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 0.01957
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.285C>G (p.Pro95=) rs374743004 0.00005
NM_006915.3(RP2):c.807A>G (p.Glu269=) rs148517937 0.00003
NM_006915.3(RP2):c.103-16T>A rs1346406616 0.00002
NM_006915.3(RP2):c.122T>C (p.Met41Thr) rs782356034 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.949G>A (p.Glu317Lys) rs782721235 0.00002
NM_006915.3(RP2):c.969+18C>G rs369210778 0.00002
NM_006915.3(RP2):c.167C>T (p.Thr56Met) rs1201646093 0.00001
NM_006915.3(RP2):c.750C>T (p.Ala250=) rs782562995 0.00001
NM_006915.3(RP2):c.768+13A>G rs1284693367 0.00001
NM_006915.3(RP2):c.102+13G>T
NM_006915.3(RP2):c.102+14T>A
NM_006915.3(RP2):c.102+17A>G
NM_006915.3(RP2):c.102+19C>A
NM_006915.3(RP2):c.102+20C>T
NM_006915.3(RP2):c.1026C>T (p.Asn342=)
NM_006915.3(RP2):c.1032T>C (p.Ala344=)
NM_006915.3(RP2):c.168G>A (p.Thr56=)
NM_006915.3(RP2):c.180A>G (p.Gln60=)
NM_006915.3(RP2):c.207C>T (p.Asn69=)
NM_006915.3(RP2):c.285C>T (p.Pro95=)
NM_006915.3(RP2):c.333A>G (p.Thr111=)
NM_006915.3(RP2):c.354T>C (p.Arg118=) rs1035661138
NM_006915.3(RP2):c.366T>C (p.Cys122=)
NM_006915.3(RP2):c.396C>G (p.Ala132=)
NM_006915.3(RP2):c.429C>A (p.Ile143=)
NM_006915.3(RP2):c.447A>G (p.Gln149=)
NM_006915.3(RP2):c.489G>A (p.Gly163=)
NM_006915.3(RP2):c.507T>C (p.Asn169=)
NM_006915.3(RP2):c.564T>C (p.Leu188=)
NM_006915.3(RP2):c.576T>C (p.Asp192=)
NM_006915.3(RP2):c.621C>G (p.Leu207=)
NM_006915.3(RP2):c.632G>A (p.Arg211His)
NM_006915.3(RP2):c.681G>A (p.Gln227=)
NM_006915.3(RP2):c.702A>G (p.Glu234=)
NM_006915.3(RP2):c.705A>G (p.Ser235=)
NM_006915.3(RP2):c.717A>G (p.Val239=)
NM_006915.3(RP2):c.720A>G (p.Leu240=)
NM_006915.3(RP2):c.768+12G>A
NM_006915.3(RP2):c.768+12G>C
NM_006915.3(RP2):c.769-19T>C
NM_006915.3(RP2):c.769-20A>T
NM_006915.3(RP2):c.810G>A (p.Val270=)
NM_006915.3(RP2):c.828T>G (p.Asp276Glu)
NM_006915.3(RP2):c.870T>A (p.Pro290=)
NM_006915.3(RP2):c.883+10G>A
NM_006915.3(RP2):c.883+19G>A
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>A (p.Gly304=)
NM_006915.3(RP2):c.912G>T (p.Gly304=)
NM_006915.3(RP2):c.948C>T (p.Asn316=)
NM_006915.3(RP2):c.963G>A (p.Gly321=)
NM_006915.3(RP2):c.969+18C>T
NM_006915.3(RP2):c.96C>G (p.Arg32=)
NM_006915.3(RP2):c.96C>T (p.Arg32=)
NM_006915.3(RP2):c.970-17_970-6del
NM_006915.3(RP2):c.970-9T>G
NM_006915.3(RP2):c.996G>T (p.Thr332=)

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