Variant #0000269843 (NC_000001.10:g.32669918G>A, NM_024296.3:c.463G>A (CCDC28B))

Chromosome 1
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.32669918G>A
DNA change (hg38) g.32204317G>A
Published as CCDC28B(NM_024296.4):c.463G>A (p.G155R)
ISCN -
DB-ID CCDC28B_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) 0.00563 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCDC2B NM_001099434.1 -?/. - c.-4777G>A r.(?) p.(=)
IQCC NM_018134.2 -?/. - c.-1365G>A r.(?) p.(=)
CCDC28B NM_024296.3 -?/. - c.463G>A r.(?) p.(Gly155Arg)


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