The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
[Disclaimer]
- Gene obtained from curated document aligns with the Allele Registry but not with ClinVar data
- No CSPEC computed assertion could be determined for this classification!
Variant: NM_000249.4(MLH1):c.2040C>T (p.Cys680=)
- Curation Version - 1.0
- Curation History
- JSON LD for Version 1.0
CA008297
90010 (ClinVar)
Gene: MLH1
Condition: Lynch syndrome
Inheritance Mode: Autosomal dominant inheritance
UUID: 70a1d4a4-791a-494a-a70e-fc4c558d31d5
Approved on: 2024-09-19
Published on: 2024-10-11
HGVS expressions
NM_000249.4:c.2040C>T
NM_000249.4(MLH1):c.2040C>T (p.Cys680=)
NC_000003.12:g.37048954C>T
CM000665.2:g.37048954C>T
NC_000003.11:g.37090445C>T
CM000665.1:g.37090445C>T
NC_000003.10:g.37065449C>T
NG_007109.2:g.60605C>T
ENST00000413740.2:c.1668-1532C>T
ENST00000429117.6:c.1746C>T
ENST00000450420.6:c.1559-1532C>T
ENST00000456676.7:c.1896+1271C>T
ENST00000492474.6:c.1317C>T
ENST00000616768.6:c.1947C>T
ENST00000673673.2:c.1875C>T
ENST00000231790.8:c.2040C>T
ENST00000413212.2:c.*958C>T
ENST00000432299.6:c.*1872C>T
ENST00000447829.6:c.*1151C>T
ENST00000539477.6:c.1317C>T
ENST00000616768.5:c.984C>T
ENST00000673673.1:c.1828C>T
ENST00000673741.1:n.1074C>T
ENST00000673889.1:n.1422C>T
ENST00000673897.1:c.*1832C>T
ENST00000673899.1:c.1308C>T
ENST00000673947.1:c.*2180C>T
ENST00000673972.1:c.*1918C>T
ENST00000674019.1:c.1317C>T
ENST00000674111.1:c.*269C>T
ENST00000674125.1:n.751C>T
ENST00000231790.6:c.2040C>T
ENST00000413740.1:c.291-1532C>T
ENST00000435176.5:c.1746C>T
ENST00000450420.5:c.182-1532C>T
ENST00000455445.6:c.1317C>T
ENST00000456676.6:c.1871+1271C>T
ENST00000458205.6:c.1317C>T
ENST00000536378.5:c.1317C>T
ENST00000539477.5:c.1317C>T
NM_000249.3:c.2040C>T
NM_001167617.1:c.1746C>T
NM_001167618.1:c.1317C>T
NM_001167619.1:c.1317C>T
NM_001258271.1:c.1896+1271C>T
NM_001258273.1:c.1317C>T
NM_001258274.1:c.1317C>T
NM_001167617.2:c.1746C>T
NM_001167618.2:c.1317C>T
NM_001167619.2:c.1317C>T
NM_001258274.2:c.1317C>T
NM_001354615.1:c.1317C>T
NM_001354616.1:c.1317C>T
NM_001354617.1:c.1317C>T
NM_001354618.1:c.1317C>T
NM_001354619.1:c.1317C>T
NM_001354620.1:c.1746C>T
NM_001354621.1:c.1017C>T
NM_001354622.1:c.1017C>T
NM_001354623.1:c.1017C>T
NM_001354624.1:c.966C>T
NM_001354625.1:c.966C>T
NM_001354626.1:c.966C>T
NM_001354627.1:c.966C>T
NM_001354628.1:c.1947C>T
NM_001354629.1:c.1941C>T
NM_001354630.1:c.1875C>T
NM_001167617.3:c.1746C>T
NM_001167618.3:c.1317C>T
NM_001167619.3:c.1317C>T
NM_001258271.2:c.1896+1271C>T
NM_001258273.2:c.1317C>T
NM_001258274.3:c.1317C>T
NM_001354615.2:c.1317C>T
NM_001354616.2:c.1317C>T
NM_001354617.2:c.1317C>T
NM_001354618.2:c.1317C>T
NM_001354619.2:c.1317C>T
NM_001354620.2:c.1746C>T
NM_001354621.2:c.1017C>T
NM_001354622.2:c.1017C>T
NM_001354623.2:c.1017C>T
NM_001354624.2:c.966C>T
NM_001354625.2:c.966C>T
NM_001354626.2:c.966C>T
NM_001354627.2:c.966C>T
NM_001354628.2:c.1947C>T
NM_001354629.2:c.1941C>T
NM_001354630.2:c.1875C>T
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Evidence submitted by expert panel
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