Variant #0000571845 (NC_000022.10:g.33255314C>T, NM_000362.4:c.586C>T (TIMP3))

Chromosome 22
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.33255314C>T
DNA change (hg38) g.32859327C>T
Published as TIMP3(NM_000362.4):c.586C>T (p.R196*)
ISCN -
DB-ID SYN3_000013
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 12:08:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TIMP3 NM_000362.4 ?/. - c.586C>T r.(?) p.(Arg196Ter)
SYN3 NM_001135774.1 ?/. - c.708+5588G>A r.(=) p.(=)


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