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MYOC c.987G>C ;(p.V329=)
Variant ID: 1-171605593-C-G
NM_000261.1(
MYOC
):c.987G>C;(p.V329=)
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:
Genetic modifiers of long-term survival in sickle cell anemia.
Clinical And Translational Medicine
Wonkam, Ambroise A; Chimusa, Emile R ER; Mnika, Khuthala K; Pule, Gift Dineo GD; Ngo Bitoungui, Valentina Josiane VJ; Mulder, Nicola N; Shriner, Daniel D; Rotimi, Charles N CN; Adeyemo, Adebowale A
Publication Date: 2020-08
Variant appearance in text: MYOC: V329V
PubMed Link:
32898326
Variant Present in the following documents:
CTM2-10-e152-s001.pdf
View BVdb publication page