ClinVar Miner

List of variants in gene ATR studied for not provided

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Gene type:
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Total variants: 124
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HGVS dbSNP
NM_001184.4(ATR):c.1170+148_1170+149insA
NM_001184.4(ATR):c.1170+150_1170+151insA
NM_001184.4(ATR):c.117A>G (p.Gln39=)
NM_001184.4(ATR):c.1221C>A (p.Ile407=)
NM_001184.4(ATR):c.1308G>A (p.Ser436=)
NM_001184.4(ATR):c.1326A>G (p.Lys442=) rs28897765
NM_001184.4(ATR):c.1328G>C (p.Arg443Thr) rs28367453
NM_001184.4(ATR):c.1335A>G (p.Pro445=)
NM_001184.4(ATR):c.1349+289A>G
NM_001184.4(ATR):c.1350-4A>G
NM_001184.4(ATR):c.1358_1359del (p.His453fs) rs886044646
NM_001184.4(ATR):c.1411G>C (p.Glu471Gln)
NM_001184.4(ATR):c.151+72G>A
NM_001184.4(ATR):c.152-10A>T
NM_001184.4(ATR):c.1608A>G (p.Ser536=)
NM_001184.4(ATR):c.1609T>C (p.Leu537=)
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930
NM_001184.4(ATR):c.1878T>C (p.Asp626=)
NM_001184.4(ATR):c.1885+7G>A rs74282951
NM_001184.4(ATR):c.190A>G (p.Thr64Ala) rs35306038
NM_001184.4(ATR):c.1950G>A (p.Glu650=) rs28910270
NM_001184.4(ATR):c.195C>T (p.Ser65=) rs139304565
NM_001184.4(ATR):c.2157C>T (p.His719=) rs150161871
NM_001184.4(ATR):c.2205C>T (p.His735=) rs148955716
NM_001184.4(ATR):c.2226T>C (p.Cys742=) rs147895945
NM_001184.4(ATR):c.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2341+185G>A
NM_001184.4(ATR):c.2342-175A>G
NM_001184.4(ATR):c.2634-74C>T
NM_001184.4(ATR):c.2664A>G (p.Ala888=)
NM_001184.4(ATR):c.2688G>A (p.Leu896=) rs117926957
NM_001184.4(ATR):c.268C>T (p.His90Tyr) rs28897763
NM_001184.4(ATR):c.2691A>G (p.Leu897=)
NM_001184.4(ATR):c.276C>G (p.Ala92=)
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863
NM_001184.4(ATR):c.2805+272T>G
NM_001184.4(ATR):c.2806-4C>T
NM_001184.4(ATR):c.2844A>C (p.Ala948=) rs147286949
NM_001184.4(ATR):c.2875G>A (p.Val959Met) rs28910271
NM_001184.4(ATR):c.289A>T (p.Ile97Phe) rs138473993
NM_001184.4(ATR):c.2922G>A (p.Thr974=)
NM_001184.4(ATR):c.293-20C>T rs115097590
NM_001184.4(ATR):c.2992C>T (p.Leu998=)
NM_001184.4(ATR):c.303T>C (p.Asn101=)
NM_001184.4(ATR):c.305G>T (p.Trp102Leu) rs794727632
NM_001184.4(ATR):c.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3171+132A>G
NM_001184.4(ATR):c.3171+1G>A rs199731535
NM_001184.4(ATR):c.325C>T (p.Arg109Trp) rs146405935
NM_001184.4(ATR):c.3372A>G (p.Gln1124=)
NM_001184.4(ATR):c.3433A>G (p.Ile1145Val)
NM_001184.4(ATR):c.3451-4A>G
NM_001184.4(ATR):c.3582-302T>C
NM_001184.4(ATR):c.3702C>T (p.Phe1234=)
NM_001184.4(ATR):c.3726-47A>G rs73240314
NM_001184.4(ATR):c.3891C>T (p.Val1297=)
NM_001184.4(ATR):c.3894T>C (p.Asp1298=)
NM_001184.4(ATR):c.3963T>C (p.Tyr1321=)
NM_001184.4(ATR):c.4002G>A (p.Gln1334=) rs56026468
NM_001184.4(ATR):c.4153-10del rs112116713
