ClinVar Miner

List of variants in gene PTPN23 reported as benign for not provided

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_015466.4(PTPN23):c.2799G>A (p.Pro933=) rs900689 0.95645
NM_015466.4(PTPN23):c.987T>C (p.Thr329=) rs900688 0.95444
NM_015466.4(PTPN23):c.3498G>A (p.Glu1166=) rs1531875 0.49055
NM_015466.4(PTPN23):c.2130-7C>T rs3736177 0.36872
NM_015466.4(PTPN23):c.2830G>A (p.Ala944Thr) rs6780013 0.34529
NM_015466.4(PTPN23):c.4655T>C (p.Leu1552Pro) rs150037620 0.01798
NM_015466.4(PTPN23):c.891G>A (p.Ala297=) rs79728008 0.01463
NM_015466.4(PTPN23):c.2350C>T (p.Pro784Ser) rs116305269 0.01124
NM_015466.4(PTPN23):c.3388G>A (p.Gly1130Ser) rs138329311 0.00677
NM_015466.4(PTPN23):c.3295C>T (p.Pro1099Ser) rs149563514 0.00668
NM_015466.4(PTPN23):c.1628C>T (p.Pro543Leu) rs145771357 0.00614
NM_015466.4(PTPN23):c.365-14C>T rs139593091 0.00551
NM_015466.4(PTPN23):c.627+8C>T rs72911279 0.00398
NM_015466.4(PTPN23):c.781G>A (p.Glu261Lys) rs147122610 0.00384
NM_015466.4(PTPN23):c.3429C>T (p.Pro1143=) rs114781181 0.00312
NM_015466.4(PTPN23):c.2068C>T (p.Leu690=) rs116521545 0.00309
NM_015466.4(PTPN23):c.2148G>A (p.Pro716=) rs150385027 0.00259
NM_015466.4(PTPN23):c.1113G>A (p.Leu371=) rs143729247 0.00231
NM_015466.4(PTPN23):c.4910G>A (p.Ter1637=) rs142269660 0.00215
NM_015466.4(PTPN23):c.4149G>T (p.Pro1383=) rs147959396 0.00197
NM_015466.4(PTPN23):c.693C>T (p.Gly231=) rs145933393 0.00145
NM_015466.4(PTPN23):c.2490G>T (p.Glu830Asp) rs117855006 0.00140
NM_015466.4(PTPN23):c.3545G>A (p.Arg1182Gln) rs148987427 0.00113
NM_015466.4(PTPN23):c.4179-5C>T rs112931729 0.00110
NM_015466.4(PTPN23):c.1642+14G>A rs138693429 0.00091
NM_015466.4(PTPN23):c.4578C>A (p.Pro1526=) rs144497417 0.00077
NM_015466.4(PTPN23):c.2375C>T (p.Pro792Leu) rs374555949 0.00070
NM_015466.4(PTPN23):c.1387T>C (p.Leu463=) rs149474517 0.00064
NM_015466.4(PTPN23):c.4360G>A (p.Glu1454Lys) rs199529980 0.00038
NM_015466.4(PTPN23):c.3956C>T (p.Ala1319Val) rs150134286 0.00035
NM_015466.4(PTPN23):c.415-13C>T rs200367977 0.00034
NM_015466.4(PTPN23):c.2040A>C (p.Ala680=) rs570452002 0.00029
NM_015466.4(PTPN23):c.3298C>T (p.Arg1100Cys) rs201946361 0.00024
NM_015466.4(PTPN23):c.287+9C>T rs200788331 0.00022
NM_015466.4(PTPN23):c.1004-15T>C rs149865007 0.00019
NM_015466.4(PTPN23):c.993G>A (p.Gln331=) rs145629019 0.00015
NM_015466.4(PTPN23):c.2136G>A (p.Leu712=) rs539926264 0.00011
NM_015466.4(PTPN23):c.1653C>T (p.Ala551=) rs141629698 0.00009
NM_015466.4(PTPN23):c.4106G>A (p.Arg1369His) rs201950738 0.00009
NM_015466.4(PTPN23):c.546+10C>T rs200803095 0.00007
NM_015466.4(PTPN23):c.4576C>A (p.Pro1526Thr) rs138389235 0.00005
NM_015466.4(PTPN23):c.3357G>A (p.Leu1119=) rs545969329 0.00003
NM_015466.4(PTPN23):c.3774G>A (p.Pro1258=) rs144028724 0.00001
NM_015466.4(PTPN23):c.499G>A (p.Val167Ile) rs377445101 0.00001
NM_015466.4(PTPN23):c.1003+23dup
NM_015466.4(PTPN23):c.1003+7dup
NM_015466.4(PTPN23):c.1004-3del rs527516177
NM_015466.4(PTPN23):c.1004-3dup rs527516177
NM_015466.4(PTPN23):c.1569C>T (p.Val523=)
NM_015466.4(PTPN23):c.159+24del rs746022578
NM_015466.4(PTPN23):c.160-3del
NM_015466.4(PTPN23):c.160-3dup rs775683268
NM_015466.4(PTPN23):c.1798-14dup
NM_015466.4(PTPN23):c.2248C>G (p.Pro750Ala)
NM_015466.4(PTPN23):c.3886_3888del (p.Lys1296del) rs751809435
NM_015466.4(PTPN23):c.4614C>G (p.Thr1538=) rs535502642
NM_015466.4(PTPN23):c.4635G>A (p.Pro1545=) rs6789730
NM_015466.4(PTPN23):c.760-20C>T rs201260277
NM_015466.4(PTPN23):c.807+21del rs2107715845

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