Variant #0001041226 (NC_000016.9:g.58577439_58577442del, NC_000016.9(NM_016284.4):c.4434+70_4434+73del (CNOT1))

Chromosome 16
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.58577439_58577442del
DNA change (hg38) -
Published as CNOT1(NM_206999.3):c.4504_4507del (p.(Val1502Ilefs*18))
ISCN -
DB-ID CNOT1_000091
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 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.4434+70_4434+73del r.(=) p.(=)
SETD6 NM_024860.2 -?/. - c.*24506_*24509del r.(=) p.(=)


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