Variant #0001038784 (NC_000011.9:g.764389C>T, NM_006755.1:c.937C>T (TALDO1))

Chromosome 11
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.764389C>T
DNA change (hg38) -
Published as TALDO1(NM_006755.2):c.937C>T (p.R313C)
ISCN -
DB-ID PDDC1_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
TALDO1 NM_006755.1 ?/. - c.937C>T r.(?) p.(Arg313Cys)
PDDC1 NM_182612.2 ?/. - c.*6508G>A r.(=) p.(=)


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