I,V 49 | NP_001305018.1 | |
NM_001318092.1 | 145 | Intron | NP_001305021.1 | |||
XM_011518652.2 | 145 | Missense Mutation | ATC,GTC | I,V 49 | XP_011516954.1 |