"Baylor Genetics"[submitter] AND "TH2LCRR"[gene] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2678148	NM_005732.4(RAD50):c.3429C>G (p.Ile1143Met)	TH2LCRR, RAD50 +1 more (I1143M)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder	GUncertain significance
Select item 480476	NM_005732.4(RAD50):c.3437T>C (p.Ile1146Thr)	RAD50, TH2-LCR +1 more (I1146T)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 482149	NM_005732.4(RAD50):c.3476del (p.Asp1159fs)	RAD50, TH2-LCR +1 more (D1159fs)	Deletion (frameshift variant +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GPathogenic/Likely pathogenic
Select item 142598	NM_005732.4(RAD50):c.3496C>T (p.Arg1166Trp)	TH2LCRR, RAD50 +1 more (R1166W)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder +4 more	GConflicting classifications of pathogenicity
Select item 230386	NM_005732.4(RAD50):c.3497G>T (p.Arg1166Leu)	RAD50, TH2-LCR +1 more (R1166L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 37378	NM_005732.4(RAD50):c.3508G>A (p.Asp1170Asn)	RAD50, TH2-LCR +1 more (D1170N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 230332	NM_005732.4(RAD50):c.3514A>T (p.Asn1172Tyr)	TH2-LCR, TH2LCRR +1 more (N1172Y)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480390	NM_005732.4(RAD50):c.3538C>T (p.Arg1180Trp)	TH2-LCR, TH2LCRR +1 more (R1180W)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 527386	NM_005732.4(RAD50):c.3539G>A (p.Arg1180Gln)	RAD50, TH2-LCR +1 more (R1180Q)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder +2 more	GUncertain significance
Select item 216097	NM_005732.4(RAD50):c.3553C>T (p.Arg1185Ter)	TH2LCRR, RAD50 +1 more (R1185*)	Single nucleotide variant (nonsense +1 more)	Nijmegen breakage syndrome-like disorder +2 more	GPathogenic
Select item 2678164	NM_005732.4(RAD50):c.3564dup (p.Leu1189fs)	RAD50, TH2-LCR +1 more (L1189fs)	Duplication (frameshift variant +1 more)	Nijmegen breakage syndrome-like disorder	GLikely pathogenic
Select item 2678150	NM_005732.4(RAD50):c.3565C>G (p.Leu1189Val)	RAD50, TH2-LCR +1 more (L1189V)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder	GUncertain significance
Select item 486234	NM_005732.4(RAD50):c.3592C>T (p.Arg1198Ter)	TH2LCRR, RAD50 +1 more (R1198*)	Single nucleotide variant (nonsense +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GPathogenic/Likely pathogenic
Select item 140973	NM_005732.4(RAD50):c.3593G>A (p.Arg1198Gln)	RAD50, TH2-LCR +1 more (R1198Q)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 184879	NM_005732.4(RAD50):c.3598C>T (p.Arg1200Ter)	RAD50, TH2-LCR +1 more (R1200*)	Single nucleotide variant (nonsense +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GPathogenic/Likely pathogenic
Select item 408396	NM_005732.4(RAD50):c.3612_3618+5del	RAD50, TH2-LCR +1 more	Deletion (non-coding transcript variant +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GLikely pathogenic
Select item 408358	NM_005732.4(RAD50):c.3625G>A (p.Ala1209Thr)	RAD50, TH2-LCR +1 more (A1209T)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 408382	NM_005732.4(RAD50):c.3641G>A (p.Arg1214His)	RAD50, TH2-LCR +1 more (R1214H)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 186088	NM_005732.4(RAD50):c.3641G>T (p.Arg1214Leu)	TH2LCRR, RAD50 +1 more (R1214L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 961102	NM_005732.4(RAD50):c.3655G>T (p.Glu1219Ter)	RAD50, TH2-LCR +1 more (E1219*)	Single nucleotide variant (nonsense)	Nijmegen breakage syndrome-like disorder +1 more	GPathogenic
