Variant #0000949218 (NC_000009.11:g.136401845G>C, NM_001145320.1:c.11G>C (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.136401845G>C
DNA change (hg38) -
Published as ADAMTSL2(NM_001145320.1):c.11G>C (p.(Arg4Thr))
ISCN -
DB-ID ADAMTSL2_000070
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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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_001145320.1 -?/. - c.11G>C r.(?) p.(Arg4Thr)
ADAMTSL2 NM_014694.3 -?/. - c.11G>C r.(?) p.(Arg4Thr)


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