Variant #0000289231 (NC_000001.10:g.22217095C>T, NM_005529.5:c.337G>A (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.22217095C>T
DNA change (hg38) g.21890602C>T
Published as HSPG2(NM_001291860.1):c.337G>A (p.E113K), HSPG2(NM_005529.5):c.337G>A (p.(Glu113Lys))
ISCN -
DB-ID HSPG2_000091 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) 0.00024 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 14:54:23 +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.*68387C>T r.(=) p.(=)
HSPG2 NM_005529.5 ?/. - c.337G>A r.(?) p.(Glu113Lys)


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