Variant #0000865976 (NC_000019.9:g.18899085_18899088dup, NM_000095.2:c.908_911dup (COMP))

Chromosome 19
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.18899085_18899088dup
DNA change (hg38) -
Published as COMP(NM_000095.2):c.911_912insTGGA (p.(Arg305GlyfsTer21))
ISCN -
DB-ID COMP_000186
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +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     
COMP NM_000095.2 +/. - c.908_911dup r.(?) p.(Arg305Glyfs*21)


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