ClinVar Miner

List of variants in gene RPS19 studied for not provided

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001022.4(RPS19):c.356+14= rs1366610 0.99999
NM_001022.4(RPS19):c.-1+36= rs930102 0.57140
NM_001022.4(RPS19):c.-1+94C>G rs61761218 0.00510
NM_001022.4(RPS19):c.411+12G>A rs61762296 0.00287
NM_001022.4(RPS19):c.-1+26G>T rs74449035 0.00283
NM_001022.4(RPS19):c.412-131T>C rs187990365 0.00215
NM_001022.4(RPS19):c.60C>G (p.Ala20=) rs149249194 0.00108
NM_001022.4(RPS19):c.164C>T (p.Thr55Met) rs147508369 0.00039
NM_001022.4(RPS19):c.68A>G (p.Lys23Arg) rs143477104 0.00028
NM_001022.3(RPS19):c.-167C>T rs578174704 0.00017
NM_001022.4(RPS19):c.-33C>T rs561259640 0.00009
NM_001022.4(RPS19):c.356+13G>C rs781957086 0.00008
NM_001022.4(RPS19):c.208G>A (p.Ala70Thr) rs782368794 0.00006
NM_001022.4(RPS19):c.72-17C>G rs150151184 0.00005
NM_001022.4(RPS19):c.411+6G>C rs138397598 0.00003
NC_000019.10:g.41860144_41860145insGCCA rs34020014
NM_001022.3(RPS19):c.-137C>T rs2074010327
NM_001022.3(RPS19):c.-180C>T rs1465805886
NM_001022.4(RPS19):c.105dup (p.Thr36fs) rs1555839154
NM_001022.4(RPS19):c.115C>G (p.Leu39Val)
NM_001022.4(RPS19):c.128_129del (p.Lys43fs) rs1555839161
NM_001022.4(RPS19):c.131_132del (p.Glu44fs) rs2074027448
NM_001022.4(RPS19):c.139C>T (p.Pro47Ser) rs1064793253
NM_001022.4(RPS19):c.166C>G (p.Arg56Gly) rs2513667436
NM_001022.4(RPS19):c.172+907A>G rs61761229
NM_001022.4(RPS19):c.173-3del rs2513682812
NM_001022.4(RPS19):c.178A>C (p.Thr60Pro) rs782637049
NM_001022.4(RPS19):c.184C>T (p.Arg62Trp) rs104894711
NM_001022.4(RPS19):c.185G>A (p.Arg62Gln) rs1555841301
NM_001022.4(RPS19):c.200G>C (p.Arg67Pro) rs963817249
NM_001022.4(RPS19):c.208G>T (p.Ala70Ser)
NM_001022.4(RPS19):c.280C>T (p.Arg94Ter) rs61762293
NM_001022.4(RPS19):c.302G>A (p.Arg101His) rs2123284131
NM_001022.4(RPS19):c.302G>C (p.Arg101Pro) rs2123284131
NM_001022.4(RPS19):c.308T>A (p.Val103Asp) rs1131691437
NM_001022.4(RPS19):c.335TGG[1] (p.Val113del) rs1064794604
NM_001022.4(RPS19):c.351A>G (p.Gln117=) rs2513683440
NM_001022.4(RPS19):c.356+18G>C rs61762294
NM_001022.4(RPS19):c.372dup (p.Pro125fs) rs2074126900
NM_001022.4(RPS19):c.384_385del (p.Asp130fs) rs869066130
NM_001022.4(RPS19):c.3G>T (p.Met1Ile) rs138938035
NM_001022.4(RPS19):c.406G>T (p.Gly136Ter) rs144337183
NM_001022.4(RPS19):c.411+2T>C rs1555841598
NM_001022.4(RPS19):c.412-8_412-1dup rs2123290691
NM_001022.4(RPS19):c.422C>T (p.Ala141Val) rs2123290729
NM_001022.4(RPS19):c.43G>T (p.Val15Phe) rs104894717
NM_001022.4(RPS19):c.49G>C (p.Ala17Pro) rs782329429
NM_001022.4(RPS19):c.72-1G>C rs146366047
NM_001022.4(RPS19):c.94G>T (p.Glu32Ter) rs2513667169

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