ClinVar Miner

List of variants in gene SPINK5 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
NC_000005.9:g.147480899G>A
NM_006846.3(SPINK5):c.1087T>C (p.Tyr363His) rs1554104431
NM_006846.3(SPINK5):c.1366G>T (p.Asp456Tyr) rs757370601
NM_006846.3(SPINK5):c.1480-10C>A rs375718943
NM_006846.3(SPINK5):c.1960C>T (p.Arg654Cys) rs199567491
NM_006846.3(SPINK5):c.1964G>A (p.Gly655Asp) rs142227576
NM_006846.3(SPINK5):c.2208_2210CAA[1] (p.Asn738del) rs781321238
NM_006846.3(SPINK5):c.2243A>G (p.Glu748Gly) rs181639116
NM_006846.3(SPINK5):c.2441+7A>G rs794727403
NM_006846.3(SPINK5):c.2494_2511ACAGGAGAAAGGAGCAAT[1] (p.832_837TGERSN[1]) rs554634510
NM_006846.3(SPINK5):c.2739+10del rs769519367
NM_006846.3(SPINK5):c.2964G>A (p.Leu988=) rs760791426
NM_006846.3(SPINK5):c.410+6T>C rs1554103297
NM_006846.3(SPINK5):c.411-5T>A rs775468293

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.