(Q29938506)

English

EGFR L747_P753delinsS

genetic variant

L747_P753DELINSS
RS121913438

In more languages

default for all languages

No label defined

No description defined

Statements

Inframe Deletion

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

human chromosome 7

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

55242470

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

55242487

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

biological variant of

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

positive therapeutic predictor for

determination method or standard

CIViC evidence level C

CIViC 3-star trust rating

medical condition treated

pancreatic adenocarcinoma

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/evidence/6005

EGFR Exon 19 Deletion in Pancreatic Adenocarcinoma Responds to Erlotinib, Followed by T790M-Mediated Resistance

Identifiers

CIViC variant ID

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/1012

dbSNP Reference SNP number

1 reference

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q29938506&oldid=2014804784"