Variant #0000923161 (NC_000001.10:g.26393843G>A, NM_032588.3:c.143C>T (TRIM63))

Chromosome 1
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.26393843G>A
DNA change (hg38) -
Published as TRIM63(NM_032588.3):c.143C>T (p.A48V), TRIM63(NM_032588.4):c.143C>T (p.A48V)
ISCN -
DB-ID TRIM63_000008 See all 7 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) 0.00136 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM63 NM_032588.3 -?/. - c.143C>T r.(?) p.(Ala48Val)


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