Variant #0000725354 (NC_000015.9:g.89417692C>T, NM_013227.3:c.7573C>T (ACAN))

Chromosome 15
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.89417692C>T
DNA change (hg38) -
Published as ACAN(NM_001135.3):c.7276C>T (p.(Arg2426Cys))
ISCN -
DB-ID HAPLN3_000011 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAN NM_013227.3 ?/. - c.7573C>T r.(?) p.(Arg2525Cys)
HAPLN3 NM_178232.2 ?/. - c.*3509G>A r.(=) p.(=)


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