ClinVar Miner

List of variants reported as likely pathogenic for Nasopharyngeal Neoplasms

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Total variants: 27
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HGVS dbSNP
NM_000141.4(FGFR2):c.1642A>C (p.Ile548Leu) rs1057519901
NM_000141.4(FGFR2):c.1645A>C (p.Asn549His) rs1057519045
NM_000141.4(FGFR2):c.1647T>A (p.Asn549Lys) rs121913476
NM_000546.5(TP53):c.523C>G (p.Arg175Gly) rs138729528
NM_000546.5(TP53):c.523C>T (p.Arg175Cys) rs138729528
NM_000546.5(TP53):c.638G>A (p.Arg213Gln) rs587778720
NM_000546.5(TP53):c.638G>C (p.Arg213Pro) rs587778720
NM_000546.5(TP53):c.838A>G (p.Arg280Gly) rs753660142
NM_000546.5(TP53):c.839G>A (p.Arg280Lys) rs121912660
NM_000546.5(TP53):c.839G>C (p.Arg280Thr) rs121912660
NM_001126112.2(TP53):c.637C>G (p.Arg213Gly) rs397516436
NM_001126114.2(TP53):c.638G>T (p.Arg213Leu) rs587778720
NM_001126115.1(TP53):c.443G>T (p.Arg148Ile) rs121912660
NM_002524.3(NRAS):c.182A>C (p.Gln61Pro) rs11554290
NM_002524.3(NRAS):c.182A>G (p.Gln61Arg) rs11554290
NM_002524.3(NRAS):c.183A>T (p.Gln61His) rs121913255
NM_002524.4(NRAS):c.181C>A (p.Gln61Lys) rs121913254
NM_002524.4(NRAS):c.182A>T (p.Gln61Leu) rs11554290
NM_005343.2(HRAS):c.34G>T (p.Gly12Cys) rs104894229
NM_005343.2(HRAS):c.35G>C (p.Gly12Ala) rs104894230
NM_006218.3(PIK3CA):c.1633G>C (p.Glu545Gln) rs104886003
NM_006218.3(PIK3CA):c.1634A>C (p.Glu545Ala) rs121913274
NM_006218.3(PIK3CA):c.1634A>G (p.Glu545Gly) rs121913274
NM_006218.3(PIK3CA):c.1635G>T (p.Glu545Asp) rs121913275
NM_006218.4(PIK3CA):c.1633G>A (p.Glu545Lys) rs104886003
NM_022970.3(FGFR2):c.1917T>A (p.Asn639Lys) rs1057519854
NM_176795.4(HRAS):c.34G>A (p.Gly12Ser) rs104894229

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