Variant #0001035923 (NC_000006.11:g.7585976_7585987del, NM_004415.2:c.8481_8492del (DSP))

Chromosome 6
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.7585976_7585987del
DNA change (hg38) -
Published as DSP(NM_004415.2):c.8481_8492delCGGCTCCCGCTC (p.S2843_R2846del)
ISCN -
DB-ID DSP_000828 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DSP NM_004415.2 -?/. - c.8481_8492del r.(?) p.(Ser2843_Arg2846del) -
SNRNP48 NM_152551.3 -?/. - c.-4515_-4504del r.(?) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.