ClinVar Miner

List of variants in gene GDAP1 studied for Charcot-Marie-Tooth disease

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_018972.2(GDAP1):c.347T>C rs281865060
NM_018972.4(GDAP1):c.100dup (p.Ser34fs)
NM_018972.4(GDAP1):c.1019dup (p.Arg341fs) rs756461496
NM_018972.4(GDAP1):c.101C>G (p.Ser34Cys)
NM_018972.4(GDAP1):c.1031T>G (p.Leu344Arg)
NM_018972.4(GDAP1):c.116del (p.Lys39fs)
NM_018972.4(GDAP1):c.117G>C (p.Lys39Asn)
NM_018972.4(GDAP1):c.172_173delinsTTA (p.Pro59fs)
NM_018972.4(GDAP1):c.174_176delinsTGTG (p.Pro59fs)
NM_018972.4(GDAP1):c.1A>T (p.Met1Leu)
NM_018972.4(GDAP1):c.233C>T (p.Pro78Leu)
NM_018972.4(GDAP1):c.295C>T (p.Gln99Ter)
NM_018972.4(GDAP1):c.310+3A>G
NM_018972.4(GDAP1):c.311-1G>A
NM_018972.4(GDAP1):c.332C>A (p.Pro111His)
NM_018972.4(GDAP1):c.337_340AAAG[1] (p.Glu114fs)
NM_018972.4(GDAP1):c.347T>G (p.Met116Arg) rs281865060
NM_018972.4(GDAP1):c.349dup (p.Tyr117fs)
NM_018972.4(GDAP1):c.358C>G (p.Arg120Gly)
NM_018972.4(GDAP1):c.358C>T (p.Arg120Trp) rs104894078
NM_018972.4(GDAP1):c.359G>A (p.Arg120Gln)
NM_018972.4(GDAP1):c.364C>A (p.Gln122Lys)
NM_018972.4(GDAP1):c.385G>C (p.Asp129His)
NM_018972.4(GDAP1):c.389C>G (p.Ser130Cys)
NM_018972.4(GDAP1):c.433_437del (p.Glu145fs)
NM_018972.4(GDAP1):c.439del (p.Thr147fs)
NM_018972.4(GDAP1):c.445G>T (p.Asp149Tyr)
NM_018972.4(GDAP1):c.458C>T (p.Pro153Leu) rs538412810
NM_018972.4(GDAP1):c.485-2A>G
NM_018972.4(GDAP1):c.501del (p.Glu168fs) rs886041386
NM_018972.4(GDAP1):c.533A>G (p.Asn178Ser)
NM_018972.4(GDAP1):c.558del (p.Ile186fs)
NM_018972.4(GDAP1):c.571C>T (p.Arg191Ter) rs1554547986
NM_018972.4(GDAP1):c.579+1G>A rs864622501
NM_018972.4(GDAP1):c.579del (p.Lys193fs) rs1060500979
NM_018972.4(GDAP1):c.656T>A (p.Val219Asp)
NM_018972.4(GDAP1):c.656T>G (p.Val219Gly)
NM_018972.4(GDAP1):c.664G>A (p.Glu222Lys)
NM_018972.4(GDAP1):c.668T>A (p.Leu223Ter)
NM_018972.4(GDAP1):c.677G>A (p.Arg226Lys)
NM_018972.4(GDAP1):c.678A>C (p.Arg226Ser)
NM_018972.4(GDAP1):c.679A>G (p.Asn227Asp)
NM_018972.4(GDAP1):c.715C>T (p.Leu239Phe) rs104894080
NM_018972.4(GDAP1):c.740C>T (p.Ala247Val)
NM_018972.4(GDAP1):c.767A>G (p.His256Arg) rs1476856429
NM_018972.4(GDAP1):c.769C>T (p.Arg257Ter) rs770501034
NM_018972.4(GDAP1):c.786del (p.Phe263fs) rs1060500978
NM_018972.4(GDAP1):c.811G>A (p.Gly271Arg) rs775622226
NM_018972.4(GDAP1):c.817C>G (p.Arg273Gly)
NM_018972.4(GDAP1):c.836A>G (p.Tyr279Cys)
NM_018972.4(GDAP1):c.840del (p.Tyr279_Tyr280insTer)
NM_018972.4(GDAP1):c.845G>A (p.Arg282His)
NM_018972.4(GDAP1):c.864dup (p.Phe289fs)
NM_018972.4(GDAP1):c.891C>G (p.Asn297Lys)
NM_018972.4(GDAP1):c.928del (p.Arg310fs)
NM_018972.4(GDAP1):c.929G>A (p.Arg310Gln) rs1323153568

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.