Annotation Detail
Information
- Associated Genes
- MSH6
- Associated Variants
-
MSH6 p.Thr767Ser (p.T767S)
(
ENST00000455383.6,
ENST00000411819.2,
ENST00000234420.11,
ENST00000420813.6,
ENST00000405808.5,
ENST00000540021.6,
ENST00000652107.1,
ENST00000673637.1,
ENST00000700000.1,
ENST00000700002.1,
ENST00000700004.2 )
MSH6 p.Thr767Ser (p.T767S) ( ENST00000234420.11, ENST00000411819.2, ENST00000420813.6, ENST00000455383.6, ENST00000540021.6, ENST00000652107.1, ENST00000673637.1, ENST00000700000.1, ENST00000700002.1, ENST00000700004.2, ENST00000405808.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000179.3(MSH6):c.2300C>G (p.Thr767Ser) AND not provided
- ClinVar Allele ID
- 405897
- ClinVar RefSeq Alternation Syntax
- NM_001281493.2:c.1394C>G
- ClinVar RefSeq Alternation Syntax
- NM_001281494.2:c.1394C>G
- ClinVar RefSeq Alternation Syntax
- NM_000179.3:c.2300C>G
- ClinVar RefSeq Alternation Syntax
- NM_001281492.2:c.1910C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-11-22
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001284514
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs