Variant #0000337511 (NC_000005.9:g.218444C>G, SDHA(NM_004168.2):c.-27C>G)

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.218444C>G
DNA change (hg38) g.218329C>G
Published as -
ISCN -
DB-ID SDHA_000113
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license No license selected
Created by VKGL-NL_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHA NM_004168.2 -?/. - c.-27C>G r.(?) p.(=) - -
CCDC127 NM_145265.2 -?/. - c.-247G>C r.(?) p.(=) - -