Variant #0000285143 (NC_000001.10:g.22155353G>A, NM_005529.5:c.12212C>T (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.22155353G>A
DNA change (hg38) g.21828860G>A
Published as HSPG2(NM_005529.6):c.12212C>T (p.A4071V)
ISCN -
DB-ID HSPG2_000020 See all 3 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) 0.02906 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*6645G>A r.(=) p.(=)
HSPG2 NM_005529.5 -/. - c.12212C>T r.(?) p.(Ala4071Val)


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