Variant #0001031677 (NC_000001.10:g.22154387G>A, NM_005529.5:c.12558C>T (HSPG2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.22154387G>A
DNA change (hg38) -
Published as HSPG2(NM_005529.7):c.12558C>T (p.(Ser4186=))
ISCN -
DB-ID HSPG2_000390
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) 0.04077 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 2025-05-05 21:14:00 +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     
LDLRAD2 NM_001013693.2 -/. - c.*5679G>A r.(=) p.(=)
HSPG2 NM_005529.5 -/. - c.12558C>T r.(?) p.(=)


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