Variant #0000883146 (NC_000001.10:g.22155455C>A, NM_005529.5:c.12110G>T (HSPG2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.22155455C>A
DNA change (hg38) -
Published as HSPG2(NM_001291860.1):c.12113G>T (p.R4038L), HSPG2(NM_005529.5):c.12110G>T (p.(Arg4037Leu))
ISCN -
DB-ID HSPG2_000299 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) 0.00092 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 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.*6747C>A r.(=) p.(=)
HSPG2 NM_005529.5 ?/. - c.12110G>T r.(?) p.(Arg4037Leu)


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