ClinVar Miner

List of variants in gene SMC1A reported as likely benign

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Gene type:
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Total variants: 105
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HGVS dbSNP
NM_001281463.1(SMC1A):c.*14C>T rs112727682
NM_001281463.1(SMC1A):c.*2540C>G rs182535846
NM_001281463.1(SMC1A):c.*2589A>G rs782291666
NM_001281463.1(SMC1A):c.*2973C>T rs56110615
NM_001281463.1(SMC1A):c.*3838G>A rs144702614
NM_001281463.1(SMC1A):c.*4645T>C rs150365487
NM_001281463.1(SMC1A):c.*4952_*4953del rs782700101
NM_001281463.1(SMC1A):c.*5380G>A rs186354950
NM_001281463.1(SMC1A):c.*96C>T rs139317060
NM_001281463.1(SMC1A):c.-150C>T rs781999328
NM_001281463.1(SMC1A):c.1032G>A (p.Thr344=) rs140585416
NM_001281463.1(SMC1A):c.1257C>T (p.Tyr419=) rs144850468
NM_001281463.1(SMC1A):c.1482C>T (p.Tyr494=) rs782547781
NM_001281463.1(SMC1A):c.1692G>T (p.Arg564=) rs782379340
NM_001281463.1(SMC1A):c.2125C>T (p.Leu709=) rs782301753
NM_001281463.1(SMC1A):c.2131-5T>C rs2297104
NM_001281463.1(SMC1A):c.219C>G (p.Ala73=) rs587784414
NM_001281463.1(SMC1A):c.232+12T>C rs782781148
NM_001281463.1(SMC1A):c.2390T>G (p.Ile797Ser) rs587784413
NM_001281463.1(SMC1A):c.2580G>A (p.Ser860=) rs1193658492
NM_001281463.1(SMC1A):c.2722C>T (p.Leu908=) rs781912370
NM_001281463.1(SMC1A):c.2758C>T (p.Leu920=) rs139654605
NM_001281463.1(SMC1A):c.2884G>A (p.Gly962Ser) rs782381563
NM_001281463.1(SMC1A):c.3324C>T (p.Gly1108=) rs374246357
NM_001281463.1(SMC1A):c.3384C>T (p.Ala1128=) rs142611198
NM_001281463.1(SMC1A):c.3525C>T (p.Ala1175=) rs146216425
NM_001281463.1(SMC1A):c.3552+7C>T rs782267492
NM_001281463.1(SMC1A):c.3597C>T (p.Thr1199=) rs28997583
NM_001281463.1(SMC1A):c.414T>A (p.Arg138=) rs782369322
NM_001281463.1(SMC1A):c.550-6G>A rs587784424
NM_001281463.1(SMC1A):c.768G>A (p.Gln256=) rs1569358988
NM_006306.4(SMC1A):c.*3087G>A
NM_006306.4(SMC1A):c.1023G>A (p.Leu341=)
NM_006306.4(SMC1A):c.1101G>A (p.Leu367=) rs782695048
NM_006306.4(SMC1A):c.1158A>G (p.Ala386=)
NM_006306.4(SMC1A):c.1254+8A>G
NM_006306.4(SMC1A):c.1290G>A (p.Glu430=)
NM_006306.4(SMC1A):c.1338-4G>A
NM_006306.4(SMC1A):c.1431G>C (p.Leu477=)
NM_006306.4(SMC1A):c.1563C>T (p.Asp521=)
NM_006306.4(SMC1A):c.1578A>G (p.Thr526=)
NM_006306.4(SMC1A):c.1647G>C (p.Ser549=)
NM_006306.4(SMC1A):c.1726C>T (p.Leu576=)
NM_006306.4(SMC1A):c.1860C>T (p.Asp620=)
NM_006306.4(SMC1A):c.1863C>T (p.Asn621=) rs782665597
NM_006306.4(SMC1A):c.1912-4G>T
NM_006306.4(SMC1A):c.192G>C (p.Leu64=)
NM_006306.4(SMC1A):c.1933C>T (p.Leu645=)
NM_006306.4(SMC1A):c.1938C>T (p.Phe646=)
