Variant #0000923921 (NC_000003.11:g.37089022C>T, NM_000249.3:c.1744C>T (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37089022C>T
DNA change (hg38) -
Published as MLH1(NM_000249.3):c.1744C>T (p.L582F, p.(Leu582Phe), p.Leu582Phe), MLH1(NM_000249.4):c.1744C>T (p.L582F)
ISCN -
DB-ID MLH1_000635 See all 20 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +?/. - c.1744C>T r.(?) p.(Leu582Phe)


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