Variant #0000304793 (NC_000008.10:g.145112495G>A, NM_017570.3:c.1278C>T (OPLAH))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145112495G>A
DNA change (hg38) g.144057592G>A
Published as OPLAH(NM_017570.4):c.1278C>T (p.A426=)
ISCN -
DB-ID OPLAH_000007
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-24 18:59:37 +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.1278C>T r.(?) p.(Ala426=)
SMPD5 XM_001714032.3 -?/. - c.*6388G>A r.(=) p.(=)


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