List of variants in gene MAP2K1 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=)	rs148656020	0.00024
NM_002755.4(MAP2K1):c.693+20T>C	rs753107656	0.00001
NM_002755.4(MAP2K1):c.961C>T (p.Pro321Ser)	rs771613524	0.00001
NM_002755.4(MAP2K1):c.291+14_291+20delinsTCTCACCAATCACCA	rs1064795401
NM_002755.4(MAP2K1):c.323G>T (p.Arg108Leu)	rs727504819
NM_002755.4(MAP2K1):c.364A>G (p.Asn122Asp)	rs876657651
NM_002755.4(MAP2K1):c.389A>G (p.Tyr130Cys)	rs121908595

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