Variant #0000064201 (NC_000001.10:g.17380491G>A, SDHB(NM_003000.2):c.24C>T)

Individual ID 00037006
Chromosome 1
Allele Parent #1
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.17380491G>A
DNA change (hg38) g.17053996G>A
Published as -
ISCN -
DB-ID SDHB_000011 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs148738139
Origin Germline
Segregation -
Frequency MAF A=0,007
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00437 View details
Owner Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHB NM_003000.2 -/. - c.24C>T r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000037076 DNA SEQ - - SDHB 1 Andreas Laner