NM_006306.4(SMC1A):c.2039G>A (p.Arg680His) rs1556889522
NM_006306.4(SMC1A):c.2059-9T>C rs782041729
NM_006306.4(SMC1A):c.2157A>G (p.Leu719=)
NM_006306.4(SMC1A):c.2184C>A (p.Ala728=) rs968499171
NM_006306.4(SMC1A):c.2205C>A (p.Ser735=)
NM_006306.4(SMC1A):c.2421-4A>G
NM_006306.4(SMC1A):c.2461T>C (p.Leu821=)
NM_006306.4(SMC1A):c.2505A>G (p.Val835=)
NM_006306.4(SMC1A):c.2556C>A (p.Leu852=) rs1602407405
NM_006306.4(SMC1A):c.2583G>A (p.Lys861=) rs1602405816
NM_006306.4(SMC1A):c.2598C>A (p.Thr866=)
NM_006306.4(SMC1A):c.2643G>A (p.Lys881=) rs1602405773
NM_006306.4(SMC1A):c.2688G>A (p.Lys896=) rs1602405737
NM_006306.4(SMC1A):c.2694C>T (p.Leu898=)
NM_006306.4(SMC1A):c.27T>C (p.Ile9=)
NM_006306.4(SMC1A):c.2838C>T (p.Thr946=)
NM_006306.4(SMC1A):c.2863-8C>T rs782738954
NM_006306.4(SMC1A):c.2886A>C (p.Ser962=) rs782788248
NM_006306.4(SMC1A):c.2949C>T (p.Tyr983=) rs1390804289
NM_006306.4(SMC1A):c.2979C>T (p.Ala993=)
NM_006306.4(SMC1A):c.298+9G>A rs1556891082
NM_006306.4(SMC1A):c.3003A>G (p.Gln1001=)
NM_006306.4(SMC1A):c.3063C>T (p.Ala1021=) rs202083908
NM_006306.4(SMC1A):c.3135T>C (p.Phe1045=) rs1602398671
NM_006306.4(SMC1A):c.3174A>G (p.Ala1058=)
NM_006306.4(SMC1A):c.3177C>T (p.Phe1059=) rs375312256
NM_006306.4(SMC1A):c.3205C>T (p.Arg1069Cys)
NM_006306.4(SMC1A):c.3267C>G (p.Ser1089=)
NM_006306.4(SMC1A):c.3286-4C>T rs1556885985
NM_006306.4(SMC1A):c.3437+10A>T rs782079503
NM_006306.4(SMC1A):c.3463C>T (p.Leu1155=)
NM_006306.4(SMC1A):c.3555C>T (p.Ile1185=)
NM_006306.4(SMC1A):c.3591C>G (p.Ala1197=)
NM_006306.4(SMC1A):c.3615T>A (p.Pro1205=) rs1602397790
NM_006306.4(SMC1A):c.3618+8G>A
NM_006306.4(SMC1A):c.3651C>T (p.Thr1217=)
NM_006306.4(SMC1A):c.3660C>T (p.Leu1220=)
NM_006306.4(SMC1A):c.3663C>G (p.Thr1221=)
NM_006306.4(SMC1A):c.3666G>A (p.Lys1222=) rs1602397606
NM_006306.4(SMC1A):c.372G>C (p.Leu124Phe) rs148835205
NM_006306.4(SMC1A):c.381C>T (p.Leu127=)
NM_006306.4(SMC1A):c.402C>T (p.Leu134=)
NM_006306.4(SMC1A):c.429T>C (p.Ile143=)
NM_006306.4(SMC1A):c.453G>A (p.Arg151=)
NM_006306.4(SMC1A):c.462A>G (p.Leu154=)
NM_006306.4(SMC1A):c.495G>A (p.Ala165=)
NM_006306.4(SMC1A):c.552T>C (p.Phe184=) rs1556890821
NM_006306.4(SMC1A):c.579G>A (p.Ala193=) rs199571320
NM_006306.4(SMC1A):c.594A>G (p.Glu198=) rs1556890814
NM_006306.4(SMC1A):c.616-7del rs1312306004
NM_006306.4(SMC1A):c.669G>C (p.Leu223=)
NM_006306.4(SMC1A):c.675C>T (p.Leu225=)
NM_006306.4(SMC1A):c.764G>A (p.Arg255His)
NM_006306.4(SMC1A):c.846G>A (p.Lys282=) rs1602413372
NM_006306.4(SMC1A):c.915C>T (p.Thr305=) rs782522248
NM_006306.4(SMC1A):c.951G>A (p.Lys317=)

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