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Search Thermo Fisher Scientific
CCCGGCTGGGGAAGCCCTTCCAGCT[C/G]CTGGTTCTGCTTCAGTTCCCTCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611508 MIM: 610056 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAMTA2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CAMTA2 - calmodulin binding transcription activator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171166.1 | 4355 | Missense Mutation | CAG,GAG | Q,E 1186 | NP_001164637.1 | |
NM_001171167.1 | 4355 | Missense Mutation | GCA,GGA | A,G 1213 | NP_001164638.1 | |
NM_001171168.1 | 4355 | Missense Mutation | CAG,GAG | Q,E 1190 | NP_001164639.1 | |
NM_015099.3 | 4355 | Missense Mutation | CAG,GAG | Q,E 1191 | NP_055914.2 | |
XM_006721478.3 | 4355 | Missense Mutation | CAG,GAG | Q,E 1196 | XP_006721541.1 | |
XM_006721481.3 | 4355 | Missense Mutation | CAG,GAG | Q,E 1167 | XP_006721544.1 | |
XM_006721482.3 | 4355 | Missense Mutation | CAG,GAG | Q,E 1004 | XP_006721545.1 | |
XM_011523746.2 | 4355 | Missense Mutation | CAG,GAG | Q,E 1219 | XP_011522048.1 | |
XM_011523747.2 | 4355 | Missense Mutation | CAG,GAG | Q,E 1214 | XP_011522049.1 | |
XM_011523748.2 | 4355 | Missense Mutation | CAG,GAG | Q,E 1212 | XP_011522050.1 | |
XM_011523749.2 | 4355 | Missense Mutation | CAG,GAG | Q,E 1207 | XP_011522051.1 |
MIR6864 - microRNA 6864 | ||||||
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There are no transcripts associated with this gene. |
MIR6865 - microRNA 6865 | ||||||
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There are no transcripts associated with this gene. |
SPAG7 - sperm associated antigen 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004890.2 | 4355 | Intron | NP_004881.2 | |||
XM_006721600.2 | 4355 | Intron | XP_006721663.1 |