"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RPS26"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 309857	NM_001029.5(RPS26):c.-22C>G	RPS26	Single nucleotide variant (5 prime UTR variant)	Diamond-Blackfan anemia 10 +2 more	GBenign
Select item 309858	NM_001029.5(RPS26):c.-3A>G	RPS26	Single nucleotide variant (5 prime UTR variant)	Diamond-Blackfan anemia 10 +2 more	GBenign/Likely benign
Select item 1157119	NM_001029.5(RPS26):c.3+7C>G	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 883851	NM_001029.5(RPS26):c.3+9T>A	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10 +1 more	GLikely benign
Select item 883852	NM_001029.5(RPS26):c.3+14C>T	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 1652790	NM_001029.5(RPS26):c.3+20G>C	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 703119	NM_001029.5(RPS26):c.63T>A (p.Ile21=)	RPS26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 946046	NM_001029.5(RPS26):c.181+6_181+7del	RPS26	Deletion (intron variant)	Diamond-Blackfan anemia 10	GUncertain significance
Select item 1541909	NM_001029.5(RPS26):c.181+10T>G	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 1659857	NM_001029.5(RPS26):c.181+19C>G	RPS26	Single nucleotide variant (intron variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 1551609	NM_001029.5(RPS26):c.207G>C (p.Val69=)	RPS26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 1020612	NM_001029.5(RPS26):c.266G>A (p.Arg89His)	RPS26 (R89H)	Single nucleotide variant (missense variant)	Diamond-Blackfan anemia 10	GUncertain significance
Select item 883853	NM_001029.5(RPS26):c.291C>T (p.Pro97=)	RPS26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 10	GLikely benign
Select item 651454	NM_001029.5(RPS26):c.312G>A (p.Ala104=)	RPS26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 10	GUncertain significance
Select item 1577732	NM_001029.5(RPS26):c.315T>A (p.Gly105=)	RPS26	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia +1 more	GLikely benign