Variant #0000528089 (NC_000006.11:g.24291203T>C, NM_016356.3:c.661A>G (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.24291203T>C
DNA change (hg38) g.24290975T>C
Published as DCDC2(NM_016356.5):c.661A>G (p.S221G)
ISCN -
DB-ID KAAG1_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) 0.65432 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCDC2 NM_016356.3 -/. - c.661A>G r.(?) p.(Ser221Gly)
KAAG1 NM_181337.3 -/. - c.-66665T>C r.(?) p.(=)


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