ClinVar Miner

List of variants in gene WHRN reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 112
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HGVS dbSNP gnomAD frequency
NM_015404.4(WHRN):c.2256= (p.Gln752=) rs6478078 0.99456
NM_015404.4(WHRN):c.1091= (p.His364=) rs10817610 0.98173
NM_015404.4(WHRN):c.1353T>C (p.Gly451=) rs4979387 0.76260
NM_015404.4(WHRN):c.1838T>C (p.Met613Thr) rs942519 0.47944
NM_015404.4(WHRN):c.2348T>C (p.Val783Ala) rs2274159 0.40624
NM_015404.4(WHRN):c.117G>A (p.Val39=) rs2297815 0.33019
NM_015404.4(WHRN):c.1627-12G>A rs2274160 0.23283
NM_015404.4(WHRN):c.1318G>A (p.Ala440Thr) rs4978584 0.19569
NM_015404.4(WHRN):c.2388C>A (p.Asn796Lys) rs2274158 0.19185
NM_015404.4(WHRN):c.2283C>T (p.Ser761=) rs34963246 0.12235
NM_015404.4(WHRN):c.1684C>G (p.Pro562Ala) rs12339210 0.09351
NM_015404.4(WHRN):c.1515G>A (p.Ala505=) rs34252199 0.03118
NM_015404.4(WHRN):c.1091A>G (p.His364Arg) rs10817610 0.01827
NM_015404.4(WHRN):c.229A>T (p.Thr77Ser) rs56204273 0.00613
NM_015404.4(WHRN):c.667C>T (p.Arg223Cys) rs76593842 0.00578
NM_015404.4(WHRN):c.2046G>C (p.Arg682=) rs35258467 0.00555
NM_015404.4(WHRN):c.2439G>A (p.Thr813=) rs61743618 0.00545
NM_015404.4(WHRN):c.2256G>C (p.Gln752His) rs6478078 0.00544
NM_015404.4(WHRN):c.764G>A (p.Gly255Asp) rs79509430 0.00475
NM_015404.4(WHRN):c.2586C>A (p.His862Gln) rs117592152 0.00424
NM_015404.4(WHRN):c.1454C>T (p.Pro485Leu) rs79572315 0.00364
NM_015404.4(WHRN):c.1365T>C (p.Ser455=) rs111033459 0.00294
NM_015404.4(WHRN):c.1627-5T>A rs187221008 0.00184
NM_015404.4(WHRN):c.1305C>T (p.Asn435=) rs150407952 0.00177
NM_015404.4(WHRN):c.1048C>T (p.Arg350Trp) rs142990800 0.00147
NM_015404.4(WHRN):c.19G>C (p.Gly7Arg) rs572671060 0.00141
NM_015404.4(WHRN):c.33C>G (p.Ser11Arg) rs45527543 0.00130
NM_015404.4(WHRN):c.668G>A (p.Arg223His) rs146273185 0.00122
NM_015404.4(WHRN):c.1352G>A (p.Gly451Asp) rs117352600 0.00120
NM_015404.4(WHRN):c.234G>A (p.Leu78=) rs148785227 0.00099
NM_015404.4(WHRN):c.75C>T (p.Gly25=) rs771128098 0.00099
NM_015404.4(WHRN):c.1149C>T (p.Thr383=) rs149558159 0.00098
NM_015404.4(WHRN):c.1992G>A (p.Pro664=) rs142568702 0.00084
NM_015404.4(WHRN):c.1135C>T (p.Arg379Trp) rs56059137 0.00083
NM_015404.4(WHRN):c.2027C>G (p.Pro676Arg) rs139279977 0.00067
NM_015404.4(WHRN):c.2322C>T (p.Ser774=) rs55966714 0.00062
NM_015404.4(WHRN):c.1455G>A (p.Pro485=) rs141807746 0.00055
NM_015404.4(WHRN):c.1075G>A (p.Val359Ile) rs147500559 0.00053
NM_015404.4(WHRN):c.191C>A (p.Ala64Asp) rs146655362 0.00053
NM_015404.4(WHRN):c.2510G>A (p.Arg837His) rs55749855 0.00053
NM_015404.4(WHRN):c.1148C>A (p.Thr383Asn) rs147283064 0.00052
NM_015404.4(WHRN):c.995G>A (p.Arg332Gln) rs139193948 0.00045
NM_015404.4(WHRN):c.1678G>A (p.Ala560Thr) rs182072601 0.00039
NM_015404.4(WHRN):c.2417C>T (p.Pro806Leu) rs149897775 0.00036
NM_015404.4(WHRN):c.1887G>A (p.Pro629=) rs143443833 0.00035
NM_015404.4(WHRN):c.1608C>G (p.Thr536=) rs139337135 0.00024
NM_015404.4(WHRN):c.1381A>C (p.Met461Leu) rs144878400 0.00022
NM_015404.4(WHRN):c.619G>T (p.Ala207Ser) rs111033469 0.00021
NM_015404.4(WHRN):c.2354C>T (p.Thr785Ile) rs201555289 0.00019
NM_015404.4(WHRN):c.2060C>T (p.Pro687Leu) rs534523640 0.00014
NM_015404.4(WHRN):c.2112G>T (p.Leu704=) rs535492772 0.00011
NM_015404.4(WHRN):c.998G>A (p.Ser333Asn) rs200073414 0.00011
NM_015404.4(WHRN):c.1625G>A (p.Arg542Lys) rs200040563 0.00010
