Variant #0000001499 (NC_000017.10:g.57148248G>A, NM_015294.3:c.745C>T (TRIM37))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57148248G>A
DNA change (hg38) g.59070887G>A
Published as -
ISCN -
DB-ID TRIM37_000003
Variant remarks 1 Canadian MUL patient (com-het)
Reference PubMed: Hämäläinen et al. 2004
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/85 CEPH
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-08-29 11:37:24 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_015294.3 +/+ 9 c.745C>T r.(745c>u) p.(Gln249*)


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