Variant #0000806496 (NC_000014.8:g.75516289G>C, NM_001040108.1:c.70C>G (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.75516289G>C
DNA change (hg38) -
Published as MLH3(NM_001040108.1):c.70C>G (p.Q24E)
ISCN -
DB-ID MLH3_000051 See all 14 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.70C>G r.(?) p.(Gln24Glu)
ACYP1 NM_001107.3 ?/. - c.*3858C>G r.(=) p.(=)


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