Variant #0000524683 (NC_000005.9:g.146795397_146795398del, NM_001197294.1:c.695_696del (DPYSL3))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.146795397_146795398del
DNA change (hg38) g.147415834_147415835del
Published as DPYSL3(NM_001197294.2):c.695_696delAG (p.E232Gfs*3)
ISCN -
DB-ID DPYSL3_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 18:10:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPYSL3 NM_001197294.1 ?/. - c.695_696del r.(?) p.(Glu232GlyfsTer3)


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