NSF c.268_269delinsGC ;(p.Q90A)

Variant ID: 17-44714771-CA-GC

NM_006178.3(NSF):c.268_269delinsGC;(p.Q90A)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

K2P channel C-type gating involves asymmetric selectivity filter order-disorder transitions.

Science Advances
Lolicato, Marco M; Natale, Andrew M AM; Abderemane-Ali, Fayal F; Crottès, David D; Capponi, Sara S; Duman, Ramona R; Wagner, Armin A; Rosenberg, John M JM; Grabe, Michael M; Minor, Daniel L DL
Publication Date: 2020-10

Variant appearance in text: NSF: Q90A
PubMed Link: 33127683
Variant Present in the following documents:
  • Main text
  • abc9174.pdf
View BVdb publication page


K2P channel C-type gating involves asymmetric selectivity filter order-disorder transitions.

Science Advances
Lolicato, Marco M; Natale, Andrew M AM; Abderemane-Ali, Fayal F; Crottès, David D; Capponi, Sara S; Duman, Ramona R; Wagner, Armin A; Rosenberg, John M JM; Grabe, Michael M; Minor, Daniel L DL
Publication Date: 2020-10

Variant appearance in text: NSF: Q90A
PubMed Link: 33127683
Variant Present in the following documents:
  • Main text
  • abc9174.pdf
View BVdb publication page