Variant #0000314824 (NC_000002.11:g.27505680C>T, NM_187841.2:c.81C>T (TRIM54))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27505680C>T
DNA change (hg38) g.27282812C>T
Published as TRIM54(NM_032546.4):c.81C>T (p.P27=)
ISCN -
DB-ID TRIM54_000001
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) 0.00132 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UCN NM_003353.2 -/. - c.*24709G>A r.(=) p.(=)
SLC30A3 NM_003459.4 -/. - c.-19906G>A r.(?) p.(=)
DNAJC5G NM_173650.1 -/. - c.*2402C>T r.(=) p.(=)
TRIM54 NM_187841.2 -/. - c.81C>T r.(?) p.(Pro27=)


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