SYNJ1 c.2050T>G ;(p.C684G)

Variant ID: 21-34038348-A-C

NM_203446.2(SYNJ1):c.2050T>G;(p.C684G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: SYNJ1: C723G; rs751110096
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Computational analysis of functional SNPs in Alzheimer's disease-associated endocytosis genes.

Peerj
Tey, Han Jieh HJ; Ng, Chong Han CH
Publication Date: 2019

Variant appearance in text: SYNJ1: C723G; rs751110096
PubMed Link: 31592138
Variant Present in the following documents:
  • Main text
  • peerj-07-7667.pdf
View BVdb publication page