Variant #0001015266 (NC_000015.9:g.89417237C>T, NM_013227.3:c.7498C>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.89417237C>T
DNA change (hg38) -
Published as ACAN(NM_013227.3):c.7498C>T (p.(Gln2500Ter))
ISCN -
DB-ID HAPLN3_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAN NM_013227.3 ?/. - c.7498C>T r.(?) p.(Gln2500*)
HAPLN3 NM_178232.2 ?/. - c.*3964G>A r.(=) p.(=)


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