List of variants in gene DNAI2 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_023036.6(DNAI2):c.725-27C>T	rs72848284	0.02780
NM_023036.6(DNAI2):c.197G>T (p.Arg66Leu)	rs147470752	0.00092
NM_023036.6(DNAI2):c.1715C>T (p.Pro572Leu)	rs151241589	0.00081
NM_023036.6(DNAI2):c.1380G>T (p.Val460=)	rs148947094	0.00043
NM_023036.6(DNAI2):c.1179A>G (p.Glu393=)	rs146478497	0.00019
NM_023036.6(DNAI2):c.*18C>T	rs369270232	0.00011
NM_023036.6(DNAI2):c.1485A>G (p.Val495=)	rs200587166	0.00009
NM_023036.6(DNAI2):c.855G>A (p.Thr285=)	rs144909415	0.00008
NM_023036.6(DNAI2):c.1251C>T (p.Pro417=)	rs139319121	0.00007
NM_023036.6(DNAI2):c.*22G>A	rs139420980	0.00004
NM_023036.6(DNAI2):c.1011C>T (p.Thr337=)	rs768490008	0.00004
NM_023036.6(DNAI2):c.1446G>T (p.Ser482=)	rs368217836	0.00004
NM_023036.6(DNAI2):c.933G>A (p.Lys311=)	rs570168701	0.00004
NM_023036.6(DNAI2):c.657C>T (p.Leu219=)	rs539461253	0.00003
NM_023036.6(DNAI2):c.43G>A (p.Gly15Arg)	rs758997612	0.00001
NM_023036.6(DNAI2):c.45G>A (p.Gly15=)	rs751121542	0.00001
NM_023036.6(DNAI2):c.467+10T>C	rs377310209	0.00001
NM_023036.6(DNAI2):c.-7C>T
NM_023036.6(DNAI2):c.123C>T (p.Phe41=)	rs542439989
NM_023036.6(DNAI2):c.1348-16C>T
NM_023036.6(DNAI2):c.1348-39CT[2]	rs35732837
NM_023036.6(DNAI2):c.1644C>T (p.Ala548=)	rs9908476
NM_023036.6(DNAI2):c.258C>T (p.Asn86=)	rs886038678
NM_023036.6(DNAI2):c.648G>A (p.Ser216=)
NM_023036.6(DNAI2):c.981T>C (p.Ser327=)	rs886038679

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