Variant #0000565173 (NC_000018.9:g.57115306_57115307insA, NM_133459.3:c.683_684insT (CCBE1))

Chromosome 18
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.57115306_57115307insA
DNA change (hg38) g.59448074_59448075insA
Published as CCBE1(NM_133459.3):c.683_684insT (p.(Leu229fs)), CCBE1(NM_133459.4):c.683_684insT (p.L229Pfs*8)
ISCN -
DB-ID CCBE1_000014 See all 5 reported entries
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) 5.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCBE1 NM_133459.3 +/. - c.683_684insT r.(?) p.(Leu229ProfsTer8)


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