Unique variants in gene UCHL3

Information The variants shown are described using the NM_006002.4 transcript reference sequence.

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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. 1 - c.482G>A likely benign r.(?) p.(Ser161Asn) g.76169058G>A - UCHL3(NM_001270952.1):c.374G>A (p.S125N) - UCHL3_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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