List of variants in gene ATR reported by University of Washington Department of Laboratory Medicine, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.59+1024G>A	rs6788362	0.01367
NM_001184.4(ATR):c.3581+486T>C	rs72996190	0.01246
NM_001184.4(ATR):c.292+745A>C	rs78050501	0.01036
NM_001184.4(ATR):c.59+3019A>C	rs75518582	0.01035
NM_001184.4(ATR):c.7761+375C>T	rs11717703	0.00978
NM_001184.4(ATR):c.3945+483G>A	rs149815404	0.00659
NM_001184.4(ATR):c.7762-209G>T	rs577916091	0.00270
NM_001184.4(ATR):c.7762-208T>C	rs552872123	0.00269
NM_001184.4(ATR):c.6898-69G>A	rs115906468	0.00198
NM_001184.4(ATR):c.7192+98A>G	rs78659656	0.00114
NM_001184.4(ATR):c.3819+389T>C	rs559805028	0.00090
NM_001184.4(ATR):c.6687+210T>G	rs869312485	0.00012
NM_001184.4(ATR):c.3172-266C>A	rs143205618	0.00010
NM_001184.4(ATR):c.6553-490C>G	rs749552840	0.00009
NM_001184.4(ATR):c.3451-641C>A	rs373891058	0.00008
NM_001184.4(ATR):c.7762-724C>T	rs869312486	0.00004
NM_001184.4(ATR):c.3946-104A>G	rs869312483	0.00003
NM_001184.4(ATR):c.7220G>A (p.Arg2407His)	rs778835776	0.00002
NM_001184.4(ATR):c.2079-28T>C	rs767195127	0.00001
NM_001184.4(ATR):c.4957C>T (p.Arg1653Ter)	rs778813551	0.00001
NM_001184.4(ATR):c.6221+2962T>C	rs869312488	0.00001
NM_001184.4(ATR):c.2533-17T>C	rs869312489
NM_001184.4(ATR):c.3358-1899T>G	rs869312482
NM_001184.4(ATR):c.3450+567A>G	rs564240158
NM_001184.4(ATR):c.3726-24C>A	rs869312487
NM_001184.4(ATR):c.3952del (p.Lys1317_Leu1318insTer)	rs869312789
NM_001184.4(ATR):c.5380+341A>T	rs869312490
NM_001184.4(ATR):c.7762-439T>C	rs869312484

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