chr3:37042456:T>C Detail (hg19) (MLH1)

Go to:

Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
Genome browser

Information

Genome

Assembly	Position
hg19	chr3:37,042,456-37,042,456
hg38	chr3:37,000,965-37,000,965 View the variant detail on this assembly version.

HGVS

MLH1

Type	Transcript	Protein
RefSeq	NM_000249.3:c.218T>C	NP_000240.1:p.Leu73Pro
	NM_001167617.1:c.-72T>C
	NM_001167618.1:c.-506T>C
	NM_001258271.1:c.218T>C	NP_001245200.1:p.Leu73Pro
	NM_001258274.1:c.-506T>C
	NM_001258273.1:c.-506T>C
	NM_001167619.1:c.-414T>C
Ensemble	ENST00000231790.8:c.218T>C	ENST00000231790.8:p.Leu73Pro
	ENST00000435176.5:c.-72T>C
	ENST00000441265.6:c.-506T>C
	ENST00000450420.6:c.218T>C	ENST00000450420.6:p.Leu73Pro
	ENST00000455445.6:c.-506T>C
	ENST00000456676.7:c.218T>C	ENST00000456676.7:p.Leu73Pro
	ENST00000458205.6:c.-506T>C
	ENST00000466900.6:c.-612T>C
	ENST00000485889.2:c.-506T>C
	ENST00000492474.6:c.-506T>C
	ENST00000536378.5:c.-506T>C
	ENST00000539477.6:c.-414T>C
	ENST00000616768.6:c.218T>C	ENST00000616768.6:p.Leu73Pro
	ENST00000673673.2:c.218T>C	ENST00000673673.2:p.Leu73Pro
	ENST00000673715.1:c.218T>C	ENST00000673715.1:p.Leu73Pro
	ENST00000673899.1:c.218T>C	ENST00000673899.1:p.Leu73Pro
	ENST00000673990.2:c.-712T>C
	ENST00000674019.1:c.-506T>C
	ENST00000713802.1:c.208-3436T>C

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Conflicting classifications of pathogenicity
Review star
Show details

Links

MLH1

Type	Database	ID	Link
Gene	MIM	120436	OMIM
	HGNC	7127	HGNC
	Ensembl	ENSG00000076242	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Uncertain significance	2021-04-17	criteria provided, single submitter	Hereditary nonpolyposis colorectal neoplasms	germline	Detail
Likely pathogenic	2023-03-31	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Likely pathogenic	2023-07-12	criteria provided, single submitter	Colorectal cancer, hereditary nonpolyposis, type 2	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.492	Turcot syndrome (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000249.4(MLH1):c.218T>C (p.Leu73Pro) AND Hereditary nonpolyposis colorectal neoplasms	ClinVar	Detail
NM_000249.4(MLH1):c.218T>C (p.Leu73Pro) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000249.4(MLH1):c.218T>C (p.Leu73Pro) AND Colorectal cancer, hereditary nonpolyposis, type 2	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs397514684 dbSNP
Genome: hg19
Position: chr3:37,042,456-37,042,456
Variant Type: snv
Reference Allele: T
Alternative Allele: C

Genome browser