GAA c.149_207del ;(p.E50Gfs*26)

Variant ID: 17-78078533-GGAGGAGACTCACCCAGCTCACCAGCAGGGAGCCAGCAGACCAGGGCCCCGGGATGCCCA-G

NM_000152.3(GAA):c.149_207del;(p.E50Gfs*26)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease.

Molecular Genetics And Metabolism
Mori, Mari M; Haskell, Gloria G; Kazi, Zoheb Z; Zhu, Xiaolin X; DeArmey, Stephanie M SM; Goldstein, Jennifer L JL; Bali, Deeksha D; Rehder, Catherine C; Cirulli, Elizabeth T ET; Kishnani, Priya S PS
Publication Date: 2017-12

Variant appearance in text: GAA: 148_859del
PubMed Link: 29122469
Variant Present in the following documents:
  • Main text
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