ClinVar Miner

List of variants in gene ZNF469 reported by CeGaT Praxis fuer Humangenetik Tuebingen

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Total variants: 43
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HGVS dbSNP
NM_001127464.2(ZNF469):c.9011_9025delTTCCCGGGAACACCC (p.Leu3004_Thr3008del) rs281865162
NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=) rs273585633
NM_001367624.1(ZNF469):c.10361G>A (p.Arg3454Gln) rs75288466
NM_001367624.1(ZNF469):c.10518G>A (p.Pro3506=) rs376379111
NM_001367624.1(ZNF469):c.10656G>A (p.Pro3552=) rs191234581
NM_001367624.1(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834
NM_001367624.1(ZNF469):c.11107G>A (p.Val3703Met) rs151127652
NM_001367624.1(ZNF469):c.1346C>T (p.Pro449Leu) rs1388799029
NM_001367624.1(ZNF469):c.1471G>A (p.Ala491Thr) rs117555121
NM_001367624.1(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001367624.1(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001367624.1(ZNF469):c.1994C>T (p.Pro665Leu) rs184583062
NM_001367624.1(ZNF469):c.2699C>T (p.Pro900Leu) rs273585618
NM_001367624.1(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481
NM_001367624.1(ZNF469):c.3055C>T (p.Pro1019Ser) rs937180195
NM_001367624.1(ZNF469):c.3341G>T (p.Arg1114Leu) rs568046708
NM_001367624.1(ZNF469):c.362T>C (p.Ile121Thr) rs1555518437
NM_001367624.1(ZNF469):c.3759G>A (p.Ala1253=) rs543669472
NM_001367624.1(ZNF469):c.3773C>A (p.Ala1258Glu) rs141255631
NM_001367624.1(ZNF469):c.3931C>T (p.Pro1311Ser) rs187453092
NM_001367624.1(ZNF469):c.3950A>G (p.Lys1317Arg) rs772817384
NM_001367624.1(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076
NM_001367624.1(ZNF469):c.457C>A (p.Pro153Thr) rs532620482
NM_001367624.1(ZNF469):c.4778C>T (p.Ser1593Leu) rs768864900
NM_001367624.1(ZNF469):c.4910G>A (p.Arg1637Gln) rs273585621
NM_001367624.1(ZNF469):c.498C>G (p.Leu166=) rs1555518472
NM_001367624.1(ZNF469):c.5162G>T (p.Cys1721Phe) rs568197988
NM_001367624.1(ZNF469):c.5548C>A (p.Pro1850Thr) rs199932922
NM_001367624.1(ZNF469):c.5675G>A (p.Arg1892Lys) rs528085780
NM_001367624.1(ZNF469):c.6333C>T (p.Ala2111=) rs1039243677
NM_001367624.1(ZNF469):c.6599C>T (p.Thr2200Ile) rs1465493306
NM_001367624.1(ZNF469):c.6629T>C (p.Leu2210Pro) rs564413710
NM_001367624.1(ZNF469):c.725G>T (p.Ser242Ile) rs536586591
NM_001367624.1(ZNF469):c.7553C>A (p.Pro2518His) rs201943633
NM_001367624.1(ZNF469):c.7675A>G (p.Lys2559Glu) rs146789160
NM_001367624.1(ZNF469):c.7831G>A (p.Glu2611Lys) rs281865151
NM_001367624.1(ZNF469):c.8344C>T (p.His2782Tyr) rs553227769
NM_001367624.1(ZNF469):c.8705C>T (p.Thr2902Met) rs536725615
NM_001367624.1(ZNF469):c.9018C>T (p.Ala3006=) rs1048591670
NM_001367624.1(ZNF469):c.9055G>A (p.Glu3019Lys) rs765339766
NM_001367624.1(ZNF469):c.9673G>A (p.Ala3225Thr) rs1046436333
NM_001367624.1(ZNF469):c.9696G>A (p.Thr3232=) rs573582117
NM_001367624.1(ZNF469):c.98C>T (p.Pro33Leu) rs752770883

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