Variant #0000559208 (NC_000016.9:g.77468558G>C, NM_199355.2:c.35C>G (ADAMTS18))

Chromosome 16
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.77468558G>C
DNA change (hg38) g.77434661G>C
Published as ADAMTS18(NM_199355.3):c.35C>G (p.P12R), ADAMTS18(NM_199355.4):c.35C>G (p.P12R)
ISCN -
DB-ID ADAMTS18_000081 See all 2 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) 0.00635 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
ADAMTS18 NM_199355.2 -?/. - c.35C>G r.(?) p.(Pro12Arg)


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