Variant #0000337531 (NC_000005.9:g.223915_223920del, NC_000005.9(NM_004168.2):c.150+232_150+237del (SDHA))

Chromosome 5
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.223915_223920del
DNA change (hg38) g.223800_223805del
Published as SDHA:NM_004168.2:c.150+232_150+237del (?)
ISCN -
DB-ID SDHA_000116
Variant remarks VKGL data sharing initiative Nederland; Variant no longer found in the VKGL dataset for this center.
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 2026-01-21 10:44:59 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SDHA NM_004168.2 -/. - c.150+232_150+237del r.(=) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.