Variant #0000617959 (NC_000019.9:g.8649945_8649951dup, NC_000019.9(NM_030957.2):c.3043-12_3043-6dup (ADAMTS10))

Chromosome 19
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.8649945_8649951dup
DNA change (hg38) g.8585061_8585067dup
Published as ADAMTS10(NM_030957.2):c.3043-6_3043-5insGCCCCCT (p.?), ADAMTS10(NM_030957.4):c.3043-6_3043-5insGCCCCCT
ISCN -
DB-ID ADAMTS10_000011 See all 3 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_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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTS10 NM_030957.2 -?/. - c.3043-12_3043-6dup r.(=) p.(=)


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