Variant #0000505601 (NC_000001.10:g.22200454G>T, NM_005529.5:c.3707C>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.22200454G>T
DNA change (hg38) g.21873961G>T
Published as HSPG2(NM_001291860.1):c.3710C>A (p.A1237E, p.(Ala1237Glu)), HSPG2(NM_001291860.2):c.3710C>A (p.A1237E)
ISCN -
DB-ID HSPG2_000006 See all 4 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) 0.00166 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*51746G>T r.(=) p.(=)
HSPG2 NM_005529.5 -?/. - c.3707C>A r.(?) p.(Ala1236Glu)


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