Variant #0000863671 (NC_000014.8:g.75515668T>G, NM_001040108.1:c.691A>C (MLH3))

Chromosome 14
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.75515668T>G
DNA change (hg38) -
Published as MLH3(NM_001040108.1):c.691A>C (p.(Lys231Gln)), MLH3(NM_001040108.2):c.691A>C (p.K231Q)
ISCN -
DB-ID MLH3_000007 See all 6 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) 0.01229 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
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     
MLH3 NM_001040108.1 -?/. - c.691A>C r.(?) p.(Lys231Gln)
ACYP1 NM_001107.3 -?/. - c.*4479A>C r.(=) p.(=)


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