Variant #0000528091 (NC_000006.11:g.24302087G>A, NC_000006.11(NM_016356.3):c.426-13C>T (DCDC2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24302087G>A
DNA change (hg38) g.24301859G>A
Published as DCDC2(NM_016356.5):c.426-13C>T
ISCN -
DB-ID KAAG1_000008
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) 0.99591 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 2019-07-18 18:22:55 +02:00 (CEST)
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.426-13C>T r.(=) p.(=)
KAAG1 NM_181337.3 -/. - c.-55781G>A r.(?) p.(=)


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