Variant #0000536980 (NC_000009.11:g.136403503C>A, NM_001145320.1:c.266C>A (ADAMTSL2))

Chromosome 9
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.136403503C>A
DNA change (hg38) g.133538381C>A
Published as ADAMTSL2(NM_001145320.2):c.266C>A (p.T89N)
ISCN -
DB-ID ADAMTSL2_000028
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL2 NM_001145320.1 ?/. - c.266C>A r.(?) p.(Thr89Asn)
ADAMTSL2 NM_014694.3 ?/. - c.266C>A r.(?) p.(Thr89Asn)


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