NM_001184.4(ATR):c.4153-21dup rs112116713
NM_001184.4(ATR):c.423T>C (p.Ile141=) rs10935466
NM_001184.4(ATR):c.4266+120A>T
NM_001184.4(ATR):c.4323A>G (p.Gln1441=) rs56100509
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.4376A>G (p.Asn1459Ser) rs144591613
NM_001184.4(ATR):c.437C>A (p.Thr146Lys) rs368592452
NM_001184.4(ATR):c.4383-177C>T
NM_001184.4(ATR):c.4383-232G>T
NM_001184.4(ATR):c.4398G>A (p.Gln1466=)
NM_001184.4(ATR):c.4405A>G (p.Thr1469Ala) rs78895258
NM_001184.4(ATR):c.4503+247A>G
NM_001184.4(ATR):c.4504-263T>A
NM_001184.4(ATR):c.4509A>T (p.Arg1503=) rs398123602
NM_001184.4(ATR):c.4575C>T (p.Thr1525=)
NM_001184.4(ATR):c.4641+9A>G rs369284360
NM_001184.4(ATR):c.4677C>T (p.Asp1559=) rs112726878
NM_001184.4(ATR):c.4764C>T (p.Leu1588=) rs142240637
NM_001184.4(ATR):c.4820G>A (p.Ser1607Asn) rs55724025
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265
NM_001184.4(ATR):c.4846T>G (p.Ser1616Ala) rs201492267
NM_001184.4(ATR):c.4852+256T>C
NM_001184.4(ATR):c.5070C>T (p.Ala1690=)
NM_001184.4(ATR):c.5094A>G (p.Ala1698=)
NM_001184.4(ATR):c.5196+109G>A
NM_001184.4(ATR):c.5197-289A>G
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931
NM_001184.4(ATR):c.5288+130G>A
NM_001184.4(ATR):c.5288+248T>C
NM_001184.4(ATR):c.5380+121C>A
NM_001184.4(ATR):c.5381-41C>T rs34502778
NM_001184.4(ATR):c.5601T>C (p.Leu1867=) rs138891875
NM_001184.4(ATR):c.5739-11_5739-4del rs797045404
NM_001184.4(ATR):c.5739-14_5739-7del rs878853001
NM_001184.4(ATR):c.5739-14_5739-9del rs72272981
NM_001184.4(ATR):c.5739-7_5739-6del rs72371423
NM_001184.4(ATR):c.5900G>A (p.Gly1967Asp) rs751198306
NM_001184.4(ATR):c.5931A>G (p.Gln1977=) rs150964938
NM_001184.4(ATR):c.5987T>C (p.Met1996Thr) rs150339560
NM_001184.4(ATR):c.60-51A>T
NM_001184.4(ATR):c.6087C>T (p.Thr2029=)
NM_001184.4(ATR):c.6126T>C (p.Leu2042=)
NM_001184.4(ATR):c.6339A>G (p.Val2113=) rs7635479
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273
NM_001184.4(ATR):c.6687+262A>G
NM_001184.4(ATR):c.6726T>C (p.His2242=)
NM_001184.4(ATR):c.6903A>G (p.Glu2301=)
NM_001184.4(ATR):c.7041+8G>A rs201106004
NM_001184.4(ATR):c.7274G>A (p.Arg2425Gln) rs2229032
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295
NM_001184.4(ATR):c.7407T>C (p.Tyr2469=)
NM_001184.4(ATR):c.7411C>T (p.Leu2471=)
NM_001184.4(ATR):c.7479A>G (p.Val2493=)
NM_001184.4(ATR):c.7488T>C (p.Asn2496=)
NM_001184.4(ATR):c.7632T>A (p.Arg2544=)
NM_001184.4(ATR):c.7655+169A>C
NM_001184.4(ATR):c.7667C>G (p.Thr2556Ser) rs200490116
NM_001184.4(ATR):c.7762-174A>G
NM_001184.4(ATR):c.7800A>G (p.Gln2600=)
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904
NM_001184.4(ATR):c.7902C>T (p.Cys2634=)
NM_001184.4(ATR):c.816A>G (p.Ser272=) rs34685245
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448
NM_001184.4(ATR):c.993C>T (p.Asp331=)

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