SCGB1C1[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151263	GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	DENND5A, DNHD1 +723 more	Copy number gain	See cases	GPathogenic
Select item 768404	NM_145651.3(SCGB1C1):c.13C>T (p.Arg5Cys)	SCGB1C1 (R5C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768405	NM_145651.3(SCGB1C1):c.66A>G (p.Thr22=)	SCGB1C1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768406	NM_145651.3(SCGB1C1):c.207T>C (p.Cys69=)	SCGB1C1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2684632	GRCh37/hg19 11p15.5-15.4(chr11:192764-3362853)x3	CARS1, CD151 +89 more	Copy number gain	not provided	GPathogenic
Select item 625559	GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136)	C11orf40, C11orf42 +243 more	Copy number gain	Silver-Russell syndrome 1	GPathogenic
Select item 394007	GRCh37/hg19 11p15.5-15.4(chr11:193187-5291338)x3	OR51G2, OR51L1 +132 more	Copy number gain	See cases	GPathogenic
Select item 393875	GRCh37/hg19 11p15.5(chr11:193842-475940)x3	ANO9, B4GALNT4 +15 more	Copy number gain	See cases	GLikely benign
Select item 253707	GRCh37/hg19 11p15.5(chr11:193142-299384)x3	RIC8A, PGGHG +7 more	Copy number gain	See cases	GUncertain significance

ClinVar