Variant #0000001497 (NC_000017.10:g.57161406C>G, NM_015294.3:c.326G>C (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.57161406C>G
DNA change (hg38) g.59084045C>G
Published as -
ISCN -
DB-ID TRIM37_000001
Variant remarks 1 Australian MUL patient (com-het)
Reference PubMed: Hämäläinen et al. 2006
ClinVar ID -
dbSNP ID rs121908391
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 11:18:58 +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 +/+ 5 c.326G>C r.(326g>c) p.(Cys109Ser)


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