Variant #0000534171 (NC_000008.10:g.145112401C>T, NM_017570.3:c.1372G>A (OPLAH))

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.145112401C>T
DNA change (hg38) g.144057498C>T
Published as OPLAH(NM_017570.4):c.1372G>A (p.V458M)
ISCN -
DB-ID OPLAH_000012
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) 0.00015 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 18:59:24 +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.1372G>A r.(?) p.(Val458Met)
SMPD5 XM_001714032.3 ?/. - c.*6294C>T r.(=) p.(=)


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