ClinVar Miner

List of variants in gene RBFOX1 reported as benign

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_018723.4(RBFOX1):c.-64+166491C>A rs7187508 0.62707
NM_018723.4(RBFOX1):c.931-19A>G rs2302213 0.10758
NM_018723.4(RBFOX1):c.126G>A (p.Thr42=) rs17143930 0.03708
NM_018723.4(RBFOX1):c.137C>A (p.Pro46His) rs113298071 0.00341
NM_018723.4(RBFOX1):c.96C>G (p.Pro32=) rs143695164 0.00052
NM_018723.4(RBFOX1):c.270+10C>G rs113881725 0.00051
NM_018723.4(RBFOX1):c.264C>T (p.Thr88=) rs202136920 0.00038
NM_018723.4(RBFOX1):c.144C>T (p.Pro48=) rs61742359 0.00027
NM_018723.4(RBFOX1):c.70C>T (p.Pro24Ser) rs148751394 0.00026
NM_145893.3(RBFOX1):c.57G>A (p.Pro19=) rs147261087 0.00016
NM_018723.4(RBFOX1):c.708G>A (p.Glu236=) rs368113568 0.00009
GRCh37/hg19 16p13.3(chr16:6218884-6817375)x1
GRCh37/hg19 16p13.3(chr16:6296764-6394153)x1
GRCh37/hg19 16p13.3(chr16:6350982-6382434)x1
GRCh37/hg19 16p13.3(chr16:6352110-6382434)x1
GRCh37/hg19 16p13.3(chr16:6380696-6435694)x1
GRCh37/hg19 16p13.3(chr16:6382434-6432358)x1
GRCh37/hg19 16p13.3(chr16:6575078-6679243)x1
GRCh37/hg19 16p13.3(chr16:6637943-6660833)x1
GRCh37/hg19 16p13.3(chr16:6772948-6785659)x1
GRCh37/hg19 16p13.3(chr16:6980832-7038142)x1
GRCh37/hg19 16p13.3(chr16:7046160-7073977)x1
GRCh37/hg19 16p13.3(chr16:7062553-7082045)x1
GRCh37/hg19 16p13.3(chr16:7103790-7129095)x1
GRCh37/hg19 16p13.3(chr16:7105253-7125380)x1
GRCh37/hg19 16p13.3(chr16:7105253-7129095)x1
GRCh37/hg19 16p13.3(chr16:7115290-7178540)x1
GRCh37/hg19 16p13.3(chr16:7155989-7167354)x1
GRCh37/hg19 16p13.3(chr16:7212889-7239022)x1
GRCh37/hg19 16p13.3(chr16:7753601-7890984)x1
GRCh38/hg38 16p13.3(chr16:6253203-6552025)x1
GRCh38/hg38 16p13.3(chr16:6900958-6922247)x1
NM_018723.4(RBFOX1):c.-126-6_-126-4del rs200320825
NM_018723.4(RBFOX1):c.28-11del
NM_018723.4(RBFOX1):c.28-7847G>C
NM_018723.4(RBFOX1):c.758-4G>T rs112339093
NM_018723.4(RBFOX1):c.758-5C>T rs368263619
NM_018723.4(RBFOX1):c.879G>A (p.Pro293=) rs200006523
NM_018723.4(RBFOX1):c.879G>C (p.Pro293=) rs200006523

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