EGR1 c.36_38del ;(p.P13del)

Variant ID: 5-137801484-TCCC-T

NM_001964.2(EGR1):c.36_38del;(p.P13del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq.

Npj Genomic Medicine
Koster, R R; Brandão, R D RD; Tserpelis, D D; van Roozendaal, C E P CEP; van Oosterhoud, C N CN; Claes, K B M KBM; Paulussen, A D C ADC; Sinnema, M M; Vreeburg, M M; van der Schoot, V V; Stumpel, C T R M CTRM; Broen, M P G MPG; Spruijt, L L; Jongmans, M C J MCJ; Lesnik Oberstein, S A J SAJ; Plomp, A S AS; Misra-Isrie, M M; Duijkers, F A FA; Louwers, M J MJ; Szklarczyk, R R; Derks, K W J KWJ; Brunner, H G HG; van den Wijngaard, A A; van Geel, M M; Blok, M J MJ
Publication Date: 2021-11-15

Variant appearance in text: 225: 36_38del
PubMed Link: 34782607
Variant Present in the following documents:
  • 41525_2021_258_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page