SLC45A2 c.529G>T ;(p.E177*)

Variant ID: 5-33982374-C-A

NM_016180.3(SLC45A2):c.529G>T;(p.E177*)

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:

Comprehensive analysis of spectral distribution of a large cohort of Chinese patients with non-syndromic oculocutaneous albinism facilitates genetic diagnosis.

Pigment Cell & Melanoma Research
Zhong, Zilin Z; Gu, Li L; Zheng, Xiujie X; Ma, Nengjun N; Wu, Zehua Z; Duan, Juan J; Zhang, Jun J; Chen, Jianjun J
Publication Date: 2019-09

Variant appearance in text: SLC45A2: 529G>T
PubMed Link: 31077556
Variant Present in the following documents:
  • Main text
  • PCMR-32-672.pdf
View BVdb publication page