Variant #0001002459 (NC_000016.9:g.58621715T>C, NM_016284.4:c.278A>G (CNOT1))

Chromosome 16
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.58621715T>C
DNA change (hg38) -
Published as CNOT1(NM_016284.4):c.278A>G (p.(Tyr93Cys))
ISCN -
DB-ID CNOT1_000087
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNOT1 NM_016284.4 ?/. - c.278A>G r.(?) p.(Tyr93Cys)
SETD6 NM_024860.2 ?/. - c.*68782T>C r.(=) p.(=)


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