ClinVar Miner

List of variants in gene NOTCH1 reported as likely benign for not provided

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Gene type:
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Total variants: 63
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HGVS dbSNP
NM_017617.5(NOTCH1):c.-6G>T
NM_017617.5(NOTCH1):c.1041C>T (p.Gly347=)
NM_017617.5(NOTCH1):c.1100-141C>G
NM_017617.5(NOTCH1):c.1255+15_1255+16del
NM_017617.5(NOTCH1):c.140+257A>T
NM_017617.5(NOTCH1):c.140+71G>A
NM_017617.5(NOTCH1):c.1407C>T (p.Asp469=)
NM_017617.5(NOTCH1):c.147C>T (p.Gly49=) rs746002433
NM_017617.5(NOTCH1):c.1512C>A (p.Arg504=)
NM_017617.5(NOTCH1):c.1555+60G>T
NM_017617.5(NOTCH1):c.1650C>T (p.Tyr550=) rs371634784
NM_017617.5(NOTCH1):c.1669+16C>T
NM_017617.5(NOTCH1):c.1699A>G (p.Ile567Val) rs369067940
NM_017617.5(NOTCH1):c.1731C>T (p.Tyr577=)
NM_017617.5(NOTCH1):c.1869C>T (p.Asn623=)
NM_017617.5(NOTCH1):c.1956G>T (p.Ser652=)
NM_017617.5(NOTCH1):c.2112C>T (p.Cys704=) rs757495549
NM_017617.5(NOTCH1):c.2452C>T (p.Leu818=)
NM_017617.5(NOTCH1):c.2467+177G>A
NM_017617.5(NOTCH1):c.2467+28A>G
NM_017617.5(NOTCH1):c.2468-197C>T
NM_017617.5(NOTCH1):c.2468-287G>A
NM_017617.5(NOTCH1):c.2588-93C>T
NM_017617.5(NOTCH1):c.263G>A (p.Ser88Asn) rs191357265
NM_017617.5(NOTCH1):c.2740+128G>A
NM_017617.5(NOTCH1):c.2740+187C>T
NM_017617.5(NOTCH1):c.2740+188G>A
NM_017617.5(NOTCH1):c.2740+295C>T
NM_017617.5(NOTCH1):c.2772C>T (p.Asp924=)
NM_017617.5(NOTCH1):c.2969+182C>T
NM_017617.5(NOTCH1):c.2969+308C>T
NM_017617.5(NOTCH1):c.3042G>A (p.Thr1014=) rs371532644
NM_017617.5(NOTCH1):c.3171+153G>A
NM_017617.5(NOTCH1):c.3171+8C>T
NM_017617.5(NOTCH1):c.3510+148G>A
NM_017617.5(NOTCH1):c.3511-175G>A
NM_017617.5(NOTCH1):c.3684C>T (p.Pro1228=)
NM_017617.5(NOTCH1):c.3852C>T (p.Cys1284=) rs377289044
NM_017617.5(NOTCH1):c.404-117T>C
NM_017617.5(NOTCH1):c.411G>T (p.Ser137=)
NM_017617.5(NOTCH1):c.4710G>A (p.Ala1570=) rs773978978
NM_017617.5(NOTCH1):c.4719G>A (p.Thr1573=) rs775105774
NM_017617.5(NOTCH1):c.5019-286G>A
NM_017617.5(NOTCH1):c.5019-51C>T
NM_017617.5(NOTCH1):c.5103A>G (p.Ala1701=) rs776610176
NM_017617.5(NOTCH1):c.5168-7C>T
NM_017617.5(NOTCH1):c.516C>T (p.Gly172=)
NM_017617.5(NOTCH1):c.558C>T (p.Pro186=) rs756111268
NM_017617.5(NOTCH1):c.5715C>T (p.Asp1905=) rs748200129
NM_017617.5(NOTCH1):c.5913C>T (p.Ala1971=)
NM_017617.5(NOTCH1):c.608G>A (p.Arg203His) rs182763411
NM_017617.5(NOTCH1):c.6180+126G>A
NM_017617.5(NOTCH1):c.6223G>A (p.Glu2075Lys)
NM_017617.5(NOTCH1):c.6570G>A (p.Leu2190=)
NM_017617.5(NOTCH1):c.6570G>C (p.Leu2190=) rs200630233
NM_017617.5(NOTCH1):c.6607C>T (p.Leu2203=)
NM_017617.5(NOTCH1):c.6666G>A (p.Pro2222=) rs202229687
NM_017617.5(NOTCH1):c.6739C>T (p.Leu2247=)
NM_017617.5(NOTCH1):c.6744C>T (p.Asn2248=) rs372771288
NM_017617.5(NOTCH1):c.6789G>C (p.Arg2263=)
NM_017617.5(NOTCH1):c.6966A>G (p.Gln2322=)
NM_017617.5(NOTCH1):c.865+240A>G
NM_017617.5(NOTCH1):c.865+251G>A

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