ClinVar Miner

List of variants in gene TP63 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_003722.5(TP63):c.*1130_*1133del rs886058229
NM_003722.5(TP63):c.*1164A>G rs886058230
NM_003722.5(TP63):c.*1181T>C rs565556454
NM_003722.5(TP63):c.*1217T>C rs886058231
NM_003722.5(TP63):c.*1472A>G rs375551286
NM_003722.5(TP63):c.*1702G>A rs886058232
NM_003722.5(TP63):c.*1846C>T rs886058234
NM_003722.5(TP63):c.*1947dup rs140654135
NM_003722.5(TP63):c.*2009T>C rs886058236
NM_003722.5(TP63):c.*2197C>A rs886058237
NM_003722.5(TP63):c.*2205A>G rs886058238
NM_003722.5(TP63):c.*221G>A rs886058224
NM_003722.5(TP63):c.*2273A>G rs886058239
NM_003722.5(TP63):c.*235_*238del rs886058225
NM_003722.5(TP63):c.*2426C>T rs568346565
NM_003722.5(TP63):c.*2555dup rs772929136
NM_003722.5(TP63):c.*295T>A rs886058226
NM_003722.5(TP63):c.*382A>G rs886058227
NM_003722.5(TP63):c.*519C>T rs886058228
NM_003722.5(TP63):c.1374A>G (p.Ser458=) rs141794685
NM_003722.5(TP63):c.1644C>T (p.Ser548=) rs763019843
NM_003722.5(TP63):c.1994T>G (p.Met665Arg) rs886058223
NM_003722.5(TP63):c.409G>C (p.Asp137His) rs762935508
NM_003722.5(TP63):c.63-1G>C rs200607940
NM_003722.5(TP63):c.766+3A>G rs886058221
NM_003722.5(TP63):c.766+5G>A rs374425727
NM_003722.5(TP63):c.899C>A (p.Thr300Lys) rs886058222

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