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Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603179 MIM: 190990 | |||||||||||||||||||||||
Literature Links: |
CA9 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
CA9 - carbonic anhydrase 9 | ||||||
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There are no transcripts associated with this gene. |
TPM2 - tropomyosin 2 (beta) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301226.1 | 1056 | Intron | NP_001288155.1 | |||
NM_001301227.1 | 1056 | Missense Mutation | AAA,GAA | K,E 273 | NP_001288156.1 | |
NM_003289.3 | 1056 | Missense Mutation | AAA,GAA | K,E 273 | NP_003280.2 | |
NM_213674.1 | 1056 | Intron | NP_998839.1 | |||
XM_017015087.1 | 1056 | UTR 3 | XP_016870576.1 | |||
XM_017015088.1 | 1056 | Intron | XP_016870577.1 | |||
XM_017015089.1 | 1056 | Intron | XP_016870578.1 | |||
XM_017015090.1 | 1056 | Missense Mutation | AAA,GAA | K,E 273 | XP_016870579.1 | |
XM_017015091.1 | 1056 | Missense Mutation | AAA,GAA | K,E 273 | XP_016870580.1 | |
XM_017015092.1 | 1056 | UTR 3 | XP_016870581.1 | |||
XM_017015093.1 | 1056 | Intron | XP_016870582.1 |
Set Membership: |
HapMap |