Variant #0000967388 (NC_000014.8:g.103396910_103396926del, NM_006035.3:c.*3125_*3141del (CDC42BPB))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103396910_103396926del
DNA change (hg38) -
Published as AMN(NM_030943.3):c.1258-5_1269delCGCAGCCCCTGCCGCGG
ISCN -
DB-ID AMN_000044
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.*3125_*3141del r.(=) p.(=)
AMN NM_030943.3 +?/. - c.1258-3_1271del r.spl? p.?


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