Variant #0000887457 (NC_000006.11:g.7585514C>T, NM_004415.2:c.8019C>T (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.7585514C>T
DNA change (hg38) -
Published as DSP(NM_004415.2):c.8019C>T (p.D2673=)
ISCN -
DB-ID DSP_000268 See all 3 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) 0.0002 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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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.8019C>T r.(?) p.(Asp2673=) -
SNRNP48 NM_152551.3 -?/. - c.-4977C>T r.(?) p.(=) -


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