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EGFR Y801H
genetic variant
Y801H
Y748H
Y756H
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No label defined
No description defined
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Statements
instance of
missense mutation
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
genomic start
55249103
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
genomic end
55249103
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
biological variant of
EGFR
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
positive therapeutic predictor for
erlotinib
determination method or standard
CIViC evidence level D
rating
CIViC 3-star trust rating
medical condition treated
cancer
1 reference
curator
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/evidence/4659
stated in
Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma
Identifiers
CIViC variant ID
1575
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
dbSNP Reference SNP number
rs757642107
1 reference
stated in
CIViC database
HGVS nomenclature
ENST00000275493.2:c.2401T>C
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/1575
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