Variant #0001078444 (NC_000008.10:g.77593762T>C, NM_024721.4:c.-140T>C (ZFHX4))

Chromosome 8
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.77593762T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ZFHX4_000074
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs144397783
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 2026-06-09 09:45:01 +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     
ZFHX4 NM_024721.4 -?/. - c.-140T>C r.(?) p.(?)


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