Variant #0000016107 (NC_000017.10:g.57134269T>C, NM_015294.3:c.1166A>G (TRIM37))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57134269T>C
DNA change (hg38) g.59056908T>C
Published as -
ISCN -
DB-ID TRIM37_000018
Variant remarks 1 Finnish MUL patient (com-het)
Reference Hämäläinen, Lipsanen-Nyman, Lehesjoki, unpublished data
ClinVar ID -
dbSNP ID rs312262705
Origin SUMMARY record
Segregation yes
Frequency 0/95 CEPH
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 2012-09-25 14:35:54 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 +?/+? 13 c.1166A>G r.(1166a>g) p.(Tyr389Cys)
TRIM37 NM_015294.3 +?/+? 13 c.1166A>G r.(1166a>g) p.(Tyr389Cys)


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