List of variants in gene TFAP2A reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001372066.1(TFAP2A):c.826T>C (p.Leu276=)	rs35008125	0.00674
NM_001372066.1(TFAP2A):c.426C>T (p.Leu142=)	rs369051842	0.00067
NM_001372066.1(TFAP2A):c.924C>T (p.Tyr308=)	rs141711078	0.00046
NM_001372066.1(TFAP2A):c.141G>A (p.Leu47=)	rs149126243	0.00039
NM_001372066.1(TFAP2A):c.257C>T (p.Pro86Leu)	rs200131527	0.00018
NM_001372066.1(TFAP2A):c.1215C>T (p.Thr405=)	rs201494266	0.00008
NM_001372066.1(TFAP2A):c.51+20G>T	rs369679945	0.00006
NM_001372066.1(TFAP2A):c.474C>G (p.Ile158Met)	rs1295010353	0.00005
NM_001372066.1(TFAP2A):c.103A>G (p.Thr35Ala)	rs9368354	0.00002
NM_001372066.1(TFAP2A):c.860A>G (p.Asn287Ser)	rs1021266565

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