Variant #0000001498 (NC_000017.10:g.57157240T>C, NC_000017.10(NM_015294.3):c.493-2A>G (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.57157240T>C
DNA change (hg38) g.59079879T>C
Published as -
ISCN -
DB-ID TRIM37_000002 See all 2 reported entries
Variant remarks Finnish major mutation (FINmajor): 50 Finnish MUL patients (48 hom and 2 com-het)
Reference PubMed: Avela et al. 2000
ClinVar ID -
dbSNP ID rs186251998
Origin SUMMARY record
Segregation yes
Frequency 0/95 FIN CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00082 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-08-29 11:25:34 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_015294.3 +/+ 6i c.493-2A>G r.493_497delgaaag p.Arg166Cysfs*10


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