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

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_031844.3(HNRNPU):c.261G>A (p.Glu87=)	rs6675421	0.28876
NM_031844.3(HNRNPU):c.877+71T>A	rs12124462	0.28294
NM_031844.3(HNRNPU):c.1495-113G>C	rs9730334	0.21984
NM_031844.3(HNRNPU):c.1017+326C>T	rs12069105	0.21897
NM_031844.3(HNRNPU):c.1615-127A>G	rs1874393	0.15445
NM_031844.3(HNRNPU):c.877+70G>A	rs58736171	0.13488
NM_031844.3(HNRNPU):c.2352+102G>T	rs10927336	0.13048
NM_031844.3(HNRNPU):c.1017+272G>A	rs12079538	0.12535
NM_031844.3(HNRNPU):c.1117+24T>G	rs73128486	0.06036
NM_031844.3(HNRNPU):c.1615-209C>T	rs76169958	0.05593
NM_031844.3(HNRNPU):c.1231-200T>A	rs112642178	0.02318
NM_031844.3(HNRNPU):c.1117+153G>A	rs79834162	0.02311
NM_031844.3(HNRNPU):c.2352+14A>T	rs57080269	0.02263
NM_031844.3(HNRNPU):c.803+11C>T	rs74152197	0.01825
NC_000001.11:g.244864715T>G	rs116239278	0.01790
NM_031844.3(HNRNPU):c.2169C>T (p.Ala723=)	rs11537737	0.00657
NM_031844.3(HNRNPU):c.141C>T (p.Ala47=)	rs111518952	0.00536
NM_031844.3(HNRNPU):c.1743+10A>C	rs75053711	0.00248
NM_031844.3(HNRNPU):c.-41G>A	rs376110167	0.00168
NM_031844.3(HNRNPU):c.1215G>A (p.Val405=)	rs147232928	0.00161
NM_031844.3(HNRNPU):c.507G>A (p.Gln169=)	rs139561508	0.00049
NM_031844.3(HNRNPU):c.1251A>G (p.Val417=)	rs142767399	0.00045
NM_031844.3(HNRNPU):c.1208A>C (p.Asn403Thr)	rs767181341	0.00006
NM_031844.3(HNRNPU):c.1460G>C (p.Gly487Ala)	rs199740131	0.00005
NM_031844.3(HNRNPU):c.2424+16T>C	rs537512846	0.00002
NM_031844.3(HNRNPU):c.2193T>C (p.Asn731=)	rs372228779	0.00001
NM_031844.3(HNRNPU):c.877+47T>G	rs372227800	0.00001
NM_031844.2(HNRNPU):c.2166_2167+1delAGG	rs575582638
NM_031844.3(HNRNPU):c.1118-30C>A	rs145042684
NM_031844.3(HNRNPU):c.1494+21del	rs750413170
NM_031844.3(HNRNPU):c.2167+39C>A	rs190132789
NM_031844.3(HNRNPU):c.2353-114_2353-111del	rs59942516
NM_031844.3(HNRNPU):c.878-9T>C	rs573967558

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