Variant #0000001502 (NC_000017.10:g.57141716C>T, NM_015294.3:c.860G>A (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.57141716C>T
DNA change (hg38) g.59064355C>T
Published as -
ISCN -
DB-ID TRIM37_000006
Variant remarks 1 Australian MUL patient (com-het)
Reference PubMed: Hämäläinen et al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-08-29 12:00:21 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_015294.3 +/+ 10 c.860G>A r.810_860del p.Glu271_Ser287del


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