List of variants in gene ATR reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp)	rs148064542	0.00041
NM_001184.4(ATR):c.2704T>C (p.Ser902Pro)	rs146202702	0.00036
NM_001184.4(ATR):c.4846T>G (p.Ser1616Ala)	rs201492267	0.00003
NM_001184.4(ATR):c.5303A>G (p.Asp1768Gly)	rs763130593	0.00001
NM_001184.4(ATR):c.7273C>T (p.Arg2425Ter)	rs1310011888	0.00001
NM_001184.4(ATR):c.3227A>G (p.His1076Arg)
NM_001184.4(ATR):c.4671G>A (p.Lys1557=)
NM_001184.4(ATR):c.4672C>G (p.His1558Asp)
NM_001184.4(ATR):c.4863G>A (p.Val1621=)
NM_001184.4(ATR):c.4891C>T (p.Arg1631Cys)
NM_001184.4(ATR):c.5078G>A (p.Ser1693Asn)	rs1375119564
NM_001184.4(ATR):c.5739-11_5739-4del	rs797045404
NM_001184.4(ATR):c.6460G>A (p.Asp2154Asn)

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