Annotation Detail
Information
- Associated Genes
- KCNQ1 KCNQ1OT1
- Associated Variants
-
KCNQ1 c.1514+8160A>G
(
ENST00000646564.2,
ENST00000335475.6,
ENST00000713725.1,
ENST00000496887.7,
ENST00000155840.12 )
KCNQ1 c.1514+8160A>G ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.1514+8160A>G AND not provided
- ClinVar Allele ID
- 1247677
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.1514+8160A>G
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.1133+8160A>G
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.1418+8160A>G
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.1244+8160A>G
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.974+8160A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-02-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001666044
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs