Variant #0001049021 (NC_000003.11:g.37042515A>G, NM_000249.3:c.277A>G (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37042515A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID MLH1_000967 See all 43 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs41295282
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-10 16:02:04 +02:00 (CEST)
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.277A>G r.(?) p.(Ser93Gly)


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