Annotation Detail
Information
- Associated Genes
- SDHC
- Associated Variants
-
SDHC p.Gly75Asp (p.G75D)
(
ENST00000392169.6,
ENST00000714065.1,
ENST00000342751.8,
ENST00000432287.6,
ENST00000714066.1,
ENST00000367975.7,
ENST00000714063.1,
ENST00000515731.2,
ENST00000513009.5,
ENST00000714064.1 )
SDHC p.Gly75Asp (p.G75D) ( ENST00000342751.8, ENST00000367975.7, ENST00000392169.6, ENST00000432287.6, ENST00000513009.5, ENST00000515731.2, ENST00000714063.1, ENST00000714064.1, ENST00000714065.1, ENST00000714066.1 ) - Associated Disease
- Carney triad
- Source Database
- ClinVar
- Description
- NM_003001.5(SDHC):c.224G>A (p.Gly75Asp) AND Carney triad
- ClinVar Allele ID
- 187698
- ClinVar RefSeq Alternation Syntax
- NM_001407117.1:c.167G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407121.1:c.167G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407116.1:c.167G>A
- ClinVar RefSeq Alternation Syntax
- NM_003001.5:c.224G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407115.1:c.344G>A
- ClinVar RefSeq Alternation Syntax
- NM_001035511.3:c.224G>A
- ClinVar RefSeq Alternation Syntax
- NM_001035513.3:c.65G>A
- ClinVar RefSeq Alternation Syntax
- NM_001278172.3:c.122G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407119.1:c.113G>A
- ClinVar RefSeq Alternation Syntax
- NM_001035512.3:c.122G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407118.1:c.122G>A
- ClinVar RefSeq Alternation Syntax
- NM_001407120.1:c.113G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000170332
- ClinVar Disease
- Carney triad
- Observed Origin Sample
- germline
Drugs