Variant #0000011688 (NC_000001.11:g.161314406A>G, SDHC(NM_003001.3):c.1A>G)

Individual ID 00005285
Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.161314406A>G
Reference -
DB-ID chr1_000010
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Instituto Nacional del Cancer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Options




Variant on transcripts


Gene     
AscendingTranscript     
Affects function     
Exon     
DNA change (cDNA)     
Protein     
Zygosity     
Co_ocurrence     
RNA change     
Review status     
SDHC NM_003001.3 +/+ 1 c.1A>G p.Met1Val Hetero no r.? -



Screenings


AscendingScreening ID     
Template     
Technique     
Lab     
Remarks     
Date of test     
Type of test     
Genes screened     
Variants found     
Owner     
0000009469 DNA SEQ-NG Laboratorio Central ACD, AIP, AKT1, APC, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA1_5UTR, BRCA2, BRCA2_5UTR, BRIP1, CASR, CDH1, CDKN1B, CDKN2A, CDK4, CTRC, DDB2, DICER1, DIS3L2, EPCAM, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, FAM175A, FANCA, FANCB, FANCC, FANCI, FANCL, FANCM, FANCF, FANCE, FLCN, FH, GALNT12, GATA2, GREM1, HOXB13, KIT, KIF1B, LZTR1, MAX, MEN1, MET, MLH1, MRE11A, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NSD1, NTHL1, PALB2, PDGFRA, PIK3CA, PMS2, POLE, POT1, PRKAR1A, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RECQL4, RET, RHBDF2, RINT1, RUNX1, SDHA, SDHB, SDHC, SDHD, SDHAF2, SLX4, SMAD4, SMARCA4, SMARCB1, SMARCE1, SPINK1, SPRED1, SRY, SUFU, TERT, TERF2IP, TMEM127, TSC1, TSC2, TP53, VHL, WT1, XPA, XPC, XRCC2, ZMYM3. 28-jan-2025 Multigenetic panel - 2 Norma Rossi - Sanatorio Allende

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