NM_015404.4(WHRN):c.1696G>C (p.Val566Leu) rs189654215 0.00010
NM_015404.4(WHRN):c.2384G>A (p.Arg795Gln) rs143763650 0.00010
NM_015404.4(WHRN):c.409G>C (p.Glu137Gln) rs41297175 0.00010
NM_015404.4(WHRN):c.1222C>A (p.Pro408Thr) rs368241259 0.00009
NM_015404.4(WHRN):c.1611C>T (p.Thr537=) rs201280818 0.00009
NM_015404.4(WHRN):c.1349G>A (p.Arg450His) rs200377723 0.00007
NM_015404.4(WHRN):c.1716C>T (p.Thr572=) rs760471578 0.00007
NM_015404.4(WHRN):c.1677C>T (p.Asn559=) rs138127153 0.00005
NM_015404.4(WHRN):c.1176C>T (p.Gly392=) rs200276167 0.00004
NM_015404.4(WHRN):c.1417-8G>A rs202228471 0.00004
NM_015404.4(WHRN):c.2073C>T (p.Ser691=) rs768690928 0.00004
NM_015404.4(WHRN):c.2085G>A (p.Glu695=) rs140043085 0.00004
NM_015404.4(WHRN):c.2193C>T (p.Ser731=) rs147358257 0.00004
NM_015404.4(WHRN):c.2203G>A (p.Val735Ile) rs373552185 0.00004
NM_015404.4(WHRN):c.1596C>T (p.His532=) rs775240892 0.00003
NM_015404.4(WHRN):c.2029A>G (p.Ile677Val) rs758287560 0.00003
NM_015404.4(WHRN):c.35C>T (p.Ser12Leu) rs760261757 0.00003
NM_015404.4(WHRN):c.44C>T (p.Thr15Ile) rs727502957 0.00003
NM_015404.4(WHRN):c.1291C>T (p.Arg431Trp) rs397517256 0.00002
NM_015404.4(WHRN):c.1360G>A (p.Val454Ile) rs370178817 0.00002
NM_015404.4(WHRN):c.139A>G (p.Thr47Ala) rs556585167 0.00002
NM_015404.4(WHRN):c.2293G>C (p.Gly765Arg) rs142685292 0.00002
NM_015404.4(WHRN):c.2645G>A (p.Arg882His) rs760928525 0.00002
NM_015404.4(WHRN):c.1547C>T (p.Thr516Ile) rs756090687 0.00001
NM_015404.4(WHRN):c.1578T>C (p.Gly526=) rs111033438 0.00001
NM_015404.4(WHRN):c.1725G>A (p.Gly575=) rs1333495064 0.00001
NM_015404.4(WHRN):c.1833C>T (p.Ser611=) rs752505729 0.00001
NM_015404.4(WHRN):c.2056C>A (p.Pro686Thr) rs201690920 0.00001
NM_015404.4(WHRN):c.2284G>A (p.Glu762Lys) rs757731586 0.00001
NM_015404.4(WHRN):c.376G>A (p.Ala126Thr) rs1444564272 0.00001
NM_015404.4(WHRN):c.690C>T (p.Thr230=) rs779112096 0.00001
NM_015404.4(WHRN):c.725G>A (p.Arg242His) rs727505127 0.00001
NC_000009.12:g.(?_114402754)_(114504801_?)dup
NM_015404.4(WHRN):c.1126G>T (p.Ala376Ser) rs545251395
NM_015404.4(WHRN):c.1158C>G (p.Asn386Lys) rs397517253
NM_015404.4(WHRN):c.1251C>T (p.Ser417=) rs1554719002
NM_015404.4(WHRN):c.1267C>T (p.Arg423Ter) rs397517255
NM_015404.4(WHRN):c.14T>C (p.Leu5Pro) rs1554747807
NM_015404.4(WHRN):c.1542G>A (p.Gly514=) rs397517257
NM_015404.4(WHRN):c.1626+9C>A rs727504908
NM_015404.4(WHRN):c.1824G>A (p.Gln608=) rs755074681
NM_015404.4(WHRN):c.2333G>A (p.Arg778Gln) rs727505188
NM_015404.4(WHRN):c.2364G>T (p.Arg788Ser) rs1441372523
NM_015404.4(WHRN):c.2418+3G>A rs876657772
NM_015404.4(WHRN):c.2455G>A (p.Val819Met) rs1589057203
NM_015404.4(WHRN):c.2569C>T (p.Gln857Ter) rs727504817
NM_015404.4(WHRN):c.2621G>C (p.Gly874Ala) rs756466784
NM_015404.4(WHRN):c.2644C>T (p.Arg882Cys) rs150586098
NM_015404.4(WHRN):c.2722T>C (p.Ter908Gln) rs727505255
NM_015404.4(WHRN):c.328A>G (p.Thr110Ala) rs572312301
NM_015404.4(WHRN):c.427T>C (p.Leu143=) rs727502956
NM_015404.4(WHRN):c.640C>G (p.Leu214Val) rs1554735418
NM_015404.4(WHRN):c.643del (p.Val215fs) rs397517258
NM_015404.4(WHRN):c.676G>C (p.Gly226Arg) rs727502955
NM_015404.4(WHRN):c.744G>A (p.Ser248=) rs397517259
NM_015404.4(WHRN):c.75CGG[2] (p.Gly29del) rs757435431
NM_015404.4(WHRN):c.914A>G (p.Tyr305Cys) rs1589199689
NM_015404.4(WHRN):c.943G>C (p.Ala315Pro) rs876657774
NM_015404.4(WHRN):c.955G>T (p.Gly319Trp) rs143165834

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