chr3:37025999:C> Detail (hg38) (MLH1)

Information

Genome

Assembly Position
hg19 chr3:37,067,490-37,067,490 
hg38 chr3:37,025,999-37,025,999

HGVS

Type Transcript Protein
RefSeq NM_000249.3:c.1401delC NP_000240.1:p.Ser467ArgfsTer24
NM_001167617.1:c.1107delC NP_001161089.1:p.Ser369ArgfsTer24
NM_001167618.1:c.678delC NP_001161090.1:p.Ser226ArgfsTer24
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
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
Pathogenic 2022-06-21 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.121 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000249.4(MLH1):c.1401del (p.Ser467fs) AND Hereditary cancer-predisposing syndrome 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
rs587781892 dbSNP
Genome
hg38
Position
chr3:37,025,999-37,025,999
Variant Type
snv
Reference Allele
C
Alternative Allele
-
Genome browser