Variant #0000866263 (NC_000019.9:g.54649680C>T, NM_014516.3:c.738C>T (CNOT3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54649680C>T
DNA change (hg38) -
Published as CNOT3(NM_014516.4):c.738C>T (p.H246=)
ISCN -
DB-ID CNOT3_000035
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNOT3 NM_014516.3 -?/. - c.738C>T r.(?) p.(His246=)
LENG1 NM_024316.1 -?/. - c.*9779G>A r.(=) p.(=)


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