"PreventionGenetics, part of Exact Sciences"[submitter] AND "PIAS4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053895	NM_015897.4(PIAS4):c.156T>C (p.Pro52=)	PIAS4	Single nucleotide variant (synonymous variant)	PIAS4-related disorder	GLikely benign
Select item 3048197	NM_015897.4(PIAS4):c.383A>T (p.Lys128Met)	PIAS4 (K128M)	Single nucleotide variant (missense variant)	PIAS4-related disorder	GLikely benign
Select item 3035994	NM_015897.4(PIAS4):c.435G>A (p.Leu145=)	PIAS4	Single nucleotide variant (synonymous variant)	PIAS4-related disorder	GLikely benign
Select item 2631167	NM_015897.4(PIAS4):c.776C>T (p.Thr259Ile)	PIAS4 (T259I)	Single nucleotide variant (missense variant)	PIAS4-related disorder	GUncertain significance
Select item 3029264	NM_015897.4(PIAS4):c.1164C>T (p.Ser388=)	PIAS4	Single nucleotide variant (synonymous variant)	PIAS4-related disorder	GLikely benign
Select item 3031852	NM_015897.4(PIAS4):c.1197G>A (p.Leu399=)	PIAS4	Single nucleotide variant (synonymous variant)	PIAS4-related disorder	GLikely benign
Select item 2341456	NM_015897.4(PIAS4):c.1225G>A (p.Ala409Thr)	PIAS4 (A409T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3043915	NM_015897.4(PIAS4):c.1330C>T (p.Leu444=)	PIAS4	Single nucleotide variant (synonymous variant)	PIAS4-related disorder	GLikely benign

ClinVar