List of variants in gene MTAP reported as benign for bone disorder

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: 56

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HGVS	dbSNP	gnomAD frequency
NM_002451.4(MTAP):c.*3829T>C	rs6475592	0.44086
NM_002451.4(MTAP):c.*2365C>T	rs10117550	0.43789
NM_002451.4(MTAP):c.*884T>A	rs1134871	0.43727
NM_002451.4(MTAP):c.166G>A (p.Val56Ile)	rs7023954	0.42302
NM_002451.4(MTAP):c.*258A>C	rs15735	0.39404
NM_002451.4(MTAP):c.*2085G>A	rs10117507	0.24202
NM_002451.4(MTAP):c.*3093T>C	rs4977735	0.22251
NM_002451.4(MTAP):c.*2522A>G	rs3802394	0.21853
NM_002451.4(MTAP):c.*3946A>C	rs10965168	0.21553
NM_002451.4(MTAP):c.*536G>A	rs1134870	0.09270
NM_002451.4(MTAP):c.561C>T (p.Arg187=)	rs10965163	0.05936
NM_002451.4(MTAP):c.*797C>T	rs58555715	0.05202
NM_002451.4(MTAP):c.*3916C>T	rs80226037	0.02842
NM_002451.4(MTAP):c.*2539A>G	rs10123713	0.02420
NM_002451.4(MTAP):c.*2255A>G	rs79020697	0.02054
NM_002451.4(MTAP):c.*657T>C	rs146095448	0.01261
NM_002451.4(MTAP):c.*2873C>T	rs75664572	0.01200
NM_002451.4(MTAP):c.*3851C>G	rs76751525	0.01197
NM_002451.4(MTAP):c.*1181A>G	rs182505150	0.00948
NM_002451.4(MTAP):c.*3144G>A	rs148910202	0.00907
NM_002451.4(MTAP):c.*1341C>T	rs111408881	0.00815
NM_002451.4(MTAP):c.*1936C>T	rs117552951	0.00557
NM_002451.4(MTAP):c.*393G>C	rs78389853	0.00498
NM_002451.4(MTAP):c.768T>G (p.Pro256=)	rs62556500	0.00497
NM_002451.4(MTAP):c.*1643G>T	rs79546636	0.00491
NM_002451.4(MTAP):c.*3862C>T	rs560167088	0.00334
NM_002451.4(MTAP):c.*707A>G	rs138936486	0.00275
NM_002451.4(MTAP):c.*804T>C	rs142144597	0.00253
NM_002451.4(MTAP):c.*1038A>G	rs180861815	0.00242
NM_002451.4(MTAP):c.*3307G>T	rs41270139	0.00172
NM_002451.4(MTAP):c.*895G>A	rs41270137	0.00170
NM_002451.4(MTAP):c.691-13A>G	rs77412364	0.00087
NM_002451.4(MTAP):c.*328T>C	rs150414950	0.00068
NM_002451.4(MTAP):c.*2238C>T	rs150727017	0.00063
NM_002451.4(MTAP):c.*1065A>G	rs187215052	0.00049
NM_002451.4(MTAP):c.*1729G>A	rs182527165	0.00036
NM_002451.4(MTAP):c.653C>T (p.Ala218Val)	rs143080527	0.00031
NM_002451.4(MTAP):c.121-10T>C	rs201864201	0.00026
NM_002451.4(MTAP):c.179+12T>A	rs369294437	0.00025
NM_002451.4(MTAP):c.39A>C (p.Gly13=)	rs139020435	0.00023
NM_002451.4(MTAP):c.566G>T (p.Trp189Leu)	rs184520335	0.00019
NM_002451.4(MTAP):c.-5C>G	rs375344882	0.00010
NM_002451.4(MTAP):c.136A>C (p.Ile46Leu)	rs750076531	0.00009
NM_002451.4(MTAP):c.315C>T (p.Gly105=)	rs147319145	0.00006
NM_002451.4(MTAP):c.*2188C>T	rs117300281	0.00005
NM_002451.4(MTAP):c.603G>A (p.Glu201=)	rs189392570	0.00005
NM_002451.4(MTAP):c.*1225G>A	rs556119629	0.00004
NM_002451.4(MTAP):c.111A>G (p.Pro37=)	rs774955664	0.00004
NM_002451.4(MTAP):c.*606A>G	rs566061531	0.00003
NM_002451.4(MTAP):c.*17A>G	rs553057304	0.00001
NM_002451.4(MTAP):c.*15C>A	rs754086497
NM_002451.4(MTAP):c.*1622del	rs11358276
NM_002451.4(MTAP):c.*2279T>G	rs529226542
NM_002451.4(MTAP):c.*2348dup	rs397972510
NM_002451.4(MTAP):c.*259C>A	rs78195856
NM_002451.4(MTAP):c.*775dup	rs58147941

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