ClinVar Miner

List of variants in gene FOXP1 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_032682.5(FOXP1):c.1146+10_1146+12delGAT rs199543140
NM_032682.5(FOXP1):c.1147-19G>A rs75214049
NM_032682.5(FOXP1):c.1240dup (p.Leu414fs) rs797044652
NM_032682.5(FOXP1):c.1317C>A (p.Tyr439Ter) rs794727155
NM_032682.5(FOXP1):c.1328A>G (p.Tyr443Cys) rs727503936
NM_032682.5(FOXP1):c.1329C>A (p.Tyr443Ter) rs1064793944
NM_032682.5(FOXP1):c.1383C>T (p.Asn461=) rs372403441
NM_032682.5(FOXP1):c.1624C>T (p.Gln542Ter) rs794727215
NM_032682.5(FOXP1):c.1652+5G>A rs794727216
NM_032682.5(FOXP1):c.1670_1685dup (p.Ser562fs) rs398124429
NM_032682.5(FOXP1):c.169C>G (p.Gln57Glu) rs752141860
NM_032682.5(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680
NM_032682.5(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845
NM_032682.5(FOXP1):c.1710_1722+2del rs1559596230
NM_032682.5(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892
NM_032682.5(FOXP1):c.1889+20C>A rs7638391
NM_032682.5(FOXP1):c.1902C>T (p.His634=) rs749771909
NM_032682.5(FOXP1):c.2020G>A (p.Glu674Lys) rs368167189
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.5(FOXP1):c.622C>T (p.Gln208Ter) rs1553709881
NM_032682.5(FOXP1):c.64G>A (p.Gly22Ser) rs794727811

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