List of variants in gene SUFU reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 53

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.528C>T (p.His176=)	rs150569584	0.00148
NM_016169.4(SUFU):c.910+14C>T	rs202247757	0.00139
NM_016169.4(SUFU):c.*476A>G	rs575192580	0.00066
NM_016169.4(SUFU):c.*2729T>C	rs574630127	0.00045
NM_016169.4(SUFU):c.*2956C>T	rs562546771	0.00033
NM_016169.4(SUFU):c.*1936C>T	rs118033896	0.00027
NM_016169.4(SUFU):c.*1997A>G	rs757368847	0.00021
NM_016169.4(SUFU):c.1445C>T (p.Pro482Leu)	rs765358771	0.00020
NM_016169.4(SUFU):c.*721T>G	rs2298279	0.00014
NM_016169.4(SUFU):c.839G>A (p.Arg280Gln)	rs145704867	0.00014
NM_016169.4(SUFU):c.*1451C>T	rs886046659	0.00011
NM_016169.4(SUFU):c.*2195G>T	rs781227748	0.00010
NM_016169.4(SUFU):c.*907C>G	rs886046655	0.00008
NM_016169.4(SUFU):c.1028G>A (p.Arg343His)	rs79299301	0.00008
NM_016169.4(SUFU):c.*520G>A	rs757315966	0.00006
NM_016169.4(SUFU):c.992G>A (p.Arg331Gln)	rs141359583	0.00005
NM_016169.4(SUFU):c.*2267G>T	rs886046660	0.00004
NM_016169.4(SUFU):c.*2643C>G	rs886046663	0.00003
NM_016169.4(SUFU):c.*376G>A	rs866120174	0.00003
NM_016169.4(SUFU):c.*915G>C	rs886046656	0.00003
NM_016169.4(SUFU):c.*1908C>G	rs764234968	0.00002
NM_016169.4(SUFU):c.*3025T>C	rs896765914	0.00002
NM_016169.4(SUFU):c.*844G>A	rs1032441274	0.00002
NM_016169.4(SUFU):c.169A>G (p.Ile57Val)	rs377614167	0.00002
NM_016169.4(SUFU):c.*1145A>G	rs1190732664	0.00001
NM_016169.4(SUFU):c.*2278C>G	rs530131484	0.00001
NM_016169.4(SUFU):c.*2475C>T	rs886046661	0.00001
NM_016169.4(SUFU):c.*3045A>G	rs185874880	0.00001
NM_016169.4(SUFU):c.*305C>A	rs1430494184	0.00001
NM_016169.4(SUFU):c.*405G>A	rs2063829258	0.00001
NM_016169.4(SUFU):c.180C>T (p.Tyr60=)	rs776945270	0.00001
NM_016169.4(SUFU):c.183-13T>G	rs749913059	0.00001
NM_016169.4(SUFU):c.529A>G (p.Met177Val)	rs758672583	0.00001
NM_016169.4(SUFU):c.756+10G>C	rs764838079	0.00001
NM_016169.4(SUFU):c.*1104C>T	rs886046657
NM_016169.4(SUFU):c.*131C>G	rs886046654
NM_016169.4(SUFU):c.*1389C>T	rs886046658
NM_016169.4(SUFU):c.*138C>T	rs2063826618
NM_016169.4(SUFU):c.*1690A>G	rs955282121
NM_016169.4(SUFU):c.*1720C>G	rs536068954
NM_016169.4(SUFU):c.*1785C>T	rs1047091410
NM_016169.4(SUFU):c.*1889C>T	rs139020703
NM_016169.4(SUFU):c.*2479C>T	rs2063847339
NM_016169.4(SUFU):c.*2553T>C	rs886046662
NM_016169.4(SUFU):c.*2657T>C	rs2063848688
NM_016169.4(SUFU):c.*2757G>A	rs758662176
NM_016169.4(SUFU):c.*3110C>T	rs141940845
NM_016169.4(SUFU):c.*3239C>G	rs538132960
NM_016169.4(SUFU):c.3239_3241del	rs767259911
NM_016169.4(SUFU):c.*352C>G	rs139725961
NM_016169.4(SUFU):c.1174_1175dup (p.Arg393fs)	rs1564707343
NM_016169.4(SUFU):c.466T>C (p.Cys156Arg)	rs1554852266
NM_016169.4(SUFU):c.696C>G (p.Pro232=)	rs2063434189

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