Variant #0000351145 (NC_000003.11:g.37089130_37089132del, NM_000249.3:c.1852_1854del (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.37089130_37089132del
DNA change (hg38) g.37047639_37047641del
Published as MLH1(NM_000249.3):c.1852_1854del (p.(Lys618del)), MLH1(NM_000249.3):c.1852_1854delAAG (p.K618del), MLH1(NM_000249.4):c.1852_1854delAAG (p.K618del)
ISCN -
DB-ID MLH1_000063 See all 159 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +/. - c.1852_1854del r.(?) p.(Lys618del)
LRRFIP2 NM_006309.2 +/. - c.*6217_*6219del r.(=) p.(=)


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