OCA2 c.79G>A ;(p.G27R)

Variant ID: 15-28326942-C-T

NM_000275.2(OCA2):c.79G>A;(p.G27R)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Genetic variants in African-American and Hispanic patients with breast cancer.

Oncology Letters
Dutta, Pranabananda P; Keung, Man Y MY; Wu, Yanyuan Y; Vadgama, Jaydutt V JV
Publication Date: 2023-02

Variant appearance in text: OCA2: 79G>A; G27R
PubMed Link: 36644153
Variant Present in the following documents:
  • Supplementary_Data5.xlsx, sheet 1
View BVdb publication page



Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene.

Frontiers In Genetics
Marek-Yagel, Dina D; Abudi-Sinreich, Shachar S; Macarov, Michal M; Veber, Alvit A; Shalva, Nechama N; Philosoph, Amit Mary AM; Pode-Shakked, Ben B; Malicdan, May Christine V MCV; Anikster, Yair Y
Publication Date: 2022

Variant appearance in text: OCA2: G27R
PubMed Link: 36046236
Variant Present in the following documents:
  • Main text
  • fgene-13-936064.pdf
View BVdb publication page



A novel porcine model reproduces human oculocutaneous albinism type II.

Cell Discovery
Zhang, Ying Y; Hong, Qianlong Q; Cao, Chunwei C; Yang, Lizhu L; Li, Yongshun Y; Hai, Tang T; Zhang, Hongyong H; Zhou, Qi Q; Sui, Ruifang R; Zhao, Jianguo J
Publication Date: 2019

Variant appearance in text: OCA2: G27R
PubMed Link: 31636960
Variant Present in the following documents:
  • Main text
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: N/A
PubMed Link: 26659599
Variant Present in the following documents:
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: OCA2: G27R
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 2
View BVdb publication page



DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.

Human Mutation
Simeonov, Dimitre R DR; Wang, Xinjing X; Wang, Chen C; Sergeev, Yuri Y; Dolinska, Monika M; Bower, Matthew M; Fischer, Roxanne R; Winer, David D; Dubrovsky, Genia G; Balog, Joan Z JZ; Huizing, Marjan M; Hart, Rachel R; Zein, Wadih M WM; Gahl, William A WA; Brooks, Brian P BP; Adams, David R DR
Publication Date: 2013-06

Variant appearance in text: OCA2: 79G>A
PubMed Link: 23504663
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type.

The Journal Of Investigative Dermatology
Hutton, Saunie M SM; Spritz, Richard A RA
Publication Date: 2008-10

Variant appearance in text: OCA2: 79G>A; G27R
PubMed Link: 18463683
Variant Present in the following documents:
  • Main text
View BVdb publication page