Variant #0001000257 (NC_000012.11:g.57921739del, NM_006400.4:c.*2740del (DCTN2))

Chromosome 12
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.57921739del
DNA change (hg38) -
Published as MBD6(NM_052897.3):c.2345delG (p.(Gly782fs))
ISCN -
DB-ID DCTN2_000010
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 2024-08-28 13:16:32 +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     
DCTN2 NM_006400.4 ?/. - c.*2740del r.(?) p.(=)
MBD6 NM_052897.3 ?/. - c.2345del r.(?) p.(Gly782Glufs*13)


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