Variant #0001078309 (NC_000023.10:g.153047065T>C, NM_014370.3:c.296T>C (SRPK3))

Chromosome X
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.153047065T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SRPK3_000048
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs782110409
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 2026-05-29 15:00:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRPK3 NM_014370.3 ?/. - c.296T>C r.(?) p.(Ile99Thr)


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