Variant #0001026403 (NC_000014.8:g.75516060A>G, NM_001040108.1:c.299T>C (MLH3))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.75516060A>G
DNA change (hg38) -
Published as MLH3(NM_001040108.2):c.299T>C (p.I100T)
ISCN -
DB-ID ACYP1_000014
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 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 2025-02-07 18:57:27 +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     
MLH3 NM_001040108.1 ?/. - c.299T>C r.(?) p.(Ile100Thr)
ACYP1 NM_001107.3 ?/. - c.*4087T>C r.(=) p.(=)


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