Variant #0000533489 (NC_000008.10:g.105393468_105393471del, NM_001385.2:c.1515_1518del (DPYS))

Chromosome 8
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.105393468_105393471del
DNA change (hg38) g.104381240_104381243del
Published as DPYS(NM_001385.2):c.1515_1518delAAAA (p.E507Mfs*57)
ISCN -
DB-ID DPYS_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) 0.00029 View details
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 15:12:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPYS NM_001385.2 ?/. - c.1515_1518del r.(?) p.(Glu507MetfsTer57)


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