Variant #0000611953 (NC_000009.11:g.136401865_136401880del, NM_001145320.1:c.31_46del (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.136401865_136401880del
DNA change (hg38) g.133536743_133536758del
Published as ADAMTSL2(NM_001145320.1):c.20_35del (p.(Ala11PhefsTer5))
ISCN -
DB-ID ADAMTSL2_000060
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 11:40:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL2 NM_001145320.1 ?/. - c.31_46del r.(?) p.(Ala11PhefsTer5)
ADAMTSL2 NM_014694.3 ?/. - c.31_46del r.(?) p.(Ala11PhefsTer5)


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