ClinVar Miner

List of variants reported as uncertain significance for Cayman type cerebellar ataxia by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP
NM_033064.4(ATCAY):c.*1167G>A rs751398427
NM_033064.4(ATCAY):c.*1180C>T rs140608538
NM_033064.4(ATCAY):c.*1181G>A rs530991790
NM_033064.4(ATCAY):c.*1188G>T rs886054420
NM_033064.4(ATCAY):c.*1193T>A rs192536222
NM_033064.4(ATCAY):c.*1409T>C rs886054421
NM_033064.4(ATCAY):c.*1427A>T rs536842684
NM_033064.4(ATCAY):c.*143G>A rs537298270
NM_033064.4(ATCAY):c.*1535G>A rs886054422
NM_033064.4(ATCAY):c.*1632T>C rs546859649
NM_033064.4(ATCAY):c.*1761C>T rs777283516
NM_033064.4(ATCAY):c.*192_*193delTT rs796133913
NM_033064.4(ATCAY):c.*2026G>A rs147402942
NM_033064.4(ATCAY):c.*2265G>A rs886054423
NM_033064.4(ATCAY):c.*2297C>A rs886054424
NM_033064.4(ATCAY):c.*2311G>A rs186330129
NM_033064.4(ATCAY):c.*2356C>T rs886054425
NM_033064.4(ATCAY):c.*2426C>T rs886054426
NM_033064.4(ATCAY):c.*2668G>A rs555029183
NM_033064.4(ATCAY):c.*266C>T rs867087852
NM_033064.4(ATCAY):c.*2742C>T rs769121113
NM_033064.4(ATCAY):c.*2996G>A rs886054427
NM_033064.4(ATCAY):c.*3108C>T rs143949702
NM_033064.4(ATCAY):c.*313G>A rs141455019
NM_033064.4(ATCAY):c.*3203G>A rs539627639
NM_033064.4(ATCAY):c.*3376C>T rs76339349
NM_033064.4(ATCAY):c.*391C>A rs765579267
NM_033064.4(ATCAY):c.*441G>A rs117035326
NM_033064.4(ATCAY):c.*441G>C rs117035326
NM_033064.4(ATCAY):c.*496C>A rs886054417
NM_033064.4(ATCAY):c.*681A>G rs772852314
NM_033064.4(ATCAY):c.*687C>A rs377406299
NM_033064.4(ATCAY):c.*728T>C rs371256803
NM_033064.4(ATCAY):c.*740G>A rs569661909
NM_033064.4(ATCAY):c.*813G>C rs886054418
NM_033064.4(ATCAY):c.*939G>A rs886054419
NM_033064.4(ATCAY):c.-198C>G rs553381633
NM_033064.4(ATCAY):c.-375G>T rs886054373
NM_033064.4(ATCAY):c.-390A>G rs140876148
NM_033064.4(ATCAY):c.-398C>A rs186140929
NM_033064.4(ATCAY):c.162C>T (p.Asn54=) rs373392142
NM_033064.4(ATCAY):c.36C>T (p.Asn12=) rs368213837
NM_033064.4(ATCAY):c.405G>A (p.Ala135=) rs202077180
NM_033064.4(ATCAY):c.478G>A (p.Gly160Arg) rs374611192
NM_033064.4(ATCAY):c.544+16dupC rs140914543
NM_033064.4(ATCAY):c.544+6dupA rs749475336
NM_033064.4(ATCAY):c.555C>A (p.Gly185=) rs367736161
NM_033064.4(ATCAY):c.568G>A (p.Ala190Thr) rs537155754
NM_033064.4(ATCAY):c.647+10C>T rs181866005
NM_033064.4(ATCAY):c.678G>A (p.Val226=) rs886054415
NM_033064.4(ATCAY):c.717G>A (p.Thr239=) rs768556456

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.