ClinVar Miner

List of variants in gene AKAP9 reported by Blueprint Genetics,

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_005751.4(AKAP9):c.10022C>T (p.Ser3341Leu) rs587782932
NM_005751.4(AKAP9):c.10163G>C (p.Arg3388Thr) rs765397069
NM_005751.4(AKAP9):c.1067A>T (p.Asp356Val) rs533277424
NM_005751.4(AKAP9):c.1099G>A (p.Val367Met) rs138161478
NM_005751.4(AKAP9):c.11276C>T (p.Pro3759Leu) rs869025356
NM_005751.4(AKAP9):c.11378C>G (p.Ser3793Cys) rs730880044
NM_005751.4(AKAP9):c.11498C>G (p.Ser3833Ter) rs869025357
NM_005751.4(AKAP9):c.1489G>T (p.Glu497Ter) rs730880043
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
NM_005751.4(AKAP9):c.3953-3T>C rs730880045
NM_005751.4(AKAP9):c.4825_4826delinsCA (p.Arg1609Gln) rs786205707
NM_005751.4(AKAP9):c.5272G>C (p.Asp1758His) rs142603711
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.7314A>T (p.Glu2438Asp) rs138468216
NM_005751.4(AKAP9):c.73G>A (p.Ala25Thr) rs730880042
NM_005751.4(AKAP9):c.8345C>T (p.Thr2782Ile) rs543634397
NM_005751.4(AKAP9):c.8656A>G (p.Ile2886Val) rs143283097
NM_005751.4(AKAP9):c.9112C>T (p.Arg3038Cys) rs753467156
NM_005751.4(AKAP9):c.9338dup (p.Ser3114fs) rs869025358

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.