ClinVar Miner

List of variants in gene DNAI2 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_023036.6(DNAI2):c.1672G>A (p.Ala558Thr) rs1979370 0.77449
NM_023036.6(DNAI2):c.1062A>G (p.Glu354=) rs8073660 0.50668
NM_023036.6(DNAI2):c.1347+7C>T rs2290955 0.46912
NM_023036.6(DNAI2):c.865-5A>G rs8076337 0.32904
NM_023036.6(DNAI2):c.1483G>A (p.Val495Ile) rs28725418 0.17848
NM_023036.6(DNAI2):c.834C>T (p.Thr278=) rs34159194 0.12850
NM_023036.6(DNAI2):c.1053G>A (p.Thr351=) rs34392071 0.04853
NM_023036.6(DNAI2):c.1131G>A (p.Pro377=) rs59499600 0.01236
NM_023036.6(DNAI2):c.590A>T (p.Asp197Val) rs35636875 0.01015
NM_023036.6(DNAI2):c.234G>A (p.Glu78=) rs35985071 0.00904
NM_023036.6(DNAI2):c.1431C>G (p.Thr477=) rs144035254 0.00581
NM_023036.6(DNAI2):c.1462C>T (p.Leu488Phe) rs61736879 0.00529
NM_023036.6(DNAI2):c.865-18C>T rs117075898 0.00470
NM_023036.6(DNAI2):c.747C>T (p.Gly249=) rs148488355 0.00458
NM_023036.6(DNAI2):c.124G>A (p.Val42Met) rs151176313 0.00389
NM_023036.6(DNAI2):c.949G>A (p.Ala317Thr) rs145798624 0.00383
NM_023036.6(DNAI2):c.759G>A (p.Ala253=) rs142656395 0.00370
NM_023036.6(DNAI2):c.468-4G>T rs146462823 0.00321
NM_023036.6(DNAI2):c.1660G>A (p.Asp554Asn) rs117932646 0.00161
NM_023036.6(DNAI2):c.598A>C (p.Ile200Leu) rs144786630 0.00121
NM_023036.6(DNAI2):c.754G>A (p.Val252Met) rs140326154 0.00087
NM_023036.6(DNAI2):c.1715C>T (p.Pro572Leu) rs151241589 0.00081
NM_023036.6(DNAI2):c.1572G>A (p.Lys524=) rs2279122 0.00066
NM_023036.6(DNAI2):c.1629G>A (p.Ala543=) rs201925425 0.00019
NM_023036.6(DNAI2):c.1485A>G (p.Val495=) rs200587166 0.00009
NM_023036.6(DNAI2):c.396G>A (p.Glu132=) rs777369529 0.00006
NM_023036.6(DNAI2):c.933G>A (p.Lys311=) rs570168701 0.00004
NM_023036.6(DNAI2):c.1347+13T>G rs534223470 0.00001
NM_023036.6(DNAI2):c.1530G>A (p.Leu510=) rs747447796 0.00001
NM_023036.6(DNAI2):c.123C>T (p.Phe41=) rs542439989
NM_023036.6(DNAI2):c.1644C>A (p.Ala548=) rs9908476
NM_023036.6(DNAI2):c.1644C>T (p.Ala548=) rs9908476
NM_023036.6(DNAI2):c.685T>G (p.Ser229Ala) rs576683556
NM_023036.6(DNAI2):c.724+24del rs771046755
NM_023036.6(DNAI2):c.724+24dup
NM_023036.6(DNAI2):c.987+17G>T

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.