ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000875.4(IGF1R):c.*1087A>G rs2016873
NM_000875.4(IGF1R):c.*1425A>C rs34237671
NM_000875.4(IGF1R):c.*15A>G rs45561434
NM_000875.4(IGF1R):c.*1724C>T rs34718548
NM_000875.4(IGF1R):c.*1763_*1764dupAT rs760831806
NM_000875.4(IGF1R):c.*1856C>T rs1058696
NM_000875.4(IGF1R):c.*3020dupT rs397824885
NM_000875.4(IGF1R):c.*3074G>A rs2002880
NM_000875.4(IGF1R):c.*3333G>A rs61736167
NM_000875.4(IGF1R):c.*3471dupC rs3833014
NM_000875.4(IGF1R):c.*4172C>T rs2654980
NM_000875.4(IGF1R):c.*4391C>T rs2684787
NM_000875.4(IGF1R):c.*4814C>T rs2684786
NM_000875.4(IGF1R):c.*5146G>A rs78982292
NM_000875.4(IGF1R):c.*5309C>T rs2684785
NM_000875.4(IGF1R):c.*5436C>T rs111563582
NM_000875.4(IGF1R):c.*5458A>G rs117503139
NM_000875.4(IGF1R):c.*5736_*5739delTTTT rs112539877
NM_000875.4(IGF1R):c.*6092G>A rs74534003
NM_000875.4(IGF1R):c.*6166G>A rs111990961
NM_000875.4(IGF1R):c.*6186G>A rs73465768
NM_000875.4(IGF1R):c.*626T>C rs34804698
NM_000875.4(IGF1R):c.*6580C>T rs78536914
NM_000875.4(IGF1R):c.*7046_*7050dupAAGTA rs373668848
NM_000875.4(IGF1R):c.*874C>T rs34875596
NM_000875.4(IGF1R):c.*910C>T rs702497
NM_000875.4(IGF1R):c.1463-5C>A rs36108138
NM_000875.4(IGF1R):c.2700C>T (p.Asn900=) rs56400113
NM_000875.4(IGF1R):c.4038C>T (p.Tyr1346=) rs17847203
NM_000875.4(IGF1R):c.864C>T (p.Ala288=) rs34430460
NM_000875.4(IGF1R):c.885G>A (p.Gly295=) rs56303650
NM_000875.4(IGF1R):c.903C>A (p.Gly301=) rs2229764

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