Variant #0000963587 (NC_000005.9:g.218598G>A, NC_000005.9(NM_004168.2):c.63+65G>A (SDHA))

Chromosome 5
Allele Unknown
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.218598G>A
DNA change (hg38) -
Published as SDHA(NM_004168.4):c.63+65G>A
ISCN -
DB-ID CCDC127_000002
Variant remarks VKGL data sharing initiative Nederland; Variant no longer found in the VKGL dataset for this center.
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2026-01-21 10:44:29 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SDHA NM_004168.2 -/. - c.63+65G>A r.(=) p.(=)
CCDC127 NM_145265.2 -/. - c.-401C>T r.(?) p.(=)


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