Genomic variant #0000000002

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Variant Name delG1702
Clinical Significance Pathogenic
Variant Frequency Multiple cases
Evidences External source reports variant as pathogenic or likely pathogenic
dbSNP ID rs727503967
Reference Scott et al. (1993)
DNA change (genomic) (Relative to hg19 / GRCh37) g.997222delG
Average frequency (large NGS studies) Retrieve
Owner Tamara Simakova




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Protein     

DNA change (cDNA)     
IDUA NM_000203.3 +/+ p.(His539Thrfs*21) c.1614delG