Variant #0000529787 (NC_000006.11:g.7585887A>T, NM_004415.2:c.8392A>T (DSP))

Chromosome 6
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.7585887A>T
DNA change (hg38) g.7585654A>T
Published as DSP(NM_004415.4):c.8392A>T (p.T2798S)
ISCN -
DB-ID DSP_000698 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DSP NM_004415.2 ?/. - c.8392A>T r.(?) p.(Thr2798Ser) -
SNRNP48 NM_152551.3 ?/. - c.-4604A>T r.(?) p.(=) -


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