Variant #0000611955 (NC_000009.11:g.136419687_136419716del, NM_001145320.1:c.1148_1177del (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.136419687_136419716del
DNA change (hg38) g.133554565_133554594del
Published as ADAMTSL2(NM_001145320.1):c.1148_1177delACCGGCTGTTCGGCCACCCGGGCCTGGACA (p.N383_D392del), ADAMTSL2(NM_014694.4):c.1148_1177del (p.(Asn383_Asp392del))...
ISCN -
DB-ID ADAMTSL2_000015 See all 4 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.1148_1177del r.(?) p.(Asn383_Asp392del)
ADAMTSL2 NM_014694.3 -?/. - c.1148_1177del r.(?) p.(Asn383_Asp392del)


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