Variant #0001080052 (NC_000006.11:g.116948999del, NM_001010892.2:c.1129del (RSPH4A))

Chromosome 6
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.116948999del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr6_008323
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2482802957
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 2026-07-13 10:13:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RSPH4A NM_001010892.2 +/. - c.1129del r.(?) p.(Glu377LysfsTer11)


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