Variant #0001046246 (NC_000010.10:g.72643763C>A, NM_003901.3:c.*6671C>A (SGPL1))

Chromosome 10
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.72643763C>A
DNA change (hg38) -
Published as PCBD1(NM_000281.2):c.259G>T (p.(Glu87Ter))
ISCN -
DB-ID PCBD1_000012
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-07-08 13:22:38 +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     
PCBD1 NM_000281.2 +/. - c.259G>T r.(?) p.(Glu87*)
SGPL1 NM_003901.3 +/. - c.*6671C>A r.(=) p.(=)


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