Variant #0000533689 (NC_000008.10:g.119123227_119123230del, NM_000127.2:c.56_59del (EXT1))

Chromosome 8
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.119123227_119123230del
DNA change (hg38) g.118110988_118110991del
Published as EXT1(NM_000127.2):c.56_59delTTTT (p.L19Rfs*116)
ISCN -
DB-ID EXT1_000784
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-24 15:24:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXT1 NM_000127.2 +/. - c.56_59del r.(?) p.(Leu19ArgfsTer116)


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