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GCGGACCTCCGGCCTGGGGAGACCA[C/T]GGGTGCTAACTCTGCTGGCGGGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
28 submissions
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Phenotype: |
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Literature Links: |
TMCC2 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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TMCC2 - transmembrane and coiled-coil domain family 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242925.1 | 771 | Intron | NP_001229854.1 | |||
NM_001297611.1 | 771 | Intron | NP_001284540.1 | |||
NM_001297613.1 | 771 | Intron | NP_001284542.1 | |||
NM_014858.3 | 771 | Missense Mutation | ACG,ATG | T,M 39 | NP_055673.2 | |
XM_005245684.1 | 771 | Intron | XP_005245741.1 | |||
XM_005245685.4 | 771 | Intron | XP_005245742.1 | |||
XM_005245686.3 | 771 | Missense Mutation | ACG,ATG | T,M 39 | XP_005245743.1 | |
XM_017003000.1 | 771 | Intron | XP_016858489.1 |