ClinVar Miner

List of variants in gene WASHC5 reported as likely benign for Spastic paraplegia, autosomal dominant

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_014846.4(WASHC5):c.*269_*270del rs199912701
NM_014846.4(WASHC5):c.*40del rs550928439
NM_014846.4(WASHC5):c.*78A>G rs188863489
NM_014846.4(WASHC5):c.-178T>C rs370705310
NM_014846.4(WASHC5):c.-241G>A rs563795659
NM_014846.4(WASHC5):c.-245C>G rs185375174
NM_014846.4(WASHC5):c.-253G>A rs533362974
NM_014846.4(WASHC5):c.1029A>G (p.Gln343=) rs140523354
NM_014846.4(WASHC5):c.1151-8G>A rs16900335
NM_014846.4(WASHC5):c.1187A>G (p.Lys396Arg) rs142423043
NM_014846.4(WASHC5):c.1245A>G (p.Leu415=) rs10429323
NM_014846.4(WASHC5):c.1408+7A>G rs16900312
NM_014846.4(WASHC5):c.2017-13T>C rs74458977
NM_014846.4(WASHC5):c.2098-13G>A rs375720047
NM_014846.4(WASHC5):c.2100G>A (p.Val700=) rs148936723
NM_014846.4(WASHC5):c.2199+4C>A rs145721086
NM_014846.4(WASHC5):c.2771-7T>C rs142685897
NM_014846.4(WASHC5):c.316A>G (p.Ile106Val) rs142907217
NM_014846.4(WASHC5):c.3225A>G (p.Pro1075=) rs34569226
NM_014846.4(WASHC5):c.3319G>A (p.Val1107Met) rs138407503
NM_014846.4(WASHC5):c.555T>C (p.Asp185=) rs145934920
NM_014846.4(WASHC5):c.636C>T (p.Phe212=) rs190007736
NM_014846.4(WASHC5):c.655G>A (p.Glu219Lys) rs143719918
NM_014846.4(WASHC5):c.732G>A (p.Pro244=) rs146320386

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.