Variant #0000863431 (NC_000014.8:g.103396588_103396595dup, NM_006035.3:c.*3460_*3467dup (CDC42BPB))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103396588_103396595dup
DNA change (hg38) -
Published as AMN(NM_030943.3):c.1093_1100dupGTGGCGGC (p.A368Wfs*49)
ISCN -
DB-ID AMN_000036
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
CDC42BPB NM_006035.3 +/. - c.*3460_*3467dup r.(=) p.(=)
AMN NM_030943.3 +/. - c.1093_1100dup r.(?) p.(Ala368Trpfs*49)


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