Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGACTGTGTCTCTGTGGGTCGCCG[C/T]GTGGGCCGGCGTGACCCCCCGGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602581 | ||||||||||||||||||||
Literature Links: |
GOLGA3 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 |
GOLGA3 - golgin A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172557.1 | 2603 | Intron | NP_001166028.1 | |||
NM_005895.3 | 2603 | Missense Mutation | CAC,CGC | H,R 1480 | NP_005886.2 | |
XM_005266164.4 | 2603 | Missense Mutation | CAC,CGC | H,R 1440 | XP_005266221.1 | |
XM_005266167.4 | 2603 | Missense Mutation | CAC,CGC | H,R 1289 | XP_005266224.1 | |
XM_006719736.3 | 2603 | Missense Mutation | CAC,CGC | H,R 1480 | XP_006719799.1 | |
XM_006719737.3 | 2603 | Missense Mutation | CAC,CGC | H,R 1480 | XP_006719800.1 | |
XM_011534793.2 | 2603 | Missense Mutation | CAC,CGC | H,R 1389 | XP_011533095.1 | |
XM_011534794.2 | 2603 | Missense Mutation | CAC,CGC | H,R 832 | XP_011533096.1 |