Variant #0000128313 (NC_000011.9:g.111958644del, SDHD(NM_003002.2):c.116del)

Individual ID 00079439
Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111958644del
DNA change (hg38) g.112087920del
Published as -
ISCN -
DB-ID SDHD_000167
Variant remarks -
Reference PubMed: Persu
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Jean-Pierre Bayley
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHD NM_003002.2 ?/. 2 c.116del r.(?) p.(Pro39Leufs*47) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000079512 DNA SEQ - - SDHD 1 Jean-Pierre Bayley