ClinVar for Gene (Select 126807510) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2655704	NM_015082.2(FSTL4):c.1374C>T (p.Ser458=)	FSTL4, LOC126807510	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2513876	NM_015082.2(FSTL4):c.1423C>T (p.His475Tyr)	FSTL4, LOC126807510 (H475Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370425	NM_015082.2(FSTL4):c.1378G>A (p.Asp460Asn)	FSTL4, LOC126807510 (D460N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 775075	NM_015082.2(FSTL4):c.1375G>A (p.Asp459Asn)	FSTL4, LOC126807510 (D459N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 149858	GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3	LOC129995052, LOC129995053 +1157 more	Copy number gain	See cases	GPathogenic
Select item 146119	GRCh38/hg38 5q31.1(chr5:131626503-135815054)x1	LOC129994691, LOC129994692 +263 more	Copy number loss	See cases	GPathogenic
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 58360	GRCh38/hg38 5q31.1(chr5:132816203-135383158)x1	AFF4, AFF4-DT +147 more	Copy number loss	See cases	GPathogenic
Select item 57483	GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3	ABLIM3, ACSL6 +1218 more	Copy number gain	See cases	GPathogenic

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