Variant #0000283691 (NC_000003.11:g.37090070G>T, NM_000249.3:c.1959G>T (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.37090070G>T
DNA change (hg38) g.37048579G>T
Published as MLH1(NM_000249.2):c.1959G>T, MLH1(NM_000249.3):c.1959G>T (p.L653=, p.(Leu653=)), MLH1(NM_000249.4):c.1959G>T (p.L653=)
ISCN -
DB-ID MLH1_000712 See all 75 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) 0.00834 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 -/. - c.1959G>T r.(?) p.(Leu653=)
LRRFIP2 NM_006309.2 -/. - c.*5272C>A r.(=) p.(=)


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