List of variants in gene NFE2L2 reported as likely pathogenic for transitional cell carcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006164.5(NFE2L2):c.235G>A (p.Glu79Lys)	rs1057519922
NM_006164.5(NFE2L2):c.235G>C (p.Glu79Gln)	rs1057519922
NM_006164.5(NFE2L2):c.236A>T (p.Glu79Val)	rs1057519923
NM_006164.5(NFE2L2):c.237G>T (p.Glu79Asp)	rs1057519924
NM_006164.5(NFE2L2):c.85G>A (p.Asp29Asn)	rs1057519920
NM_006164.5(NFE2L2):c.85G>C (p.Asp29His)	rs1057519920
NM_006164.5(NFE2L2):c.85G>T (p.Asp29Tyr)	rs1057519920
NM_006164.5(NFE2L2):c.86A>G (p.Asp29Gly)	rs1057519921

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