ClinVar Miner

List of variants in gene RPL9 studied for not provided

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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_000661.5(RPL9):c.162+90A>G rs2687958 0.66384
NM_000661.5(RPL9):c.366T>C (p.Tyr122=) rs2125313 0.66281
NM_000661.5(RPL9):c.472+92C>T rs1463478 0.44518
NM_000661.5(RPL9):c.392-71A>G rs10025155 0.20810
NM_000661.5(RPL9):c.391+169A>G rs1015450 0.15928
NM_000661.5(RPL9):c.258+52C>T rs2608830 0.15631
NM_000661.5(RPL9):c.258+175A>G rs2687957 0.15602
NM_000661.5(RPL9):c.391+16C>G rs28688785 0.05656
NM_000661.5(RPL9):c.-1-146_-1-145del rs79533777 0.03086
NM_000661.5(RPL9):c.405A>G (p.Ser135=) rs372055477 0.00025
NM_000661.5(RPL9):c.391+8C>T rs114111678 0.00022
NM_000661.5(RPL9):c.423A>G (p.Lys141=) rs193055808 0.00022
NM_000661.5(RPL9):c.20A>G (p.Asn7Ser) rs146928803 0.00010
NM_000661.5(RPL9):c.375G>C (p.Arg125Ser) rs145459909 0.00006
NM_000661.5(RPL9):c.162+17del rs759398193 0.00005
NM_000661.5(RPL9):c.163-8T>C rs775733169 0.00005
NM_000661.5(RPL9):c.59T>C (p.Leu20Pro) rs141176319 0.00005
NM_000661.5(RPL9):c.114C>T (p.Phe38=) rs147466054 0.00003
NM_000661.5(RPL9):c.207C>T (p.Thr69=) rs747523284 0.00003
NM_000661.5(RPL9):c.491C>T (p.Ala164Val) rs758145477 0.00003
NM_000661.5(RPL9):c.564G>T (p.Gln188His) rs748195496 0.00003
NM_000661.5(RPL9):c.10A>G (p.Ile4Val) rs771618498 0.00002
NM_000661.5(RPL9):c.219T>C (p.Ile73=) rs748553586 0.00002
NM_000661.5(RPL9):c.330T>G (p.Ser110=) rs757203996 0.00002
NM_000661.5(RPL9):c.116A>G (p.Asn39Ser) rs756847748 0.00001
NM_000661.5(RPL9):c.162+19A>G rs200724499 0.00001
NM_000661.5(RPL9):c.199C>T (p.Leu67=) rs1744161626 0.00001
NM_000661.5(RPL9):c.258+16A>G rs1197389980 0.00001
NM_000661.5(RPL9):c.270C>T (p.Tyr90=) rs768417540 0.00001
NM_000661.5(RPL9):c.283G>C (p.Val95Leu) rs372498694 0.00001
NM_000661.5(RPL9):c.379C>T (p.Arg127Trp) rs202000648 0.00001
NM_000661.5(RPL9):c.380G>A (p.Arg127Gln) rs1345812176 0.00001
NM_000661.5(RPL9):c.414A>G (p.Gln138=) rs200690365 0.00001
NM_000661.5(RPL9):c.46+9C>T rs777980650 0.00001
NM_000661.5(RPL9):c.47-11C>T rs754417283 0.00001
NM_000661.5(RPL9):c.472+16A>G rs1469388210 0.00001
NM_000661.5(RPL9):c.473-9C>T rs1744016653 0.00001
NM_000661.5(RPL9):c.568G>T (p.Ala190Ser) rs1453715995 0.00001
NM_000661.5(RPL9):c.71C>T (p.Thr24Ile) rs201850421 0.00001
NM_000661.5(RPL9):c.10A>C (p.Ile4Leu)
NM_000661.5(RPL9):c.114C>A (p.Phe38Leu) rs147466054
NM_000661.5(RPL9):c.160A>G (p.Arg54Gly) rs761909586
NM_000661.5(RPL9):c.162+3G>A rs2474981633
NM_000661.5(RPL9):c.163-9C>G rs2474980339
NM_000661.5(RPL9):c.166C>T (p.Arg56Trp)
NM_000661.5(RPL9):c.18C>T (p.Ser6=)
NM_000661.5(RPL9):c.19A>C (p.Asn7His)
NM_000661.5(RPL9):c.211C>A (p.Arg71=) rs1331263882
NM_000661.5(RPL9):c.212G>C (p.Arg71Pro) rs1744160516
NM_000661.5(RPL9):c.228T>C (p.His76=)
NM_000661.5(RPL9):c.231A>G (p.Val77=)
NM_000661.5(RPL9):c.245A>G (p.Lys82Arg) rs2474980219
NM_000661.5(RPL9):c.258+14T>C
NM_000661.5(RPL9):c.258+19C>A
NM_000661.5(RPL9):c.258+20T>G rs2474980166
NM_000661.5(RPL9):c.259-10_259-7del rs142648868
NM_000661.5(RPL9):c.259-14T>C rs1430628276
NM_000661.5(RPL9):c.259-5C>T rs745731738
NM_000661.5(RPL9):c.307G>A (p.Val103Ile)
NM_000661.5(RPL9):c.344G>A (p.Arg115Gln)
NM_000661.5(RPL9):c.391+155_391+156insC rs3216720
NM_000661.5(RPL9):c.391+16C>T rs28688785
NM_000661.5(RPL9):c.392-11T>C
NM_000661.5(RPL9):c.392-12C>T rs778833788
NM_000661.5(RPL9):c.414A>C (p.Gln138His) rs200690365
NM_000661.5(RPL9):c.430T>A (p.Leu144Ile)
NM_000661.5(RPL9):c.452T>C (p.Ile151Thr)
NM_000661.5(RPL9):c.462T>G (p.Val154=) rs1412359099
NM_000661.5(RPL9):c.47-4C>G
NM_000661.5(RPL9):c.47-9C>G
NM_000661.5(RPL9):c.473-3T>A
NM_000661.5(RPL9):c.48C>T (p.Val16=) rs767101796
NM_000661.5(RPL9):c.537C>A (p.Ile179=)
NM_000661.5(RPL9):c.570T>C (p.Ala190=) rs779414751
NM_000661.5(RPL9):c.578A>G (p.Ter193=) rs2474974257
NM_000661.5(RPL9):c.72A>G (p.Thr24=) rs772175387
NM_000661.5(RPL9):c.98C>T (p.Thr33Ile)

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