Variant #0000858476 (NC_000002.11:g.27522165G>T, NM_187841.2:c.394G>T (TRIM54))

Chromosome 2
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.27522165G>T
DNA change (hg38) -
Published as TRIM54(NM_032546.3):c.394G>T (p.(Glu132*))
ISCN -
DB-ID TRIM54_000007
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) 0.00017 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UCN NM_003353.2 ?/. - c.*8224C>A r.(=) p.(=)
TRIM54 NM_187841.2 ?/. - c.394G>T r.(?) p.(Glu132*)


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