ClinVar Miner

List of variants in gene IFT172 reported as benign

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_015662.3(IFT172):c.2116-254A>G rs780108 0.57077
NM_015662.3(IFT172):c.2115+180C>T rs780110 0.55766
NM_015662.3(IFT172):c.2116-31T>C rs780107 0.47348
NM_015662.3(IFT172):c.1692+310A>G rs1647266 0.47341
NM_015662.3(IFT172):c.3372-164C>T rs780104 0.47338
NM_015662.3(IFT172):c.1829+12G>A rs1647276 0.47329
NM_015662.3(IFT172):c.402+99A>G rs2272417 0.39095
NM_015662.3(IFT172):c.4659+75C>T rs11126999 0.37630
NM_015662.3(IFT172):c.3372-236G>A rs79740025 0.11750
NM_015662.3(IFT172):c.3372-251G>A rs6734392 0.08432
NM_015662.3(IFT172):c.39+74G>A rs7583698 0.07849
NM_015662.3(IFT172):c.1326-196G>A rs56047188 0.06870
NM_015662.3(IFT172):c.3466-56T>C rs10166551 0.03786
NM_015662.3(IFT172):c.2877+249C>T rs704792 0.03745
NM_015662.3(IFT172):c.1829+37G>C rs1647275 0.03744
NM_015662.3(IFT172):c.1830-98G>T rs139218763 0.03132
NM_015662.3(IFT172):c.571-194A>G rs111315397 0.02879
NM_015662.3(IFT172):c.337-12C>T rs79529534 0.02365
NM_015662.3(IFT172):c.571-15C>G rs75809198 0.01015
NM_015662.3(IFT172):c.1338T>C (p.Asn446=) rs61743327 0.00780
NM_015662.3(IFT172):c.2858G>A (p.Arg953His) rs704793 0.00606
NM_015662.3(IFT172):c.3401G>T (p.Arg1134Leu) rs148624326 0.00526
NM_015662.3(IFT172):c.4272G>A (p.Gln1424=) rs147850047 0.00526
NM_015662.3(IFT172):c.4428+5C>G rs114235369 0.00521
NM_015662.3(IFT172):c.4659+16T>C rs143060452 0.00514
NM_015662.3(IFT172):c.1685C>G (p.Thr562Ser) rs61743977 0.00470
NM_015662.3(IFT172):c.4540-6C>T rs146140583 0.00361
NM_015662.3(IFT172):c.3357C>T (p.His1119=) rs76787560 0.00238
NM_015662.3(IFT172):c.3073C>G (p.Pro1025Ala) rs61747068 0.00152
NM_015662.3(IFT172):c.2443-19A>G rs199907803 0.00101
NM_015662.3(IFT172):c.402+8A>C rs184565714 0.00083
NM_015662.3(IFT172):c.1433A>T (p.Asn478Ile) rs143491198 0.00061
NM_015662.3(IFT172):c.3474C>T (p.Phe1158=) rs534566990 0.00035
NM_015662.3(IFT172):c.915A>G (p.Thr305=) rs180855666 0.00006
NM_015662.3(IFT172):c.1168-7G>A rs373380537 0.00005
NM_015662.3(IFT172):c.4628C>T (p.Thr1543Met) rs571220836 0.00004
NM_015662.3(IFT172):c.666T>C (p.Tyr222=) rs753217975 0.00001
NM_015662.3(IFT172):c.1459C>T (p.Arg487Cys)
NM_015662.3(IFT172):c.1524+211del rs34330432
NM_015662.3(IFT172):c.1525-17G>A rs187471043
NM_015662.3(IFT172):c.1525-6C>G rs201231401
NM_015662.3(IFT172):c.1525-6C>T
NM_015662.3(IFT172):c.184-14_184-11del
NM_015662.3(IFT172):c.184-23dup rs747166252
NM_015662.3(IFT172):c.2023-5dup
NM_015662.3(IFT172):c.2877+48T>G rs780106
NM_015662.3(IFT172):c.4660-153dup rs11430923
NM_015662.3(IFT172):c.570+269_570+270dup rs10651081
NM_015662.3(IFT172):c.570+269dup rs10651081
NM_015662.3(IFT172):c.571-193TG[13] rs71401571
NM_015662.3(IFT172):c.571-193TG[15] rs71401571

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