ClinVar Miner

List of variants in gene COL1A1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP
NM_000088.3(COL1A1):c.-43C>T rs368832341
NM_000088.3(COL1A1):c.1056+12dupC rs766175536
NM_000088.3(COL1A1):c.1233C>T (p.Phe411=) rs776387246
NM_000088.3(COL1A1):c.1249C>G (p.Pro417Ala) rs72648327
NM_000088.3(COL1A1):c.1269C>T (p.Pro423=) rs149301001
NM_000088.3(COL1A1):c.1300-9C>T rs780311548
NM_000088.3(COL1A1):c.1461+13G>T rs371161009
NM_000088.3(COL1A1):c.1515+20G>A rs373728987
NM_000088.3(COL1A1):c.1515+6C>T rs369422507
NM_000088.3(COL1A1):c.1533T>G (p.Arg511=) rs899423835
NM_000088.3(COL1A1):c.1587C>T (p.Pro529=) rs113437353
NM_000088.3(COL1A1):c.1615-4C>A rs41316657
NM_000088.3(COL1A1):c.1638C>T (p.Ser546=) rs146450504
NM_000088.3(COL1A1):c.165C>T (p.Pro55=) rs1057523677
NM_000088.3(COL1A1):c.1668+16C>T rs41316659
NM_000088.3(COL1A1):c.1768-18A>C rs767179998
NM_000088.3(COL1A1):c.1768-8C>T rs193922142
NM_000088.3(COL1A1):c.1785T>A (p.Ala595=) rs780217716
NM_000088.3(COL1A1):c.1812T>C (p.Pro604=) rs151328660
NM_000088.3(COL1A1):c.1815C>T (p.Gly605=) rs370384784
NM_000088.3(COL1A1):c.1822-32delA rs757681237
NM_000088.3(COL1A1):c.1873G>A (p.Ala625Thr) rs149561221
NM_000088.3(COL1A1):c.1875+8T>A rs756572885
NM_000088.3(COL1A1):c.1876-6G>A rs763222869
NM_000088.3(COL1A1):c.1887C>T (p.Gly629=) rs375695940
NM_000088.3(COL1A1):c.1929+17G>C rs1291997527
NM_000088.3(COL1A1):c.1930-5T>C rs762377921
NM_000088.3(COL1A1):c.1983+9G>C rs201091992
NM_000088.3(COL1A1):c.1983+9G>T rs201091992
NM_000088.3(COL1A1):c.1984-7C>G rs376886366
NM_000088.3(COL1A1):c.2115C>T (p.Asn705=) rs41316673
NM_000088.3(COL1A1):c.2127+12G>A rs778814970
NM_000088.3(COL1A1):c.2167G>A (p.Ala723Thr) rs150803124
NM_000088.3(COL1A1):c.2181G>A (p.Gln727=) rs777571745
NM_000088.3(COL1A1):c.2235+11C>A rs572426023
NM_000088.3(COL1A1):c.2235+11C>G rs572426023
NM_000088.3(COL1A1):c.2236-17C>G rs193922146
NM_000088.3(COL1A1):c.2343+18C>T rs1050837911
NM_000088.3(COL1A1):c.2344-7C>T rs1031284183
NM_000088.3(COL1A1):c.2397+13G>A rs200821764
NM_000088.3(COL1A1):c.2466A>G (p.Gln822=) rs551706871
NM_000088.3(COL1A1):c.2532C>T (p.Ala844=) rs374158703
NM_000088.3(COL1A1):c.2559T>A (p.Ile853=) rs764910205
NM_000088.3(COL1A1):c.2560-18C>T rs2075559
NM_000088.3(COL1A1):c.2595C>T (p.Arg865=) rs117672175
NM_000088.3(COL1A1):c.2613+13C>T rs368380161
NM_000088.3(COL1A1):c.2668-12A>G rs200355573
NM_000088.3(COL1A1):c.2668-7C>T rs1555572488
NM_000088.3(COL1A1):c.2716G>A (p.Gly906Ser) rs145446512
NM_000088.3(COL1A1):c.2829+20T>C rs372169804
NM_000088.3(COL1A1):c.2830-11G>A rs1555572425
NM_000088.3(COL1A1):c.2838T>G (p.Pro946=) rs1555572418
NM_000088.3(COL1A1):c.2932C>T (p.Pro978Ser) rs193922153
NM_000088.3(COL1A1):c.2937+9C>T rs1555572393
NM_000088.3(COL1A1):c.299-15C>T rs199523510
NM_000088.3(COL1A1):c.3045+3G>A rs41316695
NM_000088.3(COL1A1):c.3046-8_3046-5dup rs138425306
NM_000088.3(COL1A1):c.3099+15C>A rs1189154641
NM_000088.3(COL1A1):c.3102T>C (p.Gly1034=) rs147743501
NM_000088.3(COL1A1):c.3123C>T (p.Pro1041=) rs145608939
NM_000088.3(COL1A1):c.3237C>A (p.Gly1079=) rs374853330
NM_000088.3(COL1A1):c.3255C>T (p.Gly1085=) rs369670483
NM_000088.3(COL1A1):c.3309C>T (p.Gly1103=) rs142312753
NM_000088.3(COL1A1):c.3424-10C>T rs1555571948
NM_000088.3(COL1A1):c.3424-6C>A rs370865189
NM_000088.3(COL1A1):c.3465C>T (p.Leu1155=) rs368746726
NM_000088.3(COL1A1):c.3468C>T (p.Asn1156=) rs149980662
NM_000088.3(COL1A1):c.3504C>T (p.Arg1168=) rs370529603
NM_000088.3(COL1A1):c.3531+14C>T rs199766533
NM_000088.3(COL1A1):c.3532-13C>T rs369694934
NM_000088.3(COL1A1):c.3687C>T (p.Leu1229=) rs765353412
NM_000088.3(COL1A1):c.3726C>A (p.Ile1242=) rs768572265
NM_000088.3(COL1A1):c.3766G>A (p.Ala1256Thr) rs148216434
NM_000088.3(COL1A1):c.4017C>T (p.Gly1339=) rs201256042
NM_000088.3(COL1A1):c.4018G>A (p.Gly1340Ser) rs147936946
NM_000088.3(COL1A1):c.4080C>T (p.Thr1360=) rs753536372
NM_000088.3(COL1A1):c.408A>G (p.Gly136=) rs533127847
NM_000088.3(COL1A1):c.4181A>G (p.Asn1394Ser) rs147266928
NM_000088.3(COL1A1):c.4182C>T (p.Asn1394=) rs755763693
NM_000088.3(COL1A1):c.4362C>T (p.Phe1454=) rs758524007
NM_000088.3(COL1A1):c.459T>C (p.Pro153=) rs1555575026
NM_000088.3(COL1A1):c.471+14C>G rs774281966
NM_000088.3(COL1A1):c.544-4A>G rs369898579
NM_000088.3(COL1A1):c.588+15C>T rs371817394
NM_000088.3(COL1A1):c.589-20T>C rs370564344
NM_000088.3(COL1A1):c.627C>T (p.Gly209=) rs201136122
NM_000088.3(COL1A1):c.642+11T>C rs376087528
NM_000088.3(COL1A1):c.801C>T (p.His267=) rs769689009
NM_000088.3(COL1A1):c.904-9G>T rs141726413
NM_000088.3(COL1A1):c.999C>T (p.Pro333=) rs62637627

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