List of variants in gene ATR reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
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.293-20C>T	rs115097590	0.01504
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.3120G>A (p.Leu1040=)	rs28910272
NM_001184.4(ATR):c.5739-14_5739-9del	rs72272981

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