ClinVar Miner

List of variants in gene INSR reported as likely benign for Pineal hyperplasia AND diabetes mellitus syndrome

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
NM_000208.3(INSR):c.*4803G>A rs138569451
NM_000208.4(INSR):c.*1089A>G rs116422284
NM_000208.4(INSR):c.*1116G>A rs146905190
NM_000208.4(INSR):c.*1171C>T rs188386673
NM_000208.4(INSR):c.*1191T>C rs564677377
NM_000208.4(INSR):c.*1192G>A rs142596192
NM_000208.4(INSR):c.*12G>A rs375751275
NM_000208.4(INSR):c.*1432C>T rs111557734
NM_000208.4(INSR):c.*1799C>T rs147080388
NM_000208.4(INSR):c.*1870C>G rs41315072
NM_000208.4(INSR):c.*2014C>T rs556567528
NM_000208.4(INSR):c.*2160G>T rs570523460
NM_000208.4(INSR):c.*224C>T rs2860171
NM_000208.4(INSR):c.*2255T>G rs547131375
NM_000208.4(INSR):c.*2318G>A rs80330850
NM_000208.4(INSR):c.*2340A>G rs78987925
NM_000208.4(INSR):c.*2456C>T rs145777450
NM_000208.4(INSR):c.*2464C>T rs181555180
NM_000208.4(INSR):c.*2502A>G rs149795309
NM_000208.4(INSR):c.*2519G>A rs114982195
NM_000208.4(INSR):c.*2565C>T rs117532686
NM_000208.4(INSR):c.*2820G>A rs139376149
NM_000208.4(INSR):c.*3029T>C rs72988602
NM_000208.4(INSR):c.*3298C>T rs184243377
NM_000208.4(INSR):c.*3359G>A rs146249924
NM_000208.4(INSR):c.*3365C>A rs561270909
NM_000208.4(INSR):c.*3463A>G rs115358150
NM_000208.4(INSR):c.*3541C>T rs116953519
NM_000208.4(INSR):c.*3685T>C rs143409422
NM_000208.4(INSR):c.*3877T>C rs148660410
NM_000208.4(INSR):c.*3894G>A rs184154294
NM_000208.4(INSR):c.*394del rs140291876
NM_000208.4(INSR):c.*4602C>T rs10413914
NM_000208.4(INSR):c.*4760G>A rs574836227
NM_000208.4(INSR):c.*498_*499insTT rs71775166
NM_000208.4(INSR):c.*501T>G rs562228680
NM_000208.4(INSR):c.-12G>C rs143135433
NM_000208.4(INSR):c.1080C>T (p.Cys360=) rs56066516
NM_000208.4(INSR):c.1098T>C (p.Ser366=) rs2229435
NM_000208.4(INSR):c.1123+13G>T rs72549236
NM_000208.4(INSR):c.190T>C (p.Leu64=) rs144836032
NM_000208.4(INSR):c.2193G>A (p.Thr731=) rs6413501
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu) rs143523271
NM_000208.4(INSR):c.2245G>A (p.Gly749Ser) rs545885277
NM_000208.4(INSR):c.2280A>G (p.Lys760=) rs373695282
NM_000208.4(INSR):c.2295C>T (p.Gly765=) rs142654992
NM_000208.4(INSR):c.2370G>A (p.Thr790=) rs16994210
NM_000208.4(INSR):c.2448G>A (p.Thr816=) rs2229434
NM_000208.4(INSR):c.2526G>C (p.Ala842=) rs2229430
NM_000208.4(INSR):c.2542+3A>G rs13306451
NM_000208.4(INSR):c.2572A>G (p.Thr858Ala) rs182552223
NM_000208.4(INSR):c.262T>C (p.Leu88=) rs61736580
NM_000208.4(INSR):c.2643C>T (p.Ile881=) rs2229432
NM_000208.4(INSR):c.2682+9C>G rs41398545
NM_000208.4(INSR):c.2718T>C (p.Ala906=) rs2229433
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu) rs146588336
NM_000208.4(INSR):c.2853G>A (p.Pro951=) rs200564313
NM_000208.4(INSR):c.2946-14T>C rs138585749
NM_000208.4(INSR):c.3193C>G (p.Leu1065Val) rs56395521
NM_000208.4(INSR):c.3370-12T>G rs200201955
NM_000208.4(INSR):c.3370-15G>A rs41300628
NM_000208.4(INSR):c.3383G>A (p.Arg1128His) rs202160383
NM_000208.4(INSR):c.39G>C (p.Pro13=) rs771984795
NM_000208.4(INSR):c.4082A>G (p.Tyr1361Cys) rs13306449
NM_000208.4(INSR):c.618C>T (p.Val206=) rs56012021
NM_000208.4(INSR):c.687C>T (p.Thr229=) rs150568177
NM_000208.4(INSR):c.909G>A (p.Gln303=) rs9282757

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