Variant #0000911903 (NC_000003.11:g.37061893T>C, NM_000249.3:c.977T>C (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37061893T>C
DNA change (hg38) -
Published as MLH1(NM_000249.3):c.977T>C (p.(Val326Ala), p.V326A), MLH1(NM_000249.4):c.977T>C (p.V326A), MLH1(NM_001258274.3):c.254T>C (p.V85A)
ISCN -
DB-ID MLH1_000433 See all 59 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) 0.00048 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +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.977T>C r.(?) p.(Val326Ala)


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