ClinVar Miner

List of variants in gene CSRP3 studied for not specified

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Gene type:
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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_003476.5(CSRP3):c.336G>A (p.Ala112=) rs13451 0.07238
NM_003476.5(CSRP3):c.150G>A (p.Ala50=) rs7124801 0.03207
NM_003476.5(CSRP3):c.312C>G (p.Thr104=) rs45582433 0.01721
NM_003476.5(CSRP3):c.415-30T>C rs7103779 0.01252
NM_003476.5(CSRP3):c.213C>T (p.Ile71=) rs45476991 0.00499
NM_003476.5(CSRP3):c.508+18C>T rs144404101 0.00332
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg) rs45550635 0.00271
NM_003476.5(CSRP3):c.*12G>A rs45607943 0.00108
NM_003476.5(CSRP3):c.162G>A (p.Ser54=) rs112848043 0.00104
NM_003476.5(CSRP3):c.299G>A (p.Arg100His) rs138218523 0.00097
NM_003476.4(CSRP3):c.-74A>C rs45498797 0.00092
NM_003476.5(CSRP3):c.-46C>T rs373296490 0.00033
NM_003476.5(CSRP3):c.175A>G (p.Lys59Glu) rs769003538 0.00016
NM_003476.5(CSRP3):c.544G>C (p.Gly182Arg) rs111868331 0.00011
NM_003476.5(CSRP3):c.272A>T (p.Gln91Leu) rs727504436 0.00009
NM_003476.5(CSRP3):c.379G>A (p.Val127Ile) rs149201422 0.00009
NM_003476.5(CSRP3):c.49G>A (p.Val17Ile) rs767932680 0.00009
NM_003476.5(CSRP3):c.131T>C (p.Leu44Pro) rs104894205 0.00006
NM_003476.5(CSRP3):c.148G>A (p.Ala50Thr) rs145300736 0.00006
NM_003476.5(CSRP3):c.16G>A (p.Gly6Arg) rs185980145 0.00006
NM_003476.5(CSRP3):c.294G>A (p.Pro98=) rs142832902 0.00006
NM_003476.5(CSRP3):c.136A>C (p.Ser46Arg) rs137852765 0.00005
NM_003476.5(CSRP3):c.535A>G (p.Thr179Ala) rs397516859 0.00005
NM_003476.3(CSRP3):c.-226G>A rs1057523542 0.00004
NM_003476.5(CSRP3):c.-28-9T>A rs1053281170 0.00004
NM_003476.5(CSRP3):c.230C>G (p.Ala77Gly) rs772138289 0.00004
NM_003476.5(CSRP3):c.536C>T (p.Thr179Met) rs142019584 0.00004
NM_003476.5(CSRP3):c.-3A>C rs760384315 0.00003
NM_003476.5(CSRP3):c.140C>T (p.Thr47Met) rs397516851 0.00003
NM_003476.5(CSRP3):c.191G>A (p.Arg64His) rs375014380 0.00003
NM_003476.5(CSRP3):c.282-16C>A rs757074408 0.00003
NM_003476.5(CSRP3):c.327A>G (p.Lys109=) rs778512127 0.00003
NM_003476.5(CSRP3):c.252G>A (p.Thr84=) rs755614464 0.00002
NM_003476.5(CSRP3):c.282-16C>T rs757074408 0.00002
NM_003476.5(CSRP3):c.437G>A (p.Arg146His) rs377066670 0.00002
NM_003476.3(CSRP3):c.-236G>C rs1057524085 0.00001
NM_003476.4(CSRP3):c.-70C>T rs147388951 0.00001
NM_003476.5(CSRP3):c.-54G>T rs1057523459 0.00001
NM_003476.5(CSRP3):c.141G>A (p.Thr47=) rs758842207 0.00001
NM_003476.5(CSRP3):c.152C>A (p.Ala51Asp) rs397516853 0.00001
NM_003476.5(CSRP3):c.197A>G (p.Tyr66Cys) rs397516854 0.00001
NM_003476.5(CSRP3):c.255C>T (p.Gly85=) rs752338221 0.00001
NM_003476.5(CSRP3):c.261T>C (p.His87=) rs773476497 0.00001
NM_003476.5(CSRP3):c.449G>A (p.Cys150Tyr) rs761507504 0.00001
NM_003476.5(CSRP3):c.509-16C>T rs371700321 0.00001
NM_003476.5(CSRP3):c.516T>C (p.Tyr172=) rs727504575 0.00001
NM_003476.4(CSRP3):c.-84A>G rs727504617
NM_003476.4(CSRP3):c.-88A>G rs727502947
NM_003476.5(CSRP3):c.108C>T (p.His36=) rs763193066
NM_003476.5(CSRP3):c.116C>A (p.Ala39Asp) rs748417030
NM_003476.5(CSRP3):c.118T>G (p.Cys40Gly)
NM_003476.5(CSRP3):c.147C>A (p.Val49=) rs576346189
NM_003476.5(CSRP3):c.174C>T (p.Cys58=) rs1057520959
NM_003476.5(CSRP3):c.219T>C (p.Tyr73=) rs397516852
NM_003476.5(CSRP3):c.265G>A (p.Gly89Ser) rs367827746
NM_003476.5(CSRP3):c.282-5_285del rs397516855
NM_003476.5(CSRP3):c.282G>T (p.Gln94His) rs550097061
NM_003476.5(CSRP3):c.334G>C (p.Ala112Pro) rs727504905
NM_003476.5(CSRP3):c.354G>C (p.Glu118Asp) rs876657767
NM_003476.5(CSRP3):c.456G>A (p.Lys152=) rs397516856
NM_003476.5(CSRP3):c.465G>T (p.Glu155Asp) rs200334242
NM_003476.5(CSRP3):c.47C>T (p.Thr16Ile) rs397516857
NM_003476.5(CSRP3):c.508+17A>T rs373822409
NM_003476.5(CSRP3):c.508+9T>C rs727504517
NM_003476.5(CSRP3):c.508G>T (p.Val170Phe) rs757433657
NM_003476.5(CSRP3):c.509-20C>A rs375020550
NM_003476.5(CSRP3):c.509-20C>T
NM_003476.5(CSRP3):c.509-3_509-2del rs397516858
NM_003476.5(CSRP3):c.539G>T (p.Gly180Val) rs727504899
NM_003476.5(CSRP3):c.579_582del (p.Lys193fs) rs727502946

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