C1866070[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 898330	NM_003352.8(SUMO1):c.*1038C>T	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 333609	NM_003352.8(SUMO1):c.*944G>C	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 333610	NM_003352.8(SUMO1):c.*884A>G	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 895351	NM_003352.8(SUMO1):c.*814G>A	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 895352	NM_003352.8(SUMO1):c.*776A>T	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 895353	NM_003352.8(SUMO1):c.*753C>G	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 333611	NM_003352.8(SUMO1):c.*724A>G	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 333612	NM_003352.8(SUMO1):c.*545G>T	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 333613	NM_003352.8(SUMO1):c.*475A>G	SUMO1	Single nucleotide variant (3 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 895354	NM_003352.8(SUMO1):c.88-8C>T	SUMO1	Single nucleotide variant (intron variant)	Orofacial cleft 10	GUncertain significance
Select item 333615	NM_003352.8(SUMO1):c.-32T>G	SUMO1	Single nucleotide variant (5 prime UTR variant +1 more)	Orofacial cleft 10	GLikely benign
Select item 896763	NM_003352.8(SUMO1):c.-48C>T	SUMO1	Single nucleotide variant (5 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 896764	NM_003352.8(SUMO1):c.-83A>G	SUMO1	Single nucleotide variant (5 prime UTR variant +1 more)	Orofacial cleft 10	GUncertain significance
Select item 896765	NM_003352.8(SUMO1):c.-94G>A	SUMO1	Single nucleotide variant (5 prime UTR variant +1 more)	Orofacial cleft 10	GLikely benign