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Search Thermo Fisher Scientific
CCAGGCAGCAGCCCACCTGCAGTGA[C/T]AGGACCCGCGTCCGCATCCGCACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 603319 | ||||||||||||||||||||
Literature Links: |
ANXA9 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 |
ANXA9 - annexin A9 | ||||||
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There are no transcripts associated with this gene. |
FAM63A - family with sequence similarity 63 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040217.2 | 2000 | Silent Mutation | CTA,CTG | L,L 298 | NP_001035307.1 | |
NM_001163258.1 | 2000 | Silent Mutation | CTA,CTG | L,L 488 | NP_001156730.1 | |
NM_001163259.1 | 2000 | Silent Mutation | CTA,CTG | L,L 345 | NP_001156731.1 | |
NM_001163260.1 | 2000 | Silent Mutation | CTA,CTG | L,L 298 | NP_001156732.1 | |
NM_001319998.1 | 2000 | Silent Mutation | CTA,CTG | L,L 440 | NP_001306927.1 | |
NM_018379.4 | 2000 | Silent Mutation | CTA,CTG | L,L 440 | NP_060849.2 | |
XM_005245321.3 | 2000 | Silent Mutation | CTA,CTG | L,L 441 | XP_005245378.1 | |
XM_005245325.3 | 2000 | Silent Mutation | CTA,CTG | L,L 299 | XP_005245382.1 | |
XM_005245327.3 | 2000 | Silent Mutation | CTA,CTG | L,L 275 | XP_005245384.1 | |
XM_005245328.3 | 2000 | Silent Mutation | CTA,CTG | L,L 274 | XP_005245385.1 | |
XM_011509757.2 | 2000 | Silent Mutation | CTA,CTG | L,L 432 | XP_011508059.1 | |
XM_011509759.2 | 2000 | Silent Mutation | CTA,CTG | L,L 387 | XP_011508061.1 | |
XM_017001770.1 | 2000 | Silent Mutation | CTA,CTG | L,L 440 | XP_016857259.1 | |
XM_017001771.1 | 2000 | Silent Mutation | CTA,CTG | L,L 440 | XP_016857260.1 | |
XM_017001772.1 | 2000 | Silent Mutation | CTA,CTG | L,L 440 | XP_016857261.1 | |
XM_017001773.1 | 2000 | Silent Mutation | CTA,CTG | L,L 431 | XP_016857262.1 | |
XM_017001774.1 | 2000 | Silent Mutation | CTA,CTG | L,L 431 | XP_016857263.1 | |
XM_017001775.1 | 2000 | Silent Mutation | CTA,CTG | L,L 387 | XP_016857264.1 | |
XM_017001776.1 | 2000 | Silent Mutation | CTA,CTG | L,L 378 | XP_016857265.1 | |
XM_017001777.1 | 2000 | Silent Mutation | CTA,CTG | L,L 488 | XP_016857266.1 |