Variant #0000725888 (NC_000016.9:g.58577328dup, NC_000016.9(NM_016284.4):c.4434+195dup (CNOT1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58577328dup
DNA change (hg38) -
Published as CNOT1(NM_206999.2):c.4629dupT (p.L1544Sfs*22)
ISCN -
DB-ID CNOT1_000042
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 2021-02-08 18:36:18 +01:00 (CET)
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+195dup r.(=) p.(=)
SETD6 NM_024860.2 -/. - c.*24395dup r.(?) p.(=)


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