ClinVar Miner

List of variants in gene MTAP reported as benign for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_002451.4(MTAP):c.*1038A>G rs180861815
NM_002451.4(MTAP):c.*1065A>G rs187215052
NM_002451.4(MTAP):c.*1181A>G rs182505150
NM_002451.4(MTAP):c.*1225G>A rs556119629
NM_002451.4(MTAP):c.*1341C>T rs111408881
NM_002451.4(MTAP):c.*15C>A
NM_002451.4(MTAP):c.*1622del rs11358276
NM_002451.4(MTAP):c.*1643G>T rs79546636
NM_002451.4(MTAP):c.*1729G>A rs182527165
NM_002451.4(MTAP):c.*17A>G rs553057304
NM_002451.4(MTAP):c.*1936C>T rs117552951
NM_002451.4(MTAP):c.*2085G>A rs10117507
NM_002451.4(MTAP):c.*2188C>T
NM_002451.4(MTAP):c.*2238C>T rs150727017
NM_002451.4(MTAP):c.*2255A>G rs79020697
NM_002451.4(MTAP):c.*2279T>G rs529226542
NM_002451.4(MTAP):c.*2348dup rs397972510
NM_002451.4(MTAP):c.*2365C>T rs10117550
NM_002451.4(MTAP):c.*2522A>G rs3802394
NM_002451.4(MTAP):c.*2539A>G rs10123713
NM_002451.4(MTAP):c.*258A>C rs15735
NM_002451.4(MTAP):c.*259C>A rs78195856
NM_002451.4(MTAP):c.*2873C>T rs75664572
NM_002451.4(MTAP):c.*3093T>C rs4977735
NM_002451.4(MTAP):c.*3144G>A rs148910202
NM_002451.4(MTAP):c.*328T>C rs150414950
NM_002451.4(MTAP):c.*3307G>T rs41270139
NM_002451.4(MTAP):c.*3829T>C rs6475592
NM_002451.4(MTAP):c.*3851C>G rs76751525
NM_002451.4(MTAP):c.*3862C>T rs560167088
NM_002451.4(MTAP):c.*3916C>T rs80226037
NM_002451.4(MTAP):c.*393G>C rs78389853
NM_002451.4(MTAP):c.*3946A>C rs10965168
NM_002451.4(MTAP):c.*536G>A rs1134870
NM_002451.4(MTAP):c.*606A>G rs566061531
NM_002451.4(MTAP):c.*657T>C rs146095448
NM_002451.4(MTAP):c.*707A>G rs138936486
NM_002451.4(MTAP):c.*775dup rs58147941
NM_002451.4(MTAP):c.*797C>T rs58555715
NM_002451.4(MTAP):c.*804T>C rs142144597
NM_002451.4(MTAP):c.*884T>A rs1134871
NM_002451.4(MTAP):c.*895G>A rs41270137
NM_002451.4(MTAP):c.-5C>G rs375344882
NM_002451.4(MTAP):c.111A>G (p.Pro37=)
NM_002451.4(MTAP):c.121-10T>C rs201864201
NM_002451.4(MTAP):c.136A>C (p.Ile46Leu)
NM_002451.4(MTAP):c.166G>A (p.Val56Ile) rs7023954
NM_002451.4(MTAP):c.179+12T>A rs369294437
NM_002451.4(MTAP):c.315C>T (p.Gly105=) rs147319145
NM_002451.4(MTAP):c.39A>C (p.Gly13=) rs139020435
NM_002451.4(MTAP):c.561C>T (p.Arg187=) rs10965163
NM_002451.4(MTAP):c.566G>T (p.Trp189Leu) rs184520335
NM_002451.4(MTAP):c.603G>A (p.Glu201=) rs189392570
NM_002451.4(MTAP):c.653C>T (p.Ala218Val) rs143080527
NM_002451.4(MTAP):c.691-13A>G rs77412364
NM_002451.4(MTAP):c.768T>G (p.Pro256=) rs62556500

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