FBN1 c.7002T>C ;(p.N2334=)

Variant ID: 15-48719966-A-G

NM_000138.4(FBN1):c.7002T>C;(p.N2334=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genomic and Transcriptomic Characterization of Relapsed SCLC Through Rapid Research Autopsy.

Jto Clinical And Research Reports
Chen, Hui-Zi HZ; Bonneville, Russell R; Paruchuri, Anoosha A; Reeser, Julie W JW; Wing, Michele R MR; Samorodnitsky, Eric E; Krook, Melanie A MA; Smith, Amy M AM; Dao, Thuy T; Miya, Jharna J; Wang, Walter W; Yu, Lianbo L; Freud, Aharon G AG; Allenby, Patricia P; Cole, Sharon S; Otterson, Gregory G; Shields, Peter P; Carbone, David P DP; Roychowdhury, Sameek S
Publication Date: 2021-04

Variant appearance in text: FBN1: N2334N
PubMed Link: 34590014
Variant Present in the following documents:
  • mmc6.xlsx, sheet 13
  • mmc6.xlsx, sheet 12
  • mmc13.xlsx, sheet 7
  • mmc6.xlsx, sheet 8
  • mmc6.xlsx, sheet 14
  • mmc6.xlsx, sheet 6
  • mmc6.xlsx, sheet 7
  • mmc6.xlsx, sheet 3
  • mmc6.xlsx, sheet 5
  • mmc6.xlsx, sheet 4
  • mmc6.xlsx, sheet 15
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