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EGFR T263P
genetic variant
T263P
THR263PRO
In more languages
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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/995
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/995
genomic start
55221743
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
genomic end
55221743
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
biological variant of
EGFR
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
positive therapeutic predictor for
erlotinib
determination method
CIViC evidence level D
rating
CIViC 3-star trust rating
medical condition treated
glioma
1 reference
curator
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/evidence/4187
stated in
Epidermal growth factor receptor activation in glioblastoma through novel missense mutations in the extracellular domain
Identifiers
CIViC variant ID
995
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
dbSNP Reference SNP number
rs1057519829
1 reference
stated in
CIViC database
HGVS nomenclature
NM_005228.4:c.787A>C
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
NP_005219.2:p.Thr263Pro
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
NC_000007.13:g.55221743A>C
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
ENST00000275493.2:c.787A>C
1 reference
stated in
CIViC database
retrieved
28 March 2022
reference URL
https://civic.genome.wustl.edu/links/variants/995
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