ClinVar Miner

List of variants in gene STING1 reported as uncertain significance for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 142
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HGVS dbSNP gnomAD frequency
NM_198282.4(STING1):c.784G>A (p.Ala262Thr) rs140038439 0.00032
NM_198282.4(STING1):c.1076A>G (p.Gln359Arg) rs141830680 0.00023
NM_198282.4(STING1):c.575G>T (p.Gly192Val) rs201096097 0.00019
NM_198282.4(STING1):c.758G>A (p.Arg253Gln) rs148833313 0.00018
NM_198282.4(STING1):c.142G>T (p.Val48Leu) rs902177158 0.00009
NM_198282.4(STING1):c.929G>A (p.Arg310His) rs144683867 0.00009
NM_198282.4(STING1):c.757C>T (p.Arg253Trp) rs199795457 0.00006
NM_198282.4(STING1):c.760-3T>C rs759930084 0.00006
NM_198282.4(STING1):c.761C>T (p.Ala254Val) rs774690247 0.00006
NM_198282.4(STING1):c.992G>A (p.Arg331Gln) rs370524913 0.00006
NM_198282.4(STING1):c.32C>T (p.Pro11Leu) rs146423746 0.00004
NM_198282.4(STING1):c.548A>G (p.Asn183Ser) rs201277595 0.00004
NM_198282.4(STING1):c.1000C>T (p.Arg334Trp) rs1197819878 0.00003
NM_198282.4(STING1):c.503T>C (p.Leu168Pro) rs532530144 0.00003
NM_198282.4(STING1):c.688G>A (p.Gly230Ser) rs370230460 0.00003
NM_198282.4(STING1):c.1001G>A (p.Arg334Gln) rs758939417 0.00002
NM_198282.4(STING1):c.1006G>A (p.Glu336Lys) rs1268179693 0.00002
NM_198282.4(STING1):c.1049C>T (p.Ala350Val) rs143322684 0.00002
NM_198282.4(STING1):c.1127C>T (p.Thr376Met) rs370381358 0.00002
NM_198282.4(STING1):c.134G>A (p.Arg45Gln) rs762935025 0.00002
NM_198282.4(STING1):c.589C>T (p.Arg197Trp) rs763892914 0.00002
NM_198282.4(STING1):c.637A>C (p.Ser213Arg) rs1342489613 0.00002
NM_198282.4(STING1):c.668A>G (p.Asp223Gly) rs746097569 0.00002
NM_198282.4(STING1):c.1003C>A (p.Gln335Lys) rs1254726825 0.00001
NM_198282.4(STING1):c.1054C>T (p.Pro352Ser) rs977753165 0.00001
NM_198282.4(STING1):c.1123C>T (p.Arg375Cys) rs144606267 0.00001
NM_198282.4(STING1):c.161T>C (p.Leu54Pro) rs1292788155 0.00001
NM_198282.4(STING1):c.184G>A (p.Gly62Arg) rs766819764 0.00001
NM_198282.4(STING1):c.211C>A (p.Arg71Ser) rs768649460 0.00001
NM_198282.4(STING1):c.233G>A (p.Arg78Gln) rs11554775 0.00001
NM_198282.4(STING1):c.26C>T (p.Ser9Phe) rs888652949 0.00001
NM_198282.4(STING1):c.2T>C (p.Met1Thr) rs754838823 0.00001
NM_198282.4(STING1):c.40A>C (p.Arg14=) rs761439213 0.00001
NM_198282.4(STING1):c.418G>A (p.Ala140Thr) rs1370637313 0.00001
NM_198282.4(STING1):c.430A>G (p.Ile144Val) rs755245286 0.00001
NM_198282.4(STING1):c.493A>G (p.Ile165Val) rs768359336 0.00001
NM_198282.4(STING1):c.49G>A (p.Gly17Arg) rs759944012 0.00001
