Genomic variant #0000116727

Individual ID 00072848
Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.(161310446_161326466)_(161326631_161332118)del
DNA change (hg38) -
Published as Deletion Exon 5
ISCN -
DB-ID SDHC_000031
Variant remarks -
Reference PubMed: Neumann
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Jean-Pierre Bayley




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHC NM_003001.3 ?/+ 4i_5i c.(241+1_242-1)_(405+1_406-1)del - r.spl? p.? - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000073005 DNA SEQ - - SDHC 1 Jean-Pierre Bayley