Variant #0000692885 (NC_000019.9:g.54655963G>C, NM_014516.3:c.1606G>C (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.54655963G>C
DNA change (hg38) -
Published as CNOT3(NM_014516.4):c.1606G>C (p.A536P)
ISCN -
DB-ID CNOT3_000030
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.1606G>C r.(?) p.(Ala536Pro)
LENG1 NM_024316.1 ?/. - c.*3496C>G r.(=) p.(=)


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