Variant #0000981487 (NC_000015.9:g.89417117G>A, NM_013227.3:c.7378G>A (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.89417117G>A
DNA change (hg38) -
Published as ACAN(NM_013227.3):c.7378G>A (p.(Gly2460Arg)), ACAN(NM_013227.4):c.7378G>A (p.G2460R)
ISCN -
DB-ID HAPLN3_000017 See all 3 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) 0.00014 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAN NM_013227.3 ?/. - c.7378G>A r.(?) p.(Gly2460Arg)
HAPLN3 NM_178232.2 ?/. - c.*4084C>T r.(=) p.(=)


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