Variant #0000864144 (NC_000015.9:g.89417659C>G, NM_013227.3:c.7540C>G (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.89417659C>G
DNA change (hg38) -
Published as ACAN(NM_013227.3):c.7540C>G (p.(Gln2514Glu))
ISCN -
DB-ID HAPLN3_000018
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.7540C>G r.(?) p.(Gln2514Glu)
HAPLN3 NM_178232.2 ?/. - c.*3542G>C r.(=) p.(=)


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