Variant #0001046949 (NC_000004.11:g.73156565C>T, NC_000004.11(NM_014243.2):c.2931+7G>A (ADAMTS3))

Chromosome 4
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.73156565C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ADAMTS3_000038
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs761319867
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-14 15:20:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTS3 NM_014243.2 ?/. - c.2931+7G>A r.(?) p.(?)


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