List of variants in gene ATR reported as benign for not specified

Minimum submission review status:		Collection method:
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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_001184.4(ATR):c.7875G>A (p.Gln2625=)	rs1802904	0.88595
NM_001184.4(ATR):c.1776T>A (p.Gly592=)	rs2227930	0.63717
NM_001184.4(ATR):c.632T>C (p.Met211Thr)	rs2227928	0.63625
NM_001184.4(ATR):c.1815T>C (p.Asp605=)	rs2227929	0.33689
NM_001184.4(ATR):c.7274G>A (p.Arg2425Gln)	rs2229032	0.12815
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=)	rs2227932	0.07623
NM_001184.4(ATR):c.2442A>G (p.Glu814=)	rs55895932	0.04528
NM_001184.4(ATR):c.1326A>G (p.Lys442=)	rs28897765	0.01766
NM_001184.4(ATR):c.946G>A (p.Val316Ile)	rs28897764	0.01744
NM_001184.4(ATR):c.1950G>A (p.Glu650=)	rs28910270	0.01739
NM_001184.4(ATR):c.2875G>A (p.Val959Met)	rs28910271	0.01643
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser)	rs55894265	0.01275
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala)	rs33972295	0.01261
NM_001184.4(ATR):c.5739-7_5739-6del	rs72371423	0.01173
NM_001184.4(ATR):c.891G>C (p.Lys297Asn)	rs2229033	0.01036
NM_001184.4(ATR):c.4002G>A (p.Gln1334=)	rs56026468	0.01034
NM_001184.4(ATR):c.5868C>T (p.Tyr1956=)	rs112018640	0.01020
NM_001184.4(ATR):c.268C>T (p.His90Tyr)	rs28897763	0.00813
NM_001184.4(ATR):c.1328G>C (p.Arg443Thr)	rs28367453	0.00450
NM_001184.4(ATR):c.423T>C (p.Ile141=)	rs10935466	0.00416
NM_001184.4(ATR):c.4764C>T (p.Leu1588=)	rs142240637	0.00415
NM_001184.4(ATR):c.4576A>G (p.Ile1526Val)	rs34124242	0.00145
NM_001184.4(ATR):c.3120G>A (p.Leu1040=)	rs28910272
NM_001184.4(ATR):c.4153-21dup	rs112116713
NM_001184.4(ATR):c.5739-14_5739-9del	rs72272981

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