Variant #0000883144 (NC_000001.10:g.22149897G>A, NM_005529.5:c.13088C>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.22149897G>A
DNA change (hg38) -
Published as HSPG2(NM_005529.5):c.13088C>T (p.(Ser4363Leu)), HSPG2(NM_005529.6):c.13088C>T (p.S4363L)
ISCN -
DB-ID HSPG2_000324 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) 0.00108 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDLRAD2 NM_001013693.2 -?/. - c.*1189G>A r.(=) p.(=)
HSPG2 NM_005529.5 -?/. - c.13088C>T r.(?) p.(Ser4363Leu)


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