Variant #0000719370 (NC_000003.11:g.37090015dup, NM_000249.3:c.1904dup (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37090015dup
DNA change (hg38) -
Published as MLH1(NM_000249.3):c.1904dupA (p.Asn635Lysfs*10)
ISCN -
DB-ID MLH1_000826 See all 3 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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1904dup r.(?) p.(Asn635Lysfs*10)
LRRFIP2 NM_006309.2 +/. - c.*5328dup r.(?) p.(=)


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