Variant #0000271003 (NC_000006.11:g.7585489C>T, NM_004415.2:c.7994C>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.7585489C>T
DNA change (hg38) g.7585256C>T
Published as DSP(NM_004415.2):c.7994C>T (p.(Thr2665Met), p.T2665M), DSP(NM_004415.4):c.7994C>T (p.T2665M)
ISCN -
DB-ID DSP_000538 See all 5 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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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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.7994C>T r.(?) p.(Thr2665Met) -
SNRNP48 NM_152551.3 ?/. - c.-5002C>T r.(?) p.(=) -


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