NM_198282.4(STING1):c.4C>T (p.Pro2Ser) rs1223377482 0.00001
NM_198282.4(STING1):c.532C>T (p.Arg178Trp) rs1240603758 0.00001
NM_198282.4(STING1):c.539G>A (p.Arg180Gln) rs759123296 0.00001
NM_198282.4(STING1):c.547A>C (p.Asn183His) rs773990834 0.00001
NM_198282.4(STING1):c.572G>A (p.Arg191Gln) rs750561744 0.00001
NM_198282.4(STING1):c.590G>A (p.Arg197Gln) rs760564156 0.00001
NM_198282.4(STING1):c.697G>A (p.Ala233Thr) rs201670175 0.00001
NM_198282.4(STING1):c.709G>T (p.Asp237Tyr) rs1291110297 0.00001
NM_198282.4(STING1):c.751G>A (p.Gly251Arg) rs1409697347 0.00001
NM_198282.4(STING1):c.767C>T (p.Thr256Ile) rs769794754 0.00001
NM_198282.4(STING1):c.841C>T (p.Arg281Trp) rs750077345 0.00001
NM_198282.4(STING1):c.946+1G>T rs375560052 0.00001
NC_000005.10:g.(?_139476241)_(139481724_?)dup
NC_000005.9:g.(?_138855826)_(138861309_?)del
NC_000005.9:g.(?_138855846)_(138858113_?)del
NM_198282.4(STING1):c.1013del (p.Lys338fs) rs765347385
NM_198282.4(STING1):c.1015G>A (p.Glu339Lys) rs1751660621
NM_198282.4(STING1):c.1021G>C (p.Val341Leu) rs1751660369
NM_198282.4(STING1):c.1025C>A (p.Thr342Asn)
NM_198282.4(STING1):c.1025del (p.Thr342fs) rs1581447916
NM_198282.4(STING1):c.1027G>A (p.Val343Met)
NM_198282.4(STING1):c.1028T>C (p.Val343Ala)
NM_198282.4(STING1):c.102G>C (p.Trp34Cys)
NM_198282.4(STING1):c.1061C>A (p.Thr354Asn)
NM_198282.4(STING1):c.1061C>T (p.Thr354Ile)
NM_198282.4(STING1):c.1084G>A (p.Glu362Lys)
NM_198282.4(STING1):c.1124G>A (p.Arg375His) rs117897081
NM_198282.4(STING1):c.1127C>G (p.Thr376Arg) rs370381358
NM_198282.4(STING1):c.1129G>T (p.Asp377Tyr) rs1368968919
NM_198282.4(STING1):c.125A>C (p.His42Pro)
NM_198282.4(STING1):c.128C>T (p.Thr43Ile)
NM_198282.4(STING1):c.133C>T (p.Arg45Trp)
NM_198282.4(STING1):c.170G>T (p.Gly57Val)
NM_198282.4(STING1):c.211C>T (p.Arg71Cys)
NM_198282.4(STING1):c.212_213delinsAA (p.Arg71Gln) rs1751847315
NM_198282.4(STING1):c.21T>G (p.His7Gln)
NM_198282.4(STING1):c.220C>T (p.His74Tyr) rs745727679
NM_198282.4(STING1):c.227+1G>A rs1751846731
NM_198282.4(STING1):c.227+4A>G rs2152094440
NM_198282.4(STING1):c.228-3C>T rs1751840868
NM_198282.4(STING1):c.233G>C (p.Arg78Pro) rs11554775
NM_198282.4(STING1):c.40del (p.Arg14fs)
NM_198282.4(STING1):c.428A>C (p.Glu143Ala)
NM_198282.4(STING1):c.42G>A (p.Arg14=)
NM_198282.4(STING1):c.44dup (p.His16fs) rs1581455186
NM_198282.4(STING1):c.479C>T (p.Ala160Val) rs767904008
NM_198282.4(STING1):c.493A>C (p.Ile165Leu) rs768359336
NM_198282.4(STING1):c.496G>T (p.Gly166Ter)
NM_198282.4(STING1):c.498A>G (p.Gly166=)
NM_198282.4(STING1):c.505C>T (p.Arg169Trp)
