Variant #0000717205 (NC_000001.10:g.22214536T>A, NM_005529.5:c.598A>T (HSPG2))

Chromosome 1
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.22214536T>A
DNA change (hg38) -
Published as HSPG2(NM_005529.5):c.598A>T (p.(Thr200Ser))
ISCN -
DB-ID HSPG2_000288
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) 0.0001 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDLRAD2 NM_001013693.2 -?/. - c.*65828T>A r.(=) p.(=)
HSPG2 NM_005529.5 -?/. - c.598A>T r.(?) p.(Thr200Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.