Variant #0000850240 (NC_000003.11:g.37035090C>T, NM_000249.3:c.52C>T (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.37035090C>T
DNA change (hg38) -
Published as MLH1(NM_000249.3):c.52C>T (p.(Arg18Cys)), MLH1(NM_000249.4):c.52C>T (p.R18C)
ISCN -
DB-ID MLH1_001887 See all 12 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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 ?/. - c.52C>T r.(?) p.(Arg18Cys)
EPM2AIP1 NM_014805.3 ?/. - c.-522G>A r.(?) p.(=)


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