Select item 240240	NM_005732.4(RAD50):c.3697C>A (p.Pro1233Thr)	RAD50, TH2-LCR +1 more (P1233T)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 230785	NM_005732.4(RAD50):c.3715C>T (p.Arg1239Ter)	RAD50, TH2-LCR +1 more (R1239*)	Single nucleotide variant (nonsense)	Nijmegen breakage syndrome-like disorder +2 more	GPathogenic/Likely pathogenic
Select item 140979	NM_005732.4(RAD50):c.3716G>A (p.Arg1239Gln)	RAD50, TH2-LCR +1 more (R1239Q)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 2678155	NM_005732.4(RAD50):c.3752+1G>A	RAD50, TH2-LCR +1 more	Single nucleotide variant (splice donor variant)	Nijmegen breakage syndrome-like disorder	GLikely pathogenic
Select item 480449	NM_005732.4(RAD50):c.3753-3C>G	RAD50, TH2-LCR +1 more	Single nucleotide variant (intron variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 2678147	NM_005732.4(RAD50):c.3753-2A>G	RAD50, TH2-LCR +1 more	Single nucleotide variant (splice acceptor variant)	Nijmegen breakage syndrome-like disorder	GLikely pathogenic
Select item 457468	NM_005732.4(RAD50):c.3753-1G>A	RAD50, TH2-LCR +1 more	Single nucleotide variant (splice acceptor variant)	Nijmegen breakage syndrome-like disorder +1 more	GLikely pathogenic
Select item 186665	NM_005732.4(RAD50):c.3767G>A (p.Arg1256His)	TH2LCRR, TH2-LCR +1 more (R1256H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 183984	NM_005732.4(RAD50):c.3769T>G (p.Ser1257Ala)	RAD50, TH2-LCR +1 more (S1257A)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 569669	NM_005732.4(RAD50):c.3776A>G (p.Gln1259Arg)	RAD50, TH2LCRR (Q1259R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 584476	NM_005732.4(RAD50):c.3779_3791dup (p.Leu1264_Leu1265insTer)	RAD50, TH2LCRR	Duplication (nonsense +2 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 457469	NM_005732.4(RAD50):c.3778C>T (p.Arg1260Cys)	RAD50, TH2LCRR (R1260C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 142065	NM_005732.4(RAD50):c.3779G>A (p.Arg1260His)	RAD50, TH2LCRR (R1260H)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 128022	NM_005732.4(RAD50):c.3789G>C (p.Gln1263His)	RAD50, TH2LCRR (Q1263H)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 482096	NM_005732.4(RAD50):c.3813_3815del (p.Glu1271del)	RAD50, TH2LCRR (E1271del)	Deletion (inframe_deletion +1 more)	Nijmegen breakage syndrome-like disorder +2 more	GUncertain significance
Select item 651404	NM_005732.4(RAD50):c.3816T>G (p.Asp1272Glu)	RAD50, TH2LCRR (D1272E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 142265	NM_005732.4(RAD50):c.3824A>G (p.Glu1275Gly)	RAD50, TH2LCRR (E1275G)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 184946	NM_005732.4(RAD50):c.3835C>T (p.Arg1279Cys)	RAD50, TH2LCRR (R1279C)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 841883	NM_005732.4(RAD50):c.3838T>C (p.Ser1280Pro)	RAD50, TH2LCRR (S1280P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 140919	NM_005732.4(RAD50):c.3857T>C (p.Phe1286Ser)	RAD50, TH2LCRR (F1286S)	Single nucleotide variant (missense variant +1 more)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance
Select item 567665	NM_005732.4(RAD50):c.3886T>A (p.Cys1296Ser)	RAD50, TH2LCRR (C1296S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480431	NM_005732.4(RAD50):c.3898G>A (p.Val1300Met)	RAD50, TH2LCRR (V1300M)	Single nucleotide variant (missense variant)	Nijmegen breakage syndrome-like disorder +1 more	GUncertain significance

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Items: 42