Variant #0001075680 (NC_000009.11:g.140513464C>T, NM_024757.4:c.-17C>T (EHMT1))

Chromosome 9
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.140513464C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID EHMT1_000259
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs946293233
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-29 09:33:02 +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     
EHMT1 NM_024757.4 -?/. - c.-17C>T r.(?) p.(?)


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