ClinVar Miner

List of variants in gene WDR62 reported by CeGaT Center for Human Genetics Tuebingen

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) rs62109744 0.00795
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023 0.00416
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912 0.00414
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) rs111294536 0.00310
NM_001083961.2(WDR62):c.4312-5T>G rs182467995 0.00215
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=) rs149289227 0.00183
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) rs146274964 0.00161
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) rs117887683 0.00078
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) rs146180208 0.00075
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=) rs144697999 0.00073
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168 0.00066
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186 0.00041
NM_001083961.2(WDR62):c.82C>T (p.Arg28Trp) rs200283315 0.00038
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=) rs757294519 0.00035
NM_001083961.2(WDR62):c.546C>T (p.Asn182=) rs199931318 0.00026
NM_001083961.2(WDR62):c.820T>G (p.Tyr274Asp) rs746156911 0.00021
NM_001083961.2(WDR62):c.4312T>A (p.Leu1438Met) rs138814793 0.00019
NM_001083961.2(WDR62):c.1233+7C>G rs537771936 0.00017
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=) rs373906889 0.00013
NM_001083961.2(WDR62):c.10G>C (p.Val4Leu) rs147077663 0.00012
NM_001083961.2(WDR62):c.328G>A (p.Ala110Thr) rs200316266 0.00011
NM_001083961.2(WDR62):c.1043+3A>G rs587784541 0.00009
NM_001083961.2(WDR62):c.4122C>T (p.Gly1374=) rs773948810 0.00008
NM_001083961.2(WDR62):c.2560G>A (p.Ala854Thr) rs368030329 0.00007
NM_001083961.2(WDR62):c.1031G>A (p.Gly344Asp) rs141927841 0.00006
NM_001083961.2(WDR62):c.1640C>T (p.Thr547Met) rs756313871 0.00005
NM_001083961.2(WDR62):c.216C>T (p.Asn72=) rs370507238 0.00004
NM_001083961.2(WDR62):c.4329G>A (p.Gln1443=) rs771131709 0.00004
NM_001083961.2(WDR62):c.3810C>T (p.Thr1270=) rs765881142 0.00003
NM_001083961.2(WDR62):c.4296C>T (p.Leu1432=) rs765001215 0.00003
NM_001083961.2(WDR62):c.1764C>T (p.Phe588=) rs757137989 0.00001
NM_001083961.2(WDR62):c.2269C>G (p.Leu757Val) rs150593960 0.00001
NM_001083961.2(WDR62):c.2674G>A (p.Glu892Lys) rs1349805169 0.00001
NM_001083961.2(WDR62):c.3874G>A (p.Glu1292Lys) rs1447628516 0.00001
NM_001083961.2(WDR62):c.4033C>T (p.Arg1345Cys) rs201363122 0.00001
NM_001083961.2(WDR62):c.700G>T (p.Val234Leu) rs1216375665 0.00001
GRCh37/hg19 19q13.12(chr19:36572335-36574143)x3
NM_001083961.2(WDR62):c.1129G>T (p.Val377Leu) rs761204875
NM_001083961.2(WDR62):c.1233+7C>A rs537771936
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1838G>T (p.Gly613Val) rs1599812719
NM_001083961.2(WDR62):c.2263del (p.His755fs) rs1064797237
NM_001083961.2(WDR62):c.2763C>G (p.Gly921=)
NM_001083961.2(WDR62):c.2864_2867del (p.Asp955fs) rs757827840
NM_001083961.2(WDR62):c.327C>T (p.Thr109=)
NM_001083961.2(WDR62):c.3309C>A (p.Phe1103Leu) rs1064797238
NM_001083961.2(WDR62):c.3336-5C>A rs587784555
NM_001083961.2(WDR62):c.3351C>T (p.Phe1117=)
NM_001083961.2(WDR62):c.3451G>C (p.Asp1151His)
NM_001083961.2(WDR62):c.3702C>T (p.Leu1234=) rs143638774
NM_001083961.2(WDR62):c.4345C>T (p.Gln1449Ter) rs1301404126
NM_001083961.2(WDR62):c.4383G>C (p.Trp1461Cys)
NM_001083961.2(WDR62):c.4553G>C (p.Arg1518Thr)
NM_001083961.2(WDR62):c.553G>A (p.Asp185Asn) rs1393055537
NM_001083961.2(WDR62):c.600_601del (p.Arg200fs)
NM_001083961.2(WDR62):c.761TCT[1] (p.Phe255del) rs1064797236

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