ClinVar Miner

List of variants in gene ARCN1 reported as benign for not provided

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001655.5(ARCN1):c.985-203T>A rs2276079 0.17665
NM_001655.5(ARCN1):c.1530T>C (p.Ile510=) rs11216925 0.15677
NM_001655.5(ARCN1):c.447+104A>G rs17842763 0.15647
NM_001655.5(ARCN1):c.268-213A>G rs11216913 0.15493
NM_001655.5(ARCN1):c.268-6G>A rs78730658 0.00569
NM_001655.5(ARCN1):c.786C>G (p.Thr262=) rs141830134 0.00242
NM_001655.5(ARCN1):c.984+3G>A rs148276430 0.00181
NM_001655.5(ARCN1):c.935G>A (p.Arg312Gln) rs138250193 0.00081
NM_001655.5(ARCN1):c.16G>T (p.Ala6Ser) rs138863361 0.00057
NM_001655.5(ARCN1):c.1467A>G (p.Val489=) rs144108474 0.00056
NM_001655.5(ARCN1):c.867C>T (p.Asp289=) rs371011063 0.00010
NM_001655.5(ARCN1):c.1257G>A (p.Ala419=) rs782706299 0.00004
NM_001655.5(ARCN1):c.438C>T (p.Ala146=) rs556971767 0.00004
NM_001655.5(ARCN1):c.1242-132_1242-131insAGAG rs10674058
NM_001655.5(ARCN1):c.1266C>T (p.Ile422=)
NM_001655.5(ARCN1):c.163A>C (p.Arg55=)
NM_001655.5(ARCN1):c.267+110G>C rs11216912
NM_001655.5(ARCN1):c.268-3T>C
NM_001655.5(ARCN1):c.268-7C>T
NM_001655.5(ARCN1):c.4-60T>C rs11216911
NM_001655.5(ARCN1):c.752C>T (p.Ser251Phe)
NM_001655.5(ARCN1):c.767A>G (p.Lys256Arg)

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