C3887898[trait identifier] AND "National Health Commission Key Laborat - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809802	NM_001164664.2(MAST4):c.2693T>C (p.Ile898Thr)	MAST4 (I692T +5 more)	Single nucleotide variant (missense variant)	Infantile spasms	GLikely pathogenic
Select item 1809803	NM_001164664.2(MAST4):c.4412C>T (p.Thr1471Ile)	MAST4 (T1203I +8 more)	Single nucleotide variant (missense variant)	Infantile spasms	GUncertain significance
Select item 1809804	NM_001164664.2(MAST4):c.7655C>G (p.Ser2552Trp)	MAST4 (S2284W +8 more)	Single nucleotide variant (missense variant)	Infantile spasms	GLikely pathogenic

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ClinVar