C2675859[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1602324	NM_000996.4(RPL35A):c.11+17T>C	IQCG, RPL35A	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 5	GLikely benign
Select item 344528	NM_000996.4(RPL35A):c.21C>T (p.Ser7=)	IQCG, RPL35A	Single nucleotide variant (synonymous variant +1 more)	Diamond-Blackfan anemia +3 more	GBenign/Likely benign
Select item 942903	NM_000996.4(RPL35A):c.34G>A (p.Ala12Thr)	IQCG, RPL35A (A12T)	Single nucleotide variant (missense variant +1 more)	Diamond-Blackfan anemia 5	GUncertain significance
Select item 1169618	NM_000996.4(RPL35A):c.282T>C (p.Ala94=)	IQCG, RPL35A	Single nucleotide variant (synonymous variant +1 more)	Diamond-Blackfan anemia 5 +1 more	GBenign/Likely benign
Select item 572707	NM_000996.4(RPL35A):c.309+4A>T	IQCG, RPL35A	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 5	GUncertain significance

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