Variant #0000355590 (NC_000003.11:g.37030175C>A, MLH1(NM_000249.3):c.-4864C>A)

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method InSiGHT
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37030175C>A
DNA change (hg38) g.36988684C>A
Published as -
ISCN -
DB-ID MLH1_000938 See all 3 reported entries
Variant remarks Insight class: 1
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner InSiGHT - John-Paul Plazzer
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 -/- _1 c.-4864C>A r.(=) p.(=)