Annotation Detail
Information
- Associated Genes
- KCNH2
- Associated Variants
-
KCNH2 p.Gly628Arg (p.G628R)
(
ENST00000262186.10,
ENST00000330883.9,
ENST00000713701.1,
ENST00000713710.1 )
KCNH2 p.Gly628Arg (p.G628R) ( ENST00000262186.10, ENST00000330883.9, ENST00000713701.1, ENST00000713710.1 ) - Source Database
- ClinVar
- Description
- NM_000238.4(KCNH2):c.1882G>C (p.Gly628Arg) AND Cardiovascular phenotype
- ClinVar Allele ID
- 197250
- ClinVar RefSeq Alternation Syntax
- NM_001406756.1:c.1594G>C
- ClinVar RefSeq Alternation Syntax
- NM_000238.4:c.1882G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406757.1:c.1582G>C
- ClinVar RefSeq Alternation Syntax
- NM_001204798.2:c.862G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406753.1:c.1594G>C
- ClinVar RefSeq Alternation Syntax
- NM_172056.3:c.1882G>C
- ClinVar RefSeq Alternation Syntax
- NM_172057.3:c.862G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406755.1:c.1705G>C
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2018-07-26
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002408792
- Observed Origin Sample
- germline
Drugs