Variant #0000803525 (NC_000008.10:g.145110796_145110797del, NM_017570.3:c.2142_2143del (OPLAH))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145110796_145110797del
DNA change (hg38) -
Published as OPLAH(NM_017570.4):c.2142_2143delAG (p.D716Hfs*34)
ISCN -
DB-ID OPLAH_000020
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) 2.0E-5 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 2021-09-17 14:40:49 +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     
OPLAH NM_017570.3 +?/. - c.2142_2143del r.(?) p.(Asp716Hisfs*34)
SMPD5 XM_001714032.3 +?/. - c.*4689_*4690del r.(=) p.(=)


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