Variant #0001035642 (NC_000006.11:g.24667079C>A, NM_016614.2:c.12G>T (TDP2))

Chromosome 6
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.24667079C>A
DNA change (hg38) -
Published as TDP2(NM_016614.3):c.12G>T (p.(Gly4=))
ISCN -
DB-ID ACOT13_000005
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) 2.0E-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     
TDP2 NM_016614.2 ?/. - c.12G>T r.(?) p.(=)
ACOT13 NM_018473.3 ?/. - c.-413C>A r.(?) p.(=)
C6orf62 NM_030939.4 ?/. - c.*39286G>T r.(=) p.(=)


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