Variant #0000282200 (NC_000001.10:g.22150160G>T, NM_005529.5:c.12952C>A (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.22150160G>T
DNA change (hg38) g.21823667G>T
Published as HSPG2(NM_005529.7):c.12952C>A (p.R4318=), LDLRAD2(NM_001013693.3):c.*1452G>T
ISCN -
DB-ID HSPG2_000013
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) 0.17949 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDLRAD2 NM_001013693.2 -/. - c.*1452G>T r.(=) p.(=)
HSPG2 NM_005529.5 -/. - c.12952C>A r.(?) p.(Arg4318=)


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