Variant #0000799118 (NC_000001.10:g.22149967C>T, NM_005529.5:c.13018G>A (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.22149967C>T
DNA change (hg38) -
Published as HSPG2(NM_001291860.1):c.13021G>A (p.(Val4341Met)), HSPG2(NM_005529.6):c.13018G>A (p.V4340M)
ISCN -
DB-ID HSPG2_000291 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) 0.00133 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +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.*1259C>T r.(=) p.(=)
HSPG2 NM_005529.5 -?/. - c.13018G>A r.(?) p.(Val4340Met)


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