COL3A1 c.2410G>A ;(p.G804S)

Variant ID: 2-189867042-G-A

NM_000090.3(COL3A1):c.2410G>A;(p.G804S)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: COL3A1: 2410G>A; Gly804Ser
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome

Balkan Medical Journal
Forghani, Irman I
Publication Date: 2019-01-01

Variant appearance in text: COL3A1: 2410G>A; Gly804Ser
PubMed Link: 30063214
Variant Present in the following documents:
  • Main text
  • BMJ-36-12.pdf
View BVdb publication page



Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.

Plos One
LaDuca, Holly H; Farwell, Kelly D KD; Vuong, Huy H; Lu, Hsiao-Mei HM; Mu, Wenbo W; Shahmirzadi, Layla L; Tang, Sha S; Chen, Jefferey J; Bhide, Shruti S; Chao, Elizabeth C EC
Publication Date: 2017

Variant appearance in text: COL3A1: 2410G>A
PubMed Link: 28152038
Variant Present in the following documents:
  • Main text
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: COL3A1: G804S
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 3
View BVdb publication page



Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report.

Journal Of Medical Case Reports
Kashizaki, Fumihiro F; Hatamochi, Atsushi A; Kamiya, Kazunori K; Yoshizu, Akira A; Okamoto, Hiroaki H
Publication Date: 2013-02-01

Variant appearance in text: COL3A1: 2410G>A; G804S
PubMed Link: 23374456
Variant Present in the following documents:
  • Main text
  • 1752-1947-7-35.pdf
View BVdb publication page



Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Nucleic Acids Research
Ryu, Gil-Mi GM; Song, Pamela P; Kim, Kyu-Won KW; Oh, Kyung-Soo KS; Park, Keun-Joon KJ; Kim, Jong Hun JH
Publication Date: 2009-03

Variant appearance in text: COL3A1: G804S
PubMed Link: 19139070
Variant Present in the following documents:
  • gkn1008_nar-01723-s-2008-File009.xls, sheet 2
  • gkn1008_nar-01723-s-2008-File011.xls, sheet 2
View BVdb publication page