Variant #0000678326 (NC_000008.10:g.145107390C>T, NM_017570.3:c.3265G>A (OPLAH))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145107390C>T
DNA change (hg38) -
Published as OPLAH(NM_017570.5):c.3265G>A (p.V1089I)
ISCN -
DB-ID OPLAH_000008
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) 0.00952 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPLAH NM_017570.3 -/. - c.3265G>A r.(?) p.(Val1089Ile)
SMPD5 XM_001714032.3 -/. - c.*1283C>T r.(=) p.(=)


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