ClinVar Miner

List of variants in gene CPLANE1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP
NM_023073.3(CPLANE1):c.1173T>G (p.Ala391=) rs61733482
NM_023073.3(CPLANE1):c.1467C>A (p.Val489=) rs1294855346
NM_023073.3(CPLANE1):c.147G>A (p.Lys49=) rs1554117690
NM_023073.3(CPLANE1):c.1602G>A (p.Val534=) rs751572533
NM_023073.3(CPLANE1):c.1736C>T (p.Ala579Val) rs191239995
NM_023073.3(CPLANE1):c.1839A>G (p.Lys613=) rs533310477
NM_023073.3(CPLANE1):c.1883G>A (p.Arg628Lys) rs74975451
NM_023073.3(CPLANE1):c.2132C>T (p.Ser711Leu) rs116237993
NM_023073.3(CPLANE1):c.2613C>G (p.Arg871=) rs1057521941
NM_023073.3(CPLANE1):c.3537T>C (p.Ala1179=) rs774018842
NM_023073.3(CPLANE1):c.4460G>A (p.Ser1487Asn) rs138157520
NM_023073.3(CPLANE1):c.4481+14C>A rs903055165
NM_023073.3(CPLANE1):c.4698A>G (p.Leu1566=) rs143312971
NM_023073.3(CPLANE1):c.4793C>A (p.Thr1598Lys) rs147588579
NM_023073.3(CPLANE1):c.4947A>G (p.Ser1649=) rs554711652
NM_023073.3(CPLANE1):c.4954C>T (p.Leu1652=) rs141109938
NM_023073.3(CPLANE1):c.5928G>A (p.Gly1976=) rs34161326
NM_023073.3(CPLANE1):c.6328A>G (p.Asn2110Asp) rs139528477
NM_023073.3(CPLANE1):c.662T>C (p.Val221Ala) rs370118778
NM_023073.3(CPLANE1):c.6905C>T (p.Thr2302Met) rs34737149
NM_023073.3(CPLANE1):c.7080G>A (p.Pro2360=) rs769298457
NM_023073.3(CPLANE1):c.7234-7C>G rs141575785
NM_023073.3(CPLANE1):c.7428G>T (p.Leu2476=) rs145750519
NM_023073.3(CPLANE1):c.7866C>T (p.Ser2622=) rs141486731
NM_023073.3(CPLANE1):c.7958-6A>G rs373606578
NM_023073.3(CPLANE1):c.8013A>C (p.Ala2671=) rs201122718
NM_023073.3(CPLANE1):c.8130G>A (p.Gln2710=) rs766837329
NM_023073.3(CPLANE1):c.8182C>A (p.Pro2728Thr) rs77014998
NM_023073.3(CPLANE1):c.82-16A>G rs1169604326
NM_023073.3(CPLANE1):c.8439C>G (p.Ser2813=) rs754005437
NM_023073.3(CPLANE1):c.8796+4A>C rs199810663
NM_023073.3(CPLANE1):c.9252G>A (p.Pro3084=) rs377707922
NM_023073.3(CPLANE1):c.938+19_938+22delGTCT rs748583943
NM_023073.3(CPLANE1):c.994A>G (p.Met332Val) rs369404481

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.