Variant #0000888222 (NC_000008.10:g.145107999G>A, NM_017570.3:c.2905C>T (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.145107999G>A
DNA change (hg38) -
Published as OPLAH(NM_017570.4):c.2905C>T (p.R969C), OPLAH(NM_017570.5):c.2905C>T (p.R969C)
ISCN -
DB-ID OPLAH_000003 See all 2 reported entries
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) 0.00063 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 2022-11-01 13:01:21 +01:00 (CET)
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.2905C>T r.(?) p.(Arg969Cys)
SMPD5 XM_001714032.3 ?/. - c.*1892G>A r.(=) p.(=)


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