Variant #0000846970 (NC_000003.11:g.37067306G>A, NM_000249.3:c.1217G>A (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37067306G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MLH1_000481 See all 64 reported entries
Variant remarks Minigene splicing assay (pCAS2.MLH1.ex12): No splicing defect detected; Splicing predictions (MaxEntScan, SpliceSiteFinder-Like, SpliceAI): ΔMES= n.a. ΔSSFL= n.a.
SpliceAI: no splicing defect predicted
Reference PubMed: Tricarico et al 2017
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00088 View details
Owner Alexandra Martins
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2022-04-22 03:42:11 +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 -/. 12 c.1217G>A r.1217g>a p.(Ser406Asn)


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