Variant #0000504016 (NC_000001.10:g.161310406T>C, SDHC(NM_003001.3):c.202T>C)

Chromosome 1
Allele Unknown
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.161310406T>C
DNA change (hg38) g.161340616T>C
Published as SDHC(NM_003001.3):c.202T>C (p.S68P)
ISCN -
DB-ID SDHC_000083 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_VUmc
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
SDHC NM_003001.3 ?/. - c.202T>C r.(?) p.(Ser68Pro) - -