Variant #0001078404 (NC_000017.10:g.38798707C>T, NM_003079.4:c.156G>A (SMARCE1))

Chromosome 17
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.38798707C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SMARCE1_000044
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1240295309
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-04 18:01:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCE1 NM_003079.4 ?/. - c.156G>A r.(?) p.(Thr52=)


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