Variant #0001040086 (NC_000014.8:g.75475756C>T, NM_001040108.1:c.*8029G>A (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.75475756C>T
DNA change (hg38) -
Published as EIF2B2(NM_014239.4):c.921C>T (p.(Ser307=))
ISCN -
DB-ID EIF2B2_000027
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) 3.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
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.*8029G>A r.(=) p.(=)
EIF2B2 NM_014239.3 ?/. - c.921C>T r.(?) p.(=)


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