Variant #0000116373 (NC_000005.9:g.223595A>G, NC_000005.9(NM_004168.2):c.64-2A>G (SDHA))
Chromosome |
5 |
Allele |
Maternal (inferred) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.223595A>G |
DNA change (hg38) |
g.223480A>G |
Published as |
- |
ISCN |
- |
DB-ID |
SDHA_000022 See all 4 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Herma Renkema |
Database submission license |
No license selected |
Created by |
Herma Renkema |
Date created |
2013-08-19 17:12:56 +02:00 (CEST) |
Date last edited |
2024-02-13 17:19:38 +01:00 (CET) |

Variant on transcripts
Screenings
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