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GGTAGAAATAGTTGCTTGACCATTC[C/T]GCAGGTTCTTCAGAGATTTCTGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 311030 | ||||||||||||||||||||
Literature Links: |
MCF2 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 |
MCF2 - MCF.2 cell line derived transforming sequence | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099855.1 | 3127 | Silent Mutation | GCA,GCG | A,A 953 | NP_001093325.1 | |
NM_001171876.1 | 3127 | Silent Mutation | GCA,GCG | A,A 969 | NP_001165347.1 | |
NM_001171877.1 | 3127 | Intron | NP_001165348.1 | |||
NM_001171878.1 | 3127 | Intron | NP_001165349.1 | |||
NM_001171879.1 | 3127 | Silent Mutation | GCA,GCG | A,A 909 | NP_001165350.1 | |
NM_005369.4 | 3127 | Silent Mutation | GCA,GCG | A,A 893 | NP_005360.3 | |
XM_005262413.4 | 3127 | Silent Mutation | GCA,GCG | A,A 1012 | XP_005262470.1 | |
XM_011531339.2 | 3127 | Silent Mutation | GCA,GCG | A,A 969 | XP_011529641.1 | |
XM_017029529.1 | 3127 | Silent Mutation | GCA,GCG | A,A 1012 | XP_016885018.1 | |
XM_017029530.1 | 3127 | Intron | XP_016885019.1 | |||
XM_017029531.1 | 3127 | Silent Mutation | GCA,GCG | A,A 969 | XP_016885020.1 | |
XM_017029532.1 | 3127 | Silent Mutation | GCA,GCG | A,A 909 | XP_016885021.1 |