Variant #0000981233 (NC_000015.9:g.45361221del, NM_003104.5:c.757del (SORD))

Chromosome 15
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.45361221del
DNA change (hg38) -
Published as SORD(NM_003104.6):c.757del (p.(Ala253GlnfsTer27)), SORD(NM_003104.6):c.757delG (p.A253Qfs*27)
ISCN -
DB-ID SORD_000002 See all 50 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SORD NM_003104.5 +/. - c.757del r.(?) p.(Ala253GlnfsTer27)


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