ClinVar Miner

List of variants in gene RIMS1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_014989.5(RIMS1):c.*1390dup rs142802827
NM_014989.5(RIMS1):c.-182_-180dup rs555947867
NM_014989.5(RIMS1):c.1384C>A (p.Pro462Thr) rs541997223
NM_014989.5(RIMS1):c.169G>C (p.Val57Leu) rs200005095
NM_014989.5(RIMS1):c.1758G>A (p.Thr586=)
NM_014989.5(RIMS1):c.2294A>G (p.Gln765Arg) rs199629596
NM_014989.5(RIMS1):c.2523A>G (p.Glu841=) rs186078277
NM_014989.5(RIMS1):c.2894C>T (p.Pro965Leu) rs752875047
NM_014989.5(RIMS1):c.3399-4A>G rs368216570
NM_014989.5(RIMS1):c.3430C>T (p.Arg1144Ter)
NM_014989.5(RIMS1):c.3703G>A (p.Gly1235Arg)
NM_014989.5(RIMS1):c.3758C>T (p.Pro1253Leu)
NM_014989.5(RIMS1):c.3921G>T (p.Gly1307=) rs769179703
NM_014989.5(RIMS1):c.39C>G (p.Pro13=)
NM_014989.5(RIMS1):c.4159C>T (p.Arg1387Trp) rs201017334
NM_014989.5(RIMS1):c.4191G>A (p.Lys1397=) rs372513852
NM_014989.5(RIMS1):c.4197C>T (p.Thr1399=) rs201885523
NM_014989.5(RIMS1):c.423G>A (p.Ala141=)
NM_014989.5(RIMS1):c.4599C>T (p.Thr1533=)
NM_014989.5(RIMS1):c.4945T>A (p.Ser1649Thr)
NM_014989.5(RIMS1):c.798A>G (p.Glu266=) rs755868505
NM_014989.5(RIMS1):c.826G>A (p.Gly276Arg)
NM_014989.5(RIMS1):c.928C>T (p.Arg310Cys)

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