ClinVar Miner

List of variants in gene INS, INS-IGF2 studied for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_000207.3(INS):c.188-16C>T rs5507 0.00616
NM_000207.3(INS):c.63A>G (p.Pro21=) rs11564720 0.00546
NM_000207.3(INS):c.188-10G>A rs41275198 0.00262
NM_000207.3(INS):c.227G>A (p.Ser76Asn) rs139264769 0.00050
NM_000207.3(INS):c.17G>A (p.Arg6His) rs121908259 0.00019
NM_000207.3(INS):c.*28G>A rs778107057 0.00010
NM_000207.3(INS):c.*2C>T rs200306755 0.00006
NM_000207.3(INS):c.*42C>T rs376867722 0.00006
NM_000207.3(INS):c.130G>A (p.Gly44Arg) rs765512575 0.00003
NM_000207.3(INS):c.16C>T (p.Arg6Cys) rs121908278 0.00003
NM_000207.3(INS):c.66C>T (p.Ala22=) rs375371953 0.00003
NM_000207.3(INS):c.202C>A (p.Leu68Met) rs121908279 0.00002
NM_000207.3(INS):c.1A>G (p.Met1Val) rs757124361 0.00001
NM_000207.3(INS):c.25C>T (p.Pro9Ser) rs372122432 0.00001
NM_000207.2(INS):c.(?_-191)_(187_?)+1del
NM_000207.3(INS):c.*59A>G rs397515519
NM_000207.3(INS):c.-18+3C>G rs886048112
NM_000207.3(INS):c.-39A>C rs1554921033
NM_000207.3(INS):c.101A>C (p.His34Pro) rs1564912274
NM_000207.3(INS):c.103C>A (p.Leu35Met) rs1278232284
NM_000207.3(INS):c.104T>A (p.Leu35Gln)
NM_000207.3(INS):c.104T>C (p.Leu35Pro) rs121908273
NM_000207.3(INS):c.115C>T (p.Leu39Phe) rs2133676660
NM_000207.3(INS):c.125T>C (p.Val42Ala) rs886037863
NM_000207.3(INS):c.127T>G (p.Cys43Gly) rs80356666
NM_000207.3(INS):c.137G>A (p.Arg46Gln) rs121908260
NM_000207.3(INS):c.140G>T (p.Gly47Val) rs80356667
NM_000207.3(INS):c.143T>G (p.Phe48Cys) rs80356668
NM_000207.3(INS):c.153A>G (p.Thr51=) rs773789432
NM_000207.3(INS):c.155C>A (p.Pro52His) rs145038693
NM_000207.3(INS):c.155C>T (p.Pro52Leu) rs145038693
NM_000207.3(INS):c.163C>T (p.Arg55Cys) rs121908261
NM_000207.3(INS):c.174del (p.Glu59fs) rs1845873878
NM_000207.3(INS):c.187+15C>A rs754089310
NM_000207.3(INS):c.187+241G>A rs886041083
NM_000207.3(INS):c.188-31G>A rs797045623
NM_000207.3(INS):c.188-3C>A rs886048111
NM_000207.3(INS):c.250G>A (p.Gly84Arg) rs121908274
NM_000207.3(INS):c.265C>T (p.Arg89Cys) rs80356669
NM_000207.3(INS):c.268G>T (p.Gly90Cys) rs80356670
NM_000207.3(INS):c.26C>G (p.Pro9Arg) rs1564912403
NM_000207.3(INS):c.274G>T (p.Val92Leu) rs121918102
NM_000207.3(INS):c.278A>G (p.Glu93Gly) rs1057524907
NM_000207.3(INS):c.286T>C (p.Cys96Arg) rs1845839718
NM_000207.3(INS):c.287G>A (p.Cys96Tyr) rs80356671
NM_000207.3(INS):c.287G>C (p.Cys96Ser) rs80356671
NM_000207.3(INS):c.290C>G (p.Thr97Ser) rs1564911425
NM_000207.3(INS):c.293G>T (p.Ser98Ile) rs2133672883
NM_000207.3(INS):c.302C>G (p.Ser101Cys) rs121908276
NM_000207.3(INS):c.308A>G (p.Tyr103Cys) rs121908277
NM_000207.3(INS):c.322T>G (p.Tyr108Asp) rs2133672778
NM_000207.3(INS):c.323A>G (p.Tyr108Cys) rs80356672
NM_000207.3(INS):c.326G>T (p.Cys109Phe) rs2133672742
NM_000207.3(INS):c.3G>A (p.Met1Ile) rs397515521
NM_000207.3(INS):c.3G>T (p.Met1Ile) rs397515521
NM_000207.3(INS):c.67G>A (p.Ala23Thr) rs13306444
NM_000207.3(INS):c.71C>A (p.Ala24Asp) rs80356663
NM_000207.3(INS):c.71C>T (p.Ala24Val) rs80356663
NM_000207.3(INS):c.72C>A (p.Ala24=) rs539284976
NM_000207.3(INS):c.85C>G (p.His29Asp) rs121908272
NM_000207.3(INS):c.94G>A (p.Gly32Ser) rs80356664
NM_000207.3(INS):c.94G>C (p.Gly32Arg) rs80356664

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