ClinVar Miner

List of variants in gene GALNT12 reported as benign for not provided

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_024642.5(GALNT12):c.372-94G>C rs2295922 0.95145
NM_024642.5(GALNT12):c.1458+58G>T rs1885608 0.72562
NM_024642.5(GALNT12):c.541+124C>T rs2295924 0.54681
NM_024642.5(GALNT12):c.1213-113C>G rs2277189 0.48192
NM_024642.5(GALNT12):c.541+285G>A rs2295925 0.40388
NM_024642.5(GALNT12):c.1212+178C>G rs10116756 0.31339
NM_024642.5(GALNT12):c.1458+189C>T rs10819379 0.17784
NM_024642.5(GALNT12):c.1036-42del rs3216734 0.16696
NM_024642.5(GALNT12):c.1459-234C>A rs10987952 0.11193
NM_024642.5(GALNT12):c.*171A>G rs2273847 0.09438
NM_024642.5(GALNT12):c.356A>T (p.Glu119Val) rs1137654 0.06543
NM_024642.5(GALNT12):c.542-304T>G rs34594897 0.05751
NM_024642.5(GALNT12):c.1344+61G>T rs3824516 0.04582
NM_024642.5(GALNT12):c.1459-327T>A rs75895880 0.04508
NM_024642.5(GALNT12):c.897A>G (p.Gln299=) rs16917929 0.04000
NM_024642.5(GALNT12):c.136G>A (p.Gly46Arg) rs10987768 0.02982
NM_024642.5(GALNT12):c.1459-105T>A rs73496194 0.02901
NM_024642.5(GALNT12):c.*67A>T rs78514784 0.02484
NM_024642.5(GALNT12):c.917+24C>T rs41297187 0.02396
NM_024642.5(GALNT12):c.1036-204A>G rs113675901 0.01878
NM_024642.5(GALNT12):c.1459-216G>A rs7853839 0.01598
NM_024642.5(GALNT12):c.1605+4G>A rs79574929 0.01136
NM_024642.5(GALNT12):c.781G>A (p.Asp261Asn) rs41306504 0.01010
NM_024642.5(GALNT12):c.375C>T (p.Cys125=) rs114902755 0.00634
NM_024642.5(GALNT12):c.579A>G (p.Gly193=) rs146370762 0.00613
NM_024642.5(GALNT12):c.1677C>T (p.Phe559=) rs112898261 0.00465
NM_024642.5(GALNT12):c.372-7T>A rs2295923 0.00235
NM_024642.5(GALNT12):c.1497C>T (p.Asn499=) rs35632007 0.00208
NM_024642.5(GALNT12):c.1301C>T (p.Pro434Leu) rs34565987 0.00117
NM_024642.5(GALNT12):c.138G>A (p.Gly46=) rs557604978 0.00107
NM_024642.5(GALNT12):c.567T>C (p.Asn189=) rs150417178 0.00062
NM_024642.5(GALNT12):c.840C>T (p.Asp280=) rs150946638 0.00054
NM_024642.5(GALNT12):c.372-14C>T rs185007553 0.00047
NM_024642.5(GALNT12):c.359G>C (p.Arg120Pro) rs202137559 0.00045
NM_024642.5(GALNT12):c.20G>T (p.Arg7Leu) rs568625965 0.00040
NM_024642.5(GALNT12):c.750G>A (p.Ser250=) rs146690078 0.00036
NM_024642.5(GALNT12):c.303C>G (p.His101Gln) rs201926457 0.00021
NM_024642.5(GALNT12):c.719C>T (p.Pro240Leu) rs59362219 0.00016
NM_024642.5(GALNT12):c.975G>A (p.Leu325=) rs140471094 0.00015
NM_024642.5(GALNT12):c.329G>A (p.Arg110His) rs374994372 0.00014
NM_024642.5(GALNT12):c.1131G>A (p.Leu377=) rs148125332 0.00013
NM_024642.5(GALNT12):c.814G>A (p.Gly272Arg) rs367645298 0.00006
NM_024642.5(GALNT12):c.504A>G (p.Leu168=) rs768255136 0.00004
NM_024642.5(GALNT12):c.909T>C (p.Asp303=) rs777028537 0.00003
NM_024642.5(GALNT12):c.831C>T (p.Gly277=) rs145133746 0.00002
NM_024642.5(GALNT12):c.837C>T (p.Phe279=) rs754951224 0.00001
NM_024642.5(GALNT12):c.1212+128A>T rs10119864
NM_024642.5(GALNT12):c.1344+135dup rs145380479
NM_024642.5(GALNT12):c.1392C>G (p.Pro464=) rs35616709
NM_024642.5(GALNT12):c.1392C>T (p.Pro464=) rs35616709
NM_024642.5(GALNT12):c.1707G>A (p.Ser569=) rs2273846
NM_024642.5(GALNT12):c.1707G>C (p.Ser569=) rs2273846
NM_024642.5(GALNT12):c.541+74G>T rs73496150
NM_024642.5(GALNT12):c.673A>T (p.Thr225Ser) rs531023279
NM_024642.5(GALNT12):c.732-171T>G rs2038622
NM_024642.5(GALNT12):c.732-229T>C rs2295926
NM_024642.5(GALNT12):c.903C>T (p.Pro301=) rs191834824
NM_024642.5(GALNT12):c.918-263A>C rs10819370

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