Variant #0000338140 (NC_000019.9:g.46088097C>T, NM_001017989.2:c.-75G>A (OPA3))

Chromosome 19
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.46088097C>T
DNA change (hg38) g.45584839C>T
Published as -
ISCN -
DB-ID OPA3_000002 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPA3 NM_001017989.2 -/. - c.-75G>A r.(?) p.(=)
GPR4 NM_005282.2 -/. - c.*5939G>A r.(=) p.(=)
OPA3 NM_025136.3 -/. - c.-75G>A r.(?) p.(=)


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