NM_198282.4(STING1):c.520G>A (p.Glu174Lys)
NM_198282.4(STING1):c.524T>C (p.Leu175Pro)
NM_198282.4(STING1):c.529G>A (p.Ala177Thr) rs2152093638
NM_198282.4(STING1):c.533G>A (p.Arg178Gln)
NM_198282.4(STING1):c.538C>T (p.Arg180Ter)
NM_198282.4(STING1):c.545A>C (p.Tyr182Ser)
NM_198282.4(STING1):c.551A>T (p.Gln184Leu)
NM_198282.4(STING1):c.5C>T (p.Pro2Leu)
NM_198282.4(STING1):c.602T>C (p.Leu201Pro) rs1581450494
NM_198282.4(STING1):c.61_64del (p.Ala21fs)
NM_198282.4(STING1):c.620G>A (p.Gly207Glu)
NM_198282.4(STING1):c.620G>T (p.Gly207Val)
NM_198282.4(STING1):c.622G>A (p.Val208Met)
NM_198282.4(STING1):c.658C>T (p.Arg220Cys)
NM_198282.4(STING1):c.65C>A (p.Ala22Asp)
NM_198282.4(STING1):c.688G>T (p.Gly230Cys)
NM_198282.4(STING1):c.688_689delinsTC (p.Gly230Ser) rs1751724669
NM_198282.4(STING1):c.691G>A (p.Asp231Asn)
NM_198282.4(STING1):c.695_696insGTGACCG (p.His232delinsGlnTer)
NM_198282.4(STING1):c.69G>C (p.Leu23Phe)
NM_198282.4(STING1):c.70G>T (p.Val24Phe)
NM_198282.4(STING1):c.710A>G (p.Asp237Gly) rs1167471683
NM_198282.4(STING1):c.722G>C (p.Ser241Thr)
NM_198282.4(STING1):c.755A>G (p.Gln252Arg)
NM_198282.4(STING1):c.759+3A>G
NM_198282.4(STING1):c.760-2_766delinsTACCT rs2152093375
NM_198282.4(STING1):c.777G>A (p.Leu259=)
NM_198282.4(STING1):c.785C>G (p.Ala262Gly) rs2152093371
NM_198282.4(STING1):c.790C>T (p.Pro264Ser) rs141928874
NM_198282.4(STING1):c.7C>T (p.His3Tyr) rs1490896074
NM_198282.4(STING1):c.804G>C (p.Leu268Phe) rs2152093364
NM_198282.4(STING1):c.808G>A (p.Ala270Thr)
NM_198282.4(STING1):c.826C>G (p.Gln276Glu)
NM_198282.4(STING1):c.844G>A (p.Glu282Lys)
NM_198282.4(STING1):c.845A>G (p.Glu282Gly) rs1483629542
NM_198282.4(STING1):c.847G>A (p.Asp283Asn)
NM_198282.4(STING1):c.851G>A (p.Arg284Lys)
NM_198282.4(STING1):c.856G>A (p.Glu286Lys)
NM_198282.4(STING1):c.862G>A (p.Ala288Thr)
NM_198282.4(STING1):c.908C>A (p.Pro303His)
NM_198282.4(STING1):c.91G>T (p.Val31Leu)
NM_198282.4(STING1):c.92T>C (p.Val31Ala) rs1321304491
NM_198282.4(STING1):c.931C>T (p.Leu311Phe)
NM_198282.4(STING1):c.932T>C (p.Leu311Pro)
NM_198282.4(STING1):c.946+5G>A
NM_198282.4(STING1):c.946+5G>T
NM_198282.4(STING1):c.946+6G>A
NM_198282.4(STING1):c.946+6G>C
NM_198282.4(STING1):c.947-3C>T
NM_198282.4(STING1):c.952G>C (p.Ala318Pro)
NM_198282.4(STING1):c.952G>T (p.Ala318Ser) rs1561482019
NM_198282.4(STING1):c.95C>T (p.Thr32Ile)
NM_198282.4(STING1):c.979C>A (p.Gln327Lys) rs201015563
NM_198282.4(STING1):c.980A>C (p.Gln327Pro)
NM_198282.4(STING1):c.991C>T (p.Arg331Trp)

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