ClinVar Miner

List of variants in gene IGF1R reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_000875.5(IGF1R):c.*4000C>T rs1815009 0.65160
NM_000875.5(IGF1R):c.*3766C>T rs2684788 0.51536
NM_000875.5(IGF1R):c.1590-20T>C rs2272037 0.49319
NM_000875.5(IGF1R):c.3129G>A (p.Glu1043=) rs2229765 0.39376
NM_000875.5(IGF1R):c.640+20C>T rs7174918 0.25307
NM_000875.5(IGF1R):c.4038C>T (p.Tyr1346=) rs17847203 0.06905
NM_000875.5(IGF1R):c.2298C>T (p.Thr766=) rs3743262 0.05461
NM_000875.5(IGF1R):c.864C>T (p.Ala288=) rs34430460 0.02169
NM_000875.5(IGF1R):c.903C>A (p.Gly301=) rs2229764 0.01591
NM_000875.5(IGF1R):c.1463-5C>A rs36108138 0.01246
NM_000875.5(IGF1R):c.*1885G>C rs34530803 0.00976
NM_000875.5(IGF1R):c.1686G>A (p.Val562=) rs2228531 0.00884
NM_000875.5(IGF1R):c.1914C>T (p.Asn638=) rs45506098 0.00771
NM_000875.5(IGF1R):c.2700C>T (p.Asn900=) rs56400113 0.00749
NM_000875.5(IGF1R):c.402G>A (p.Arg134=) rs35385418 0.00679
NM_000875.5(IGF1R):c.3298-9C>G rs7168369 0.00488
NM_000875.5(IGF1R):c.1950G>T (p.Arg650=) rs56294552 0.00378
NM_000875.5(IGF1R):c.846C>T (p.Cys282=) rs35171849 0.00328
NM_000875.5(IGF1R):c.225C>T (p.Phe75=) rs55770488 0.00312
NM_000875.5(IGF1R):c.1310G>A (p.Arg437His) rs34516635 0.00287
NM_000875.5(IGF1R):c.2782+17G>A rs186895929 0.00244
NM_000875.5(IGF1R):c.1474G>A (p.Val492Ile) rs61740877 0.00235
NM_000875.5(IGF1R):c.1949G>A (p.Arg650Gln) rs61731172 0.00198
NM_000875.5(IGF1R):c.1162G>A (p.Val388Met) rs45445894 0.00183
NM_000875.5(IGF1R):c.2885+15A>G rs56141459 0.00174
NM_000875.5(IGF1R):c.3918C>T (p.Asp1306=) rs34364279 0.00130
NM_000875.5(IGF1R):c.1462+15C>G rs34313885 0.00118
NM_000875.5(IGF1R):c.3594C>T (p.Phe1198=) rs35701313 0.00104
NM_000875.5(IGF1R):c.3582C>T (p.Asp1194=) rs35362396 0.00098
NM_000875.5(IGF1R):c.1956T>G (p.Pro652=) rs45598332 0.00086
NM_000875.5(IGF1R):c.2570A>G (p.Asn857Ser) rs45611935 0.00067
NM_000875.5(IGF1R):c.1194C>T (p.Ser398=) rs35315829 0.00057
NM_000875.5(IGF1R):c.1773C>T (p.Asn591=) rs143045812 0.00057
NM_000875.5(IGF1R):c.3187-5C>T rs45495500 0.00052
NM_000875.5(IGF1R):c.588C>G (p.Thr196=) rs139571991 0.00035
NM_000875.5(IGF1R):c.3723-4G>A rs185740950 0.00017
NM_000875.5(IGF1R):c.4065C>T (p.Asn1355=) rs45453791 0.00015
NM_000875.5(IGF1R):c.1590-9G>A rs755331207 0.00013
NM_000875.5(IGF1R):c.3471G>A (p.Thr1157=) rs28664854 0.00013
NM_000875.5(IGF1R):c.4080G>A (p.Pro1360=) rs146862253 0.00009
NM_000875.5(IGF1R):c.2274G>A (p.Thr758=) rs572504542 0.00001
GRCh37/hg19 15q26.3(chr15:99191259-99193429)x1
GRCh37/hg19 15q26.3(chr15:99191259-99204652)x1
NM_000875.5(IGF1R):c.*63AG[3] rs370196264
NM_000875.5(IGF1R):c.1103-17A>G
NM_000875.5(IGF1R):c.1683C>T (p.Asp561=)
NM_000875.5(IGF1R):c.2202-18T>C
NM_000875.5(IGF1R):c.237G>A (p.Thr79=) rs34868731
NM_000875.5(IGF1R):c.237G>T (p.Thr79=) rs34868731
NM_000875.5(IGF1R):c.3255C>T (p.Gly1085=)
NM_000875.5(IGF1R):c.3458-20C>T
NM_000875.5(IGF1R):c.3477T>C (p.Asp1159=)
NM_000875.5(IGF1R):c.492G>T (p.Val164=)
NM_000875.5(IGF1R):c.795G>T (p.Pro265=)
NM_000875.5(IGF1R):c.885G>A (p.Gly295=) rs56303650

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