Variant #0001041227 (NC_000016.9:g.58577546T>C, NM_016284.4:c.4399A>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.58577546T>C
DNA change (hg38) -
Published as CNOT1(NM_016284.5):c.4399A>G (p.(Thr1467Ala))
ISCN -
DB-ID CNOT1_000092
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
CNOT1 NM_016284.4 ?/. - c.4399A>G r.(?) p.(Thr1467Ala)
SETD6 NM_024860.2 ?/. - c.*24613T>C r.(=) p.(=)


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