Genomic variant #0000313505

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.57125024_57125025insGAAACT
DNA change (hg38) -
Published as TRIM37:c.1667+18_1667+19insAGTTTC
ISCN -
DB-ID TRIM37_000026
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_VUmc




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
TRIM37 NM_001005207.2 -?/. - c.1667+19_1667+20insAGTTTC likely benign r.(=) p.(=)
TRIM37 NM_015294.3 -?/. - c.1667+19_1667+20insAGTTTC likely benign r.(=) p.(=)