Variant #0001019656 (NC_000009.11:g.136404935G>A, NM_014694.3:c.352G>A (ADAMTSL2))

Chromosome 9
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.136404935G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ADAMTSL2_000069 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs374608028
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-12-23 21:35:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL2 NM_014694.3 -?/. - c.352G>A r.(?) p.(Val118Ile)


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