ClinVar Miner

List of variants in gene AIP reported as benign for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_003977.4(AIP):c.*60G>C rs146014363
NM_003977.4(AIP):c.*64G>A rs115346238
NM_003977.4(AIP):c.-23A>G rs200665479
NM_003977.4(AIP):c.-84C>G rs540839310
NM_003977.4(AIP):c.132C>T (p.Asp44=) rs11822907
NM_003977.4(AIP):c.144C>T (p.Thr48=) rs772658134
NM_003977.4(AIP):c.301G>A (p.Val101Met) rs147931650
NM_003977.4(AIP):c.366C>T (p.Cys122=) rs748883061
NM_003977.4(AIP):c.36G>A (p.Gly12=) rs79662690
NM_003977.4(AIP):c.516C>T (p.Asp172=) rs2276020
NM_003977.4(AIP):c.517G>A (p.Glu173Lys) rs138902236
NM_003977.4(AIP):c.571C>T (p.Arg191Cys) rs189861025
NM_003977.4(AIP):c.682C>A (p.Gln228Lys) rs641081
NM_003977.4(AIP):c.68G>A (p.Gly23Glu) rs116940576
NM_003977.4(AIP):c.753G>A (p.Leu251=) rs147351993
NM_003977.4(AIP):c.891C>A (p.Ala297=) rs35665586
NM_003977.4(AIP):c.920= (p.Arg307=) rs4930199

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.