List of variants in gene combination ESR1, SYNE1 reported by Eurofins NTD LLC (GA)

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.26209G>A (p.Gly8737Ser)	rs2295191	0.00898
NM_182961.4(SYNE1):c.26212C>T (p.Arg8738Cys)	rs144206837	0.00034
NM_182961.4(SYNE1):c.26298A>G (p.Pro8766=)	rs200880341	0.00021
NM_182961.4(SYNE1):c.26330C>G (p.Ser8777Cys)	rs377446250	0.00007
NM_182961.4(SYNE1):c.26370C>A (p.Tyr8790Ter)	rs777985131	0.00003
NM_182961.4(SYNE1):c.26173G>A (p.Asp8725Asn)	rs767663894	0.00001
NM_182961.4(SYNE1):c.26206T>G (p.Ser8736Ala)	rs886044316	0.00001
NM_182961.4(SYNE1):c.26237G>A (p.Arg8746Gln)	rs757466963	0.00001
NM_182961.4(SYNE1):c.26301G>A (p.Met8767Ile)	rs1193879156	0.00001
NM_182961.4(SYNE1):c.26345G>A (p.Arg8782Gln)	rs550697327	0.00001
NM_182961.4(SYNE1):c.26355C>T (p.His8785=)	rs771334693	0.00001
NM_182961.4(SYNE1):c.26204G>T (p.Arg8735Leu)	rs2295192
NM_182961.4(SYNE1):c.26372C>A (p.Thr8791Lys)	rs567376316
NM_182961.4(SYNE1):c.26372C>T (p.Thr8791Met)	rs567376316

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