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AATGTAGTGGTCAGTTTTCTCTTGC[A/G]GTCGTCAGCCTGAACATAACATCCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131550 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EGFR 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)
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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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EGFR - epidermal growth factor receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005228.3 | 1563 | Silent Mutation | GCA,GCG | A,A 439 | NP_005219.2 | |
NM_201282.1 | 1563 | Silent Mutation | GCA,GCG | A,A 439 | NP_958439.1 | |
NM_201283.1 | 1563 | Intron | NP_958440.1 | |||
NM_201284.1 | 1563 | Silent Mutation | GCA,GCG | A,A 439 | NP_958441.1 |
Set Membership: |
HapMap |