ClinVar Miner

List of variants in gene RIMS1 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_014989.7(RIMS1):c.1083A>G (p.Leu361=) rs2463730 0.97497
NM_014989.7(RIMS1):c.666A>G (p.Leu222=) rs2249021 0.68629
NM_014989.7(RIMS1):c.1209G>A (p.Ala403=) rs114505309 0.27986
NM_014989.7(RIMS1):c.4548C>T (p.Phe1516=) rs2815738 0.20033
NM_014989.7(RIMS1):c.3470C>T (p.Pro1157Leu) rs41265501 0.02304
NM_014989.7(RIMS1):c.1776G>A (p.Glu592=) rs77121218 0.01826
NM_014989.7(RIMS1):c.743C>T (p.Ser248Leu) rs116476753 0.01524
NM_014989.7(RIMS1):c.648G>A (p.Ser216=) rs116303981 0.00829
NM_014989.7(RIMS1):c.2895G>A (p.Pro965=) rs41265493 0.00819
NM_014989.7(RIMS1):c.3923C>A (p.Ser1308Tyr) rs375771440 0.00042
NM_014989.7(RIMS1):c.3117-7G>A rs202107254 0.00032
NM_014989.7(RIMS1):c.3194+9C>A rs564292772 0.00017
NM_014989.7(RIMS1):c.4197C>T (p.Thr1399=) rs201885523 0.00016
NM_014989.7(RIMS1):c.798A>G (p.Glu266=) rs755868505 0.00016
NM_014989.7(RIMS1):c.1533G>A (p.Pro511=) rs201473375 0.00006
NM_014989.7(RIMS1):c.4506-5G>A rs201556693 0.00006
NM_014989.7(RIMS1):c.4317T>C (p.Val1439=) rs372862808 0.00003
NM_014989.7(RIMS1):c.2241T>C (p.Ser747=) rs760492397 0.00001
NM_014989.7(RIMS1):c.3738-20G>A rs771118720 0.00001
NM_014989.7(RIMS1):c.1034A>G (p.Gln345Arg)
NM_014989.7(RIMS1):c.1679-16593G>A
NM_014989.7(RIMS1):c.1679-20579A>G
NM_014989.7(RIMS1):c.1679-20587G>A rs181193740
NM_014989.7(RIMS1):c.2771-2A>G
NM_014989.7(RIMS1):c.3959C>T (p.Ser1320Phe) rs140943787
NM_014989.7(RIMS1):c.471+70C>T
NM_014989.7(RIMS1):c.876C>G (p.Arg292=) rs776775023

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