ClinVar Miner

List of variants in gene IGF1R reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_000875.5(IGF1R):c.*1087A>G rs2016873
NM_000875.5(IGF1R):c.*1152G>A
NM_000875.5(IGF1R):c.*1228G>A rs187193143
NM_000875.5(IGF1R):c.*1268del rs397772788
NM_000875.5(IGF1R):c.*1425A>C rs34237671
NM_000875.5(IGF1R):c.*1724C>T rs34718548
NM_000875.5(IGF1R):c.*1856C>T rs1058696
NM_000875.5(IGF1R):c.*2212G>A
NM_000875.5(IGF1R):c.*2426del rs398028512
NM_000875.5(IGF1R):c.*2529_*2530GT[6] rs398058004
NM_000875.5(IGF1R):c.*2856_*2857dup rs397836919
NM_000875.5(IGF1R):c.*2858_*2860del rs375554267
NM_000875.5(IGF1R):c.*3074G>A rs2002880
NM_000875.5(IGF1R):c.*3129G>T rs2016347
NM_000875.5(IGF1R):c.*3165T>C rs9282715
NM_000875.5(IGF1R):c.*3333G>A rs61736167
NM_000875.5(IGF1R):c.*3458G>A rs3743251
NM_000875.5(IGF1R):c.*3766C>T rs2684788
NM_000875.5(IGF1R):c.*4000C>T rs1815009
NM_000875.5(IGF1R):c.*4172C>T rs2654980
NM_000875.5(IGF1R):c.*417_*418del rs45484096
NM_000875.5(IGF1R):c.*4329G>A
NM_000875.5(IGF1R):c.*4391C>T rs2684787
NM_000875.5(IGF1R):c.*4458C>G rs2654981
NM_000875.5(IGF1R):c.*4512G>A
NM_000875.5(IGF1R):c.*4513A>G rs542634107
NM_000875.5(IGF1R):c.*4645C>T rs3743250
NM_000875.5(IGF1R):c.*4752G>T rs3743249
NM_000875.5(IGF1R):c.*4814C>T rs2684786
NM_000875.5(IGF1R):c.*4815G>A rs145781849
NM_000875.5(IGF1R):c.*5146G>A rs78982292
NM_000875.5(IGF1R):c.*5151T>C rs28393861
NM_000875.5(IGF1R):c.*5157A>G
NM_000875.5(IGF1R):c.*5227C>T rs182645795
NM_000875.5(IGF1R):c.*5309C>T rs2684785
NM_000875.5(IGF1R):c.*5436C>T rs111563582
NM_000875.5(IGF1R):c.*5458A>G rs117503139
NM_000875.5(IGF1R):c.*5528G>A
NM_000875.5(IGF1R):c.*5570C>T rs116922843
NM_000875.5(IGF1R):c.*6069G>A
NM_000875.5(IGF1R):c.*6092G>A rs74534003
NM_000875.5(IGF1R):c.*6166G>A rs111990961
NM_000875.5(IGF1R):c.*6186G>A rs73465768
NM_000875.5(IGF1R):c.*6271C>T rs2177031
NM_000875.5(IGF1R):c.*6493C>T rs142100490
NM_000875.5(IGF1R):c.*6568A>C rs144178122
NM_000875.5(IGF1R):c.*874C>T rs34875596
NM_000875.5(IGF1R):c.*977C>T
NM_000875.5(IGF1R):c.1336A>G (p.Met446Val) rs117440569
NM_000875.5(IGF1R):c.1686G>A (p.Val562=) rs2228531
NM_000875.5(IGF1R):c.1914C>T (p.Asn638=) rs45506098
NM_000875.5(IGF1R):c.2298C>T (p.Thr766=) rs3743262
NM_000875.5(IGF1R):c.2570A>G (p.Asn857Ser) rs45611935
NM_000875.5(IGF1R):c.3129G>A (p.Glu1043=) rs2229765
NM_000875.5(IGF1R):c.3298-9C>G rs7168369
NM_000875.5(IGF1R):c.402G>A (p.Arg134=) rs35385418
NM_000875.5(IGF1R):c.4038C>T (p.Tyr1346=) rs17847203
NM_000875.5(IGF1R):c.846C>T (p.Cys282=) rs35171849
NM_000875.5(IGF1R):c.864C>T (p.Ala288=) rs34430460
NM_000875.5(IGF1R):c.885G>A (p.Gly295=) rs56303650
NM_000875.5(IGF1R):c.903C>A (p.Gly301=) rs2229764

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