ClinVar Miner

List of variants in gene RP2 reported as likely benign for not provided

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_006915.3(RP2):c.844C>T (p.Arg282Trp) rs1805147 0.01917
NM_006915.3(RP2):c.260C>T (p.Thr87Ile) rs147783915 0.00496
NM_006915.3(RP2):c.431A>G (p.Lys144Arg) rs3126141 0.00008
NM_006915.3(RP2):c.650A>G (p.Asn217Ser) rs781878275 0.00007
NM_006915.3(RP2):c.102+13G>C rs371530596 0.00005
NM_006915.3(RP2):c.102+19C>A rs374569197 0.00005
NM_006915.3(RP2):c.285C>G (p.Pro95=) rs374743004 0.00005
NM_006915.3(RP2):c.970-9T>G rs2519930051 0.00004
NM_006915.3(RP2):c.807A>G (p.Glu269=) rs148517937 0.00003
NM_006915.3(RP2):c.1026C>T (p.Asn342=) rs782305404 0.00002
NM_006915.3(RP2):c.103-16T>A rs1346406616 0.00002
NM_006915.3(RP2):c.298G>A (p.Val100Met) rs781936550 0.00002
NM_006915.3(RP2):c.593A>G (p.Tyr198Cys) rs782195010 0.00002
NM_006915.3(RP2):c.750C>T (p.Ala250=) rs782562995 0.00002
NM_006915.3(RP2):c.949G>A (p.Glu317Lys) rs782721235 0.00002
NM_006915.3(RP2):c.969+18C>G rs369210778 0.00002
NM_006915.3(RP2):c.102+17A>G rs1188012124 0.00001
NM_006915.3(RP2):c.122T>C (p.Met41Thr) rs782356034 0.00001
NM_006915.3(RP2):c.167C>T (p.Thr56Met) rs1201646093 0.00001
NM_006915.3(RP2):c.333A>G (p.Thr111=) rs1924901769 0.00001
NM_006915.3(RP2):c.366T>C (p.Cys122=) rs1924903665 0.00001
NM_006915.3(RP2):c.396C>G (p.Ala132=) rs372910103 0.00001
NM_006915.3(RP2):c.621C>G (p.Leu207=) rs782093466 0.00001
NM_006915.3(RP2):c.632G>A (p.Arg211His) rs782164955 0.00001
NM_006915.3(RP2):c.768+13A>G rs1284693367 0.00001
NM_006915.3(RP2):c.883+19G>A rs1415120873 0.00001
NM_006915.3(RP2):c.912G>A (p.Gly304=) rs1925390675 0.00001
NM_006915.3(RP2):c.948C>T (p.Asn316=) rs1170818854 0.00001
NM_006915.3(RP2):c.96C>G (p.Arg32=) rs2519902183 0.00001
NM_006915.3(RP2):c.102+13G>T rs371530596
NM_006915.3(RP2):c.102+14T>A
NM_006915.3(RP2):c.102+20C>T rs2519902228
NM_006915.3(RP2):c.1032T>C (p.Ala344=) rs2519930160
NM_006915.3(RP2):c.168G>A (p.Thr56=) rs371935908
NM_006915.3(RP2):c.180A>G (p.Gln60=) rs2519913861
NM_006915.3(RP2):c.207C>T (p.Asn69=) rs1556318560
NM_006915.3(RP2):c.285C>T (p.Pro95=) rs374743004
NM_006915.3(RP2):c.354T>C (p.Arg118=) rs1035661138
NM_006915.3(RP2):c.429C>A (p.Ile143=) rs2519914406
NM_006915.3(RP2):c.447A>G (p.Gln149=) rs1556318656
NM_006915.3(RP2):c.489G>A (p.Gly163=) rs2519914493
NM_006915.3(RP2):c.507T>C (p.Asn169=)
NM_006915.3(RP2):c.564T>C (p.Leu188=) rs1556318678
NM_006915.3(RP2):c.576T>C (p.Asp192=) rs2519914618
NM_006915.3(RP2):c.681G>A (p.Gln227=) rs1924913666
NM_006915.3(RP2):c.702A>G (p.Glu234=) rs1924914203
NM_006915.3(RP2):c.705A>G (p.Ser235=)
NM_006915.3(RP2):c.717A>G (p.Val239=) rs1556318741
NM_006915.3(RP2):c.720A>G (p.Leu240=) rs1556318748
NM_006915.3(RP2):c.768+12G>A rs1316569237
NM_006915.3(RP2):c.768+12G>C rs1316569237
NM_006915.3(RP2):c.769-19T>C rs782135264
NM_006915.3(RP2):c.769-20A>T rs906626842
NM_006915.3(RP2):c.810G>A (p.Val270=) rs1433246416
NM_006915.3(RP2):c.828T>G (p.Asp276Glu)
NM_006915.3(RP2):c.870T>A (p.Pro290=) rs1556319905
NM_006915.3(RP2):c.883+10G>A rs2519918723
NM_006915.3(RP2):c.883+20T>C
NM_006915.3(RP2):c.884-9T>G
NM_006915.3(RP2):c.903G>A (p.Glu301=)
NM_006915.3(RP2):c.912G>T (p.Gly304=) rs1925390675
NM_006915.3(RP2):c.963G>A (p.Gly321=) rs2519928548
NM_006915.3(RP2):c.969+18C>T
NM_006915.3(RP2):c.96C>T (p.Arg32=) rs2519902183
NM_006915.3(RP2):c.970-17_970-6del rs782713463
NM_006915.3(RP2):c.996G>T (p.Thr332=) rs781878258

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