"GeneDx"[submitter] AND "DDX25"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59772	GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	AASDHPPT, ABCG4 +1199 more	Copy number gain	See cases	GPathogenic
Select item 59777	GRCh38/hg38 11q23.3-25(chr11:120236432-135040246)x3	OR8G5, PANX3 +519 more	Copy number gain	See cases	GPathogenic
Select item 1266919	NM_001330438.2(DDX25):c.-280+632G>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295373	NM_001330438.2(DDX25):c.-280+726C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274522	NM_001330438.2(DDX25):c.-280+761G>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250886	NM_001330438.2(DDX25):c.-280+872_-280+890del	DDX25	Microsatellite (intron variant)	not provided	GBenign
Select item 1227047	NM_013264.5(DDX25):c.311+155G>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258301	NM_013264.5(DDX25):c.311+263C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277621	NM_013264.5(DDX25):c.312-141G>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251045	NM_013264.5(DDX25):c.404+36T>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182265	NM_013264.5(DDX25):c.507+53T>A	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268446	NM_013264.5(DDX25):c.507+55G>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246498	NM_013264.5(DDX25):c.508-343G>A	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268031	NM_013264.5(DDX25):c.508-154A>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182717	NM_013264.5(DDX25):c.508-65C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248283	NM_013264.5(DDX25):c.804T>G (p.Ala268=)	DDX25	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1174372	NM_013264.5(DDX25):c.1038+297C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236347	NM_013264.5(DDX25):c.1038+315G>A	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295363	NM_013264.5(DDX25):c.1038+333A>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179392	NM_013264.5(DDX25):c.1039-268C>A	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222364	NM_013264.5(DDX25):c.1194T>C (p.Cys398=)	DDX25	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1236363	NM_013264.5(DDX25):c.1201+300G>A	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279289	NM_013264.5(DDX25):c.1202-271AC[12]	DDX25	Microsatellite (intron variant)	not provided	GBenign
Select item 1225308	NM_013264.5(DDX25):c.1202-271AC[15]	DDX25	Microsatellite (intron variant)	not provided	GBenign
Select item 1235858	NM_013264.5(DDX25):c.1202-69C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272526	NM_013264.5(DDX25):c.1390+242C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239112	NM_013264.5(DDX25):c.1391-299T>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247045	NM_013264.5(DDX25):c.*280T>G	DDX25	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 253601	GRCh37/hg19 11q23.3-25(chr11:119807473-134868407)x1	ACAD8, ACRV1 +113 more	Copy number loss	See cases	GPathogenic
Select item 253521	GRCh37/hg19 11q23.3-25(chr11:120615374-134868407)x1	CCDC15, CDON +108 more	Copy number loss	See cases	GPathogenic

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Items: 30