Variant #0000799119 (NC_000001.10:g.22159838A>G, NM_005529.5:c.11018T>C (HSPG2))

Chromosome 1
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.22159838A>G
DNA change (hg38) -
Published as HSPG2(NM_005529.7):c.11018T>C (p.(Phe3673Ser))
ISCN -
DB-ID HSPG2_000119 See all 2 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) 0.00011 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDLRAD2 NM_001013693.2 ?/. - c.*11130A>G r.(=) p.(=)
HSPG2 NM_005529.5 ?/. - c.11018T>C r.(?) p.(Phe3673Ser)


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