Variant #0000571842 (NC_000022.10:g.33245494G>A, NM_000362.4:c.177G>A (TIMP3))

Chromosome 22
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.33245494G>A
DNA change (hg38) g.32849507G>A
Published as SYN3(NM_001135774.2):c.708+15408C>T, TIMP3(NM_000362.5):c.177G>A (p.T59=)
ISCN -
DB-ID SYN3_000010
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) 0.00014 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     
TIMP3 NM_000362.4 -?/. - c.177G>A r.(?) p.(Thr59=)
SYN3 NM_001135774.1 -?/. - c.708+15408C>T r.(=) p.(=)


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