ClinVar Miner

List of variants in gene SPINK5 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP
NM_006846.3(SPINK5):c.*208C>G rs3088193
NM_006846.3(SPINK5):c.*330T>C rs72660265
NM_006846.3(SPINK5):c.*361_*363dup rs397704765
NM_006846.3(SPINK5):c.*44T>C rs4349706
NM_006846.3(SPINK5):c.1004C>T (p.Ala335Val) rs34482796
NM_006846.3(SPINK5):c.1011-12C>T rs1422991
NM_006846.3(SPINK5):c.1093-10A>G rs2303062
NM_006846.3(SPINK5):c.1103G>A (p.Ser368Asn) rs2303063
NM_006846.3(SPINK5):c.1156G>A (p.Asp386Asn) rs2303064
NM_006846.3(SPINK5):c.1188T>C (p.His396=) rs2303065
NM_006846.3(SPINK5):c.1258A>G (p.Lys420Glu) rs2303067
NM_006846.3(SPINK5):c.1389A>G (p.Gly463=) rs6896303
NM_006846.3(SPINK5):c.1557C>A (p.Gly519=) rs880687
NM_006846.3(SPINK5):c.1659C>T (p.Val553=) rs2303071
NM_006846.3(SPINK5):c.2132G>A (p.Arg711Gln) rs3777134
NM_006846.3(SPINK5):c.2358C>T (p.Leu786=) rs17704908
NM_006846.3(SPINK5):c.2412C>T (p.Gly804=) rs33920397
NM_006846.3(SPINK5):c.2475G>T (p.Glu825Asp) rs2303070
NM_006846.3(SPINK5):c.2667-13A>T rs2052537
NM_006846.3(SPINK5):c.3009T>C (p.Gly1003=) rs2400478
NM_006846.3(SPINK5):c.800A>G (p.Gln267Arg) rs6892205

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.