Variant #0001060426 (NC_000003.11:g.4461747C>T, NC_000003.11(NM_182760.3):c.602+1G>A (SUMF1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.4461747C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SUMF1_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs143616931
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-12-02 06:10:01 +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     
SUMF1 NM_182760.3 +/. - c.602+1G>A r.(?) p.(?)


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