Variant #0001013871 (NC_000003.11:g.37092068_37092069del, NM_000249.3:c.2195_2196del (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.37092068_37092069del
DNA change (hg38) -
Published as MLH1(NM_000249.3):c.2195_2196del (p.(Lys732ThrfsTer13)), MLH1(NM_000249.3):c.2195_2196delAA (p.K732Tfs*13)
ISCN -
DB-ID MLH1_001680 See all 2 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 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +/. - c.2195_2196del r.(?) p.(Lys732ThrfsTer13)
LRRFIP2 NM_006309.2 +/. - c.*3274_*3275del r.(=) p.(=)


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