Gene dossier

IDS

50 mutation records across 1 cancer labels and 1 source families.

0 actionable0 hotspotsNot reported
Top records

Prioritized variant evidence

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VariantCancerEvidenceFrequencySources
IDS p.Gly374=
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gly374=
substitution
UNSPECDriverNot reportedClinVar
IDS p.Glu274Ter
substitution
UNSPECDriverNot reportedClinVar
IDS p.Glu274Ter
substitution
UNSPECDriverNot reportedClinVar
IDS c.708+1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.708+1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gly312Ser
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gly312Ser
substitution
UNSPECDriverNot reportedClinVar
IDS p.Thr367Ser
substitution
UNSPECDriverNot reportedClinVar
IDS p.Thr367Ser
substitution
UNSPECDriverNot reportedClinVar
IDS c.419-1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.419-1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS p.Lys236=
substitution
UNSPECDriverNot reportedClinVar
IDS p.Lys236=
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gln204Ter
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gln204Ter
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gly224Arg
substitution
UNSPECDriverNot reportedClinVar
IDS p.Gly224Arg
substitution
UNSPECDriverNot reportedClinVar
IDS c.1006+1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.1006+1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.709-1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.709-1G>A
substitution
UNSPECDriverNot reportedClinVar
IDS c.104-2A>C
substitution
UNSPECDriverNot reportedClinVar
IDS c.104-2A>C
substitution
UNSPECDriverNot reportedClinVar
IDS p.Trp267Cys
substitution
UNSPECDriverNot reportedClinVar
IDS p.Trp267Cys
substitution
UNSPECDriverNot reportedClinVar
IDS c.104-2A>G
substitution
UNSPECDriverNot reportedClinVar
IDS c.104-2A>G
substitution
UNSPECDriverNot reportedClinVar
IDS c.708+2T>C
substitution
UNSPECDriverNot reportedClinVar
IDS c.708+2T>C
substitution
UNSPECDriverNot reportedClinVar