Variant #0000866264 (NC_000019.9:g.54650371C>A, NM_014516.3:c.872C>A (CNOT3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.54650371C>A
DNA change (hg38) -
Published as CNOT3(NM_014516.4):c.872C>A (p.S291Y)
ISCN -
DB-ID CNOT3_000036
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNOT3 NM_014516.3 ?/. - c.872C>A r.(?) p.(Ser291Tyr)
LENG1 NM_024316.1 ?/. - c.*9088G>T r.(=) p.(=)


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