ClinVar Miner

List of variants reported as uncertain significance for Symmetrical dyschromatosis of extremities by Illumina Laboratory Services, Illumina

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ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_001111.5(ADAR):c.*2586C>T rs559398617 0.00042
NM_001111.5(ADAR):c.*1751T>G rs748291356 0.00040
NM_001111.5(ADAR):c.*301C>T rs986381538 0.00020
NM_001111.5(ADAR):c.*612A>T rs985271768 0.00011
NM_001111.5(ADAR):c.*323G>C rs886045334 0.00010
NM_001111.5(ADAR):c.*60G>A rs772429851 0.00010
NM_001111.5(ADAR):c.1392T>C (p.Asn464=) rs370763473 0.00009
NM_001111.5(ADAR):c.*884C>T rs556661959 0.00006
NM_001111.5(ADAR):c.*1344G>A rs550673541 0.00005
NM_001111.5(ADAR):c.*885G>A rs149774073 0.00005
NM_001111.5(ADAR):c.2080C>T (p.Pro694Ser) rs755535385 0.00005
NM_001111.5(ADAR):c.*2316G>A rs200367762 0.00004
NM_001111.5(ADAR):c.*2317C>T rs367964862 0.00004
NM_001111.5(ADAR):c.*590G>A rs908072891 0.00004
NM_001111.5(ADAR):c.*989C>T rs1485739737 0.00004
NM_001111.5(ADAR):c.-85G>A rs1470901197 0.00004
NM_001111.5(ADAR):c.2762+10G>A rs879809934 0.00004
NM_001111.5(ADAR):c.*1406A>C rs886045325 0.00003
NM_001111.5(ADAR):c.*468G>A rs886045332 0.00003
NM_001111.5(ADAR):c.*1728C>T rs886045322 0.00002
NM_001111.5(ADAR):c.*2636G>A rs1019588923 0.00002
NM_001111.5(ADAR):c.*317T>G rs886045335 0.00002
NM_001111.5(ADAR):c.*319del rs774214510 0.00002
NM_001111.5(ADAR):c.-154C>T rs1470021699 0.00002
NM_001111.5(ADAR):c.3519C>T (p.Tyr1173=) rs755264415 0.00002
NM_001111.5(ADAR):c.*1454C>G rs967668970 0.00001
NM_001111.5(ADAR):c.*1871A>G rs1228582826 0.00001
NM_001111.5(ADAR):c.*479T>C rs185835529 0.00001
NM_001111.5(ADAR):c.*527A>G rs886045330 0.00001
NM_001111.5(ADAR):c.*812C>T rs747246150 0.00001
NM_001111.5(ADAR):c.*825G>A rs145743236 0.00001
NM_001111.5(ADAR):c.-71T>C rs886045346 0.00001
NM_001111.5(ADAR):c.1097A>G (p.Lys366Arg) rs770795921 0.00001
NM_001111.5(ADAR):c.1189T>A (p.Ser397Thr) rs1190740301 0.00001
NM_001111.5(ADAR):c.2415A>G (p.Thr805=) rs1298874562 0.00001
NM_001111.5(ADAR):c.2920A>G (p.Lys974Glu) rs886045339 0.00001
NM_001111.5(ADAR):c.3645C>G (p.Pro1215=) rs886045338 0.00001
NM_001111.5(ADAR):c.*1036C>G rs886045327
NM_001111.5(ADAR):c.*1104T>C rs886045326
NM_001111.5(ADAR):c.*110dup rs886045337
NM_001111.5(ADAR):c.*1192C>T rs931843098
NM_001111.5(ADAR):c.*1221C>T rs1696549699
NM_001111.5(ADAR):c.*1322A>G rs1237025828
NM_001111.5(ADAR):c.*1336A>G rs1385402270
NM_001111.5(ADAR):c.*1566T>G rs886045324
NM_001111.5(ADAR):c.*1712C>G rs886045323
NM_001111.5(ADAR):c.*1799_*1800del rs886045321
NM_001111.5(ADAR):c.*1919T>G rs1198048286
NM_001111.5(ADAR):c.*206T>G rs886045336
NM_001111.5(ADAR):c.*2134T>C rs1696483286
NM_001111.5(ADAR):c.*2153T>C rs1696482158
NM_001111.5(ADAR):c.*2323_*2330dup rs113414804
NM_001111.5(ADAR):c.*2727dup rs754401167
NM_001111.5(ADAR):c.*361C>G rs886045333
NM_001111.5(ADAR):c.*519del rs886045331
NM_001111.5(ADAR):c.*714G>A rs886045329
NM_001111.5(ADAR):c.*749G>A rs886045328
NM_001111.5(ADAR):c.1113T>C (p.Ser371=) rs780284489
NM_001111.5(ADAR):c.1300C>T (p.Pro434Ser) rs749677748
NM_001111.5(ADAR):c.1372G>A (p.Asp458Asn) rs759763367
NM_001111.5(ADAR):c.1402G>T (p.Ala468Ser) rs761708272
NM_001111.5(ADAR):c.1405G>T (p.Ala469Ser) rs886045343
NM_001111.5(ADAR):c.1450A>G (p.Ser484Gly) rs886045342
NM_001111.5(ADAR):c.1910A>G (p.Lys637Arg) rs886045341
NM_001111.5(ADAR):c.224T>G (p.Phe75Cys) rs886045345
NM_001111.5(ADAR):c.2270+10C>T rs1697527897
NM_001111.5(ADAR):c.2306T>C (p.Phe769Ser) rs886045340
NM_001111.5(ADAR):c.2330A>G (p.Lys777Arg) rs1197574959
NM_001111.5(ADAR):c.2763-7T>C rs1696928206
NM_001111.5(ADAR):c.3081C>T (p.Leu1027=) rs145851568
NM_001111.5(ADAR):c.3432C>G (p.Gly1144=) rs568610646
NM_001111.5(ADAR):c.3499A>C (p.Lys1167Gln) rs1571045177
NM_001111.5(ADAR):c.3520C>G (p.Arg1174Gly) rs1243173166
NM_001111.5(ADAR):c.394G>A (p.Glu132Lys) rs1697933888
NM_001111.5(ADAR):c.739G>A (p.Ala247Thr) rs886045344
NM_001111.5(ADAR):c.751C>G (p.Gln251Glu) rs777881995
NM_001111.5(ADAR):c.866A>G (p.Asp289Gly) rs1697896792

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