Variant #0000506912 (NC_000001.10:g.26384973G>A, NM_032588.3:c.739C>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.26384973G>A
DNA change (hg38) g.26058482G>A
Published as TRIM63(NM_032588.3):c.739C>T (p.Q247*, p.(Gln247*)), TRIM63(NM_032588.4):c.739C>T (p.Q247*)
ISCN -
DB-ID TRIM63_000011 See all 11 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) 0.00066 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM63 NM_032588.3 -?/. - c.739C>T r.(?) p.(Gln247Ter)


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