Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCGGACCTCCGGCCTGGGGAGACC[A/G]CGGGTGCTAACTCTGCTGGCGGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 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 |
---|---|---|
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 |
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 | 770 | Intron | NP_001229854.1 | |||
NM_001297611.1 | 770 | Intron | NP_001284540.1 | |||
NM_001297613.1 | 770 | Intron | NP_001284542.1 | |||
NM_014858.3 | 770 | Missense Mutation | ACG,GCG | T,A 39 | NP_055673.2 | |
XM_005245684.1 | 770 | Intron | XP_005245741.1 | |||
XM_005245685.4 | 770 | Intron | XP_005245742.1 | |||
XM_005245686.3 | 770 | Missense Mutation | ACG,GCG | T,A 39 | XP_005245743.1 | |
XM_017003000.1 | 770 | Intron | XP_016858489.1 |