Variant #0000116373 (NC_000005.9:g.223595A>G, NC_000005.9(NM_004168.2):c.64-2A>G (SDHA))

Chromosome 5
Allele Maternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.223595A>G
DNA change (hg38) g.223480A>G
Published as -
ISCN -
DB-ID SDHA_000022 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Herma Renkema
Database submission license No license selected
Created by Herma Renkema
Date created 2013-08-19 17:12:56 +02:00 (CEST)
Date last edited 2024-02-13 17:19:38 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHA NM_004168.2 +/? 1i c.64-2A>G r.[64_73del, r.63_64ins64-54_64-1;64-2a>g] p.(=) - -



Screenings

Stop! No screenings found!


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.