Variant #0000655544 (NC_000006.11:g.24178840G>A, NM_016356.3:c.1044C>T (DCDC2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24178840G>A
DNA change (hg38) g.24178612G>A
Published as DCDC2(NM_016356.5):c.1044C>T (p.D348=)
ISCN -
DB-ID KAAG1_000011
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) 0.00384 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCDC2 NM_016356.3 -?/. - c.1044C>T r.(?) p.(Asp348=)
KAAG1 NM_181337.3 -?/. - c.-179028G>A r.(?) p.(=)


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