ClinVar Miner

List of variants reported as not provided by Laboratory of Translational Genomics, National Cancer Institute

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Total variants: 42
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HGVS dbSNP
NM_000142.4(FGFR3):c.1887C>T (p.Asn629=) rs104886004
NM_000142.4(FGFR3):c.1908C>G (p.Phe636Leu) rs104886005
NM_000142.4(FGFR3):c.1935C>T (p.Leu645=) rs104886006
NM_000142.4(FGFR3):c.2129G>T (p.Gly710Val) rs104886023
NM_000142.4(FGFR3):c.2135G>A (p.Arg712His) rs104886024
NM_000546.5(TP53):c.386C>T (p.Ala129Val) rs137852792
NM_000546.5(TP53):c.414del (p.Lys139fs) rs137852794
NM_000546.5(TP53):c.448_459del (p.Thr150_Pro153del) rs137852790
NM_000546.5(TP53):c.450_459del (p.Pro151fs) rs137852791
NM_000546.5(TP53):c.460G>A (p.Gly154Ser) rs137852789
NM_000546.5(TP53):c.462C>T (p.Gly154=) rs137852793
NM_000546.5(TP53):c.666G>T (p.Pro222=) rs72661118
NM_000546.5(TP53):c.886C>T (p.His296Tyr) rs672601296
NM_000546.5(TP53):c.969G>A (p.Leu323=) rs672601297
NM_001002295.1:c.1482-5C>T
NM_001002295.2(GATA3):c.1032C>T (p.Leu344=) rs104886017
NM_001002295.2(GATA3):c.925-16C>T rs104886016
NM_004333.6(BRAF):c.1807C>T (p.Arg603Ter) rs104886015
NM_004448.3(ERBB2):c.2494-3C>T rs104886007
NM_004448.3(ERBB2):c.2506C>T (p.Leu836=) rs104886008
NM_004448.3(ERBB2):c.2520G>A (p.Arg840=) rs104886011
NM_004448.3(ERBB2):c.2535C>T (p.Asp845=) rs137852788
NM_004448.3(ERBB2):c.2568C>T (p.Pro856=) rs104886009
NM_004448.3(ERBB2):c.2605C>T (p.Leu869=) rs104886010
NM_004448.3(ERBB2):c.3146G>A (p.Ser1049Asn) rs104886025
NM_004985.5(KRAS):c.176C>T (p.Ala59Val) rs104886029
NM_004985.5(KRAS):c.216G>A (p.Met72Ile) rs104886028
NM_004985.5(KRAS):c.219G>A (p.Arg73=) rs104886027
NM_004985.5(KRAS):c.34G>A (p.Gly12Ser) rs121913530
NM_004985.5(KRAS):c.34G>T (p.Gly12Cys) rs121913530
NM_004985.5(KRAS):c.40G>A (p.Val14Ile) rs104894365
NM_005228.5(EGFR):c.2544G>A (p.Pro848=) rs104886012
NM_005228.5(EGFR):c.2602G>A (p.Glu868Lys) rs104886013
NM_005228.5(EGFR):c.2625+8G>A rs104886014
NM_005228.5(EGFR):c.2866G>A (p.Asp956Asn) rs104886026
NM_006218.2:c.1821+51A>T
NM_006218.4(PIK3CA):c.1540-56C>T rs104886002
NM_006218.4(PIK3CA):c.1571G>A (p.Arg524Lys) rs104885999
NM_006218.4(PIK3CA):c.1633G>A (p.Glu545Lys) rs104886003
NM_006218.4(PIK3CA):c.1664+18G>A rs104886001
NM_006218.4(PIK3CA):c.1664G>A (p.Arg555Lys) rs104886000
NM_006218.4(PIK3CA):c.1769G>A (p.Trp590Ter) rs104886021

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