Variant #0000864136 (NC_000015.9:g.89416156C>T, NM_013227.3:c.7233C>T (ACAN))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89416156C>T
DNA change (hg38) -
Published as ACAN(NM_001135.3):c.7119C>T (p.(Ala2373=))
ISCN -
DB-ID HAPLN3_000012
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) 0.00082 View details
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 2023-07-07 10:10:56 +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.7233C>T r.(?) p.(Ala2411=)
HAPLN3 NM_178232.2 -?/. - c.*5045G>A r.(=) p.(=)


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