Variant #0001043164 (NC_000019.9:g.54665991C>T, NM_014516.3:c.*6846C>T (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.54665991C>T
DNA change (hg38) -
Published as TMC4(NM_144686.4):c.1533G>A (p.(Leu511=))
ISCN -
DB-ID CNOT3_000052
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC4 NM_001145303.1 ?/. - c.1551G>A r.(?) p.(=)
CNOT3 NM_014516.3 ?/. - c.*6846C>T r.(=) p.(=)
LENG1 NM_024316.1 ?/. - c.-2558G>A r.(?) p.(=)


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