DDX25[gene] - ClinVar - NCBI

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	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 148508	GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3	BCL9L, BLID +774 more	Copy number gain	See cases	GPathogenic
Select item 149257	GRCh38/hg38 11q23.3-25(chr11:116806268-135075271)x3	ABCG4, ACAD8 +769 more	Copy number gain	See cases	GPathogenic
Select item 144588	GRCh38/hg38 11q23.3-25(chr11:116851372-134998526)x3	ABCG4, ACAD8 +764 more	Copy number gain	See cases	GPathogenic
Select item 161071	GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	ABCG4, ACAD8 +764 more	Copy number gain	See cases	GPathogenic
Select item 33553	GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	LOC128772366, LOC128772367 +764 more	Copy number gain	See cases	GPathogenic
Select item 148379	GRCh38/hg38 11q23.3-25(chr11:116868935-135075271)x3	LOC130006864, LOC130006865 +763 more	Copy number gain	See cases	GPathogenic
Select item 150522	GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3	LOC130007002, LOC130007003 +499 more	Copy number gain	See cases	GPathogenic
Select item 57503	GRCh38/hg38 11q23.3-25(chr11:118789765-134998513)x3	ABCG4, ACAD8 +635 more	Copy number gain	See cases	GPathogenic
Select item 545140	Single allele	ABCG4, ACAD8 +608 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 150032	GRCh38/hg38 11q23.3-25(chr11:119424297-135075271)x1	LOC130006995, LOC130006996 +551 more	Copy number loss	See cases	GPathogenic
Select item 57238	GRCh38/hg38 11q23.3-25(chr11:119433909-134998513)x1	LOC121832824, LOC124625855 +549 more	Copy number loss	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 58924	GRCh38/hg38 11q23.3-25(chr11:120507265-134576266)x1	ACAD8, ACRV1 +488 more	Copy number loss	See cases	GPathogenic
Select item 149328	GRCh38/hg38 11q23.3-25(chr11:120515759-135075271)x1	ACAD8, ACRV1 +497 more	Copy number loss	See cases	GPathogenic
Select item 154016	GRCh38/hg38 11q24.1-25(chr11:121611476-135068576)x1	LOC126861375, LOC126861376 +444 more	Copy number loss	See cases	GPathogenic
Select item 150820	GRCh38/hg38 11q24.1-25(chr11:121689052-135075271)x1	ACAD8, ACRV1 +442 more	Copy number loss	See cases	GPathogenic
Select item 148952	GRCh38/hg38 11q24.1-25(chr11:121780459-135075271)x1	ACAD8, ACRV1 +440 more	Copy number loss	See cases	GPathogenic
Select item 154045	GRCh38/hg38 11q24.1-25(chr11:121806547-135068576)x1	ACAD8, ACRV1 +439 more	Copy number loss	See cases	GPathogenic
Select item 147400	GRCh38/hg38 11q24.1-24.2(chr11:122182443-125957977)x1	ACRV1, BSX +166 more	Copy number loss	See cases	GPathogenic
Select item 145308	GRCh38/hg38 11q24.1-25(chr11:123799938-134998526)x1	ACAD8, ACRV1 +368 more	Copy number loss	See cases	GPathogenic
Select item 149547	GRCh38/hg38 11q24.1-25(chr11:123963074-135075271)x1	ACAD8, ACRV1 +363 more	Copy number loss	See cases	GPathogenic
Select item 57206	GRCh38/hg38 11q24.2-25(chr11:124155723-134998513)x1	ACAD8, ACRV1 +353 more	Copy number loss	See cases	GPathogenic
Select item 145337	GRCh38/hg38 11q24.2-25(chr11:124205225-134998526)x1	ACAD8, ACRV1 +352 more	Copy number loss	See cases	GPathogenic
Select item 151164	GRCh38/hg38 11q24.2-25(chr11:124315025-134818116)x1	ACAD8, ACRV1 +343 more	Copy number loss	See cases	GPathogenic
Select item 149702	GRCh38/hg38 11q24.2-25(chr11:124940059-135075271)x1	LOC121392954, LOC121832822 +312 more	Copy number loss	See cases	GPathogenic
Select item 147420	GRCh38/hg38 11q24.2-25(chr11:125241472-134998513)x1	ACAD8, ACRV1 +299 more	Copy number loss	See cases	GPathogenic
Select item 57257	GRCh38/hg38 11q24.2-24.3(chr11:125891315-129072391)x1	ARHGAP32, CDON +116 more	Copy number loss	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 2522254	NM_013264.5(DDX25):c.11T>C (p.Leu4Ser)	DDX25 (L4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546712	NM_013264.5(DDX25):c.18G>C (p.Trp6Cys)	DDX25 (W6C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531893	NM_013264.5(DDX25):c.27C>G (p.Asp9Glu)	DDX25 (D9E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271283	NM_013264.5(DDX25):c.44G>C (p.Ser15Thr)	DDX25 (S15T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618327	NM_013264.5(DDX25):c.49C>T (p.Arg17Trp)	DDX25 (R17W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080959	NM_013264.5(DDX25):c.111T>A (p.Ser37Arg)	DDX25 (S37R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3080960	NM_013264.5(DDX25):c.137C>T (p.Ser46Phe)	DDX25 (S46F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2537360	NM_013264.5(DDX25):c.272C>G (p.Ser91Cys)	DDX25 (S91C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
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 3080961	NM_013264.5(DDX25):c.377T>C (p.Met126Thr)	DDX25 (M12T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1251045	NM_013264.5(DDX25):c.404+36T>C	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 768496	NM_013264.5(DDX25):c.414C>T (p.Asn138=)	DDX25	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2469746	NM_013264.5(DDX25):c.465G>C (p.Leu155Phe)	DDX25 (L155F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524453	NM_013264.5(DDX25):c.475A>G (p.Ser159Gly)	DDX25 (S159G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080962	NM_013264.5(DDX25):c.490T>G (p.Leu164Val)	DDX25 (L164V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255753	NM_013264.5(DDX25):c.502C>T (p.Pro168Ser)	DDX25 (P54S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 716171	NM_013264.5(DDX25):c.508-6C>T	DDX25	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3271285	NM_013264.5(DDX25):c.557T>G (p.Val186Gly)	DDX25 (V72G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272116	NM_013264.5(DDX25):c.563A>G (p.Glu188Gly)	DDX25 (E74G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278827	NM_013264.5(DDX25):c.626C>T (p.Pro209Leu)	DDX25 (P209L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080963	NM_013264.5(DDX25):c.635C>A (p.Thr212Asn)	DDX25 (T212N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602494	NM_013264.5(DDX25):c.674C>T (p.Thr225Ile)	DDX25 (T111I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480808	NM_013264.5(DDX25):c.769G>A (p.Gly257Arg)	DDX25 (G257R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275762	NM_013264.5(DDX25):c.782A>C (p.His261Pro)	DDX25 (H261P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080964	NM_013264.5(DDX25):c.797A>G (p.Gln266Arg)	DDX25 (Q152R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080965	NM_013264.5(DDX25):c.801A>G (p.Arg267=)	DDX25	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1248283	NM_013264.5(DDX25):c.804T>G (p.Ala268=)	DDX25	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2240808	NM_013264.5(DDX25):c.852C>G (p.Asp284Glu)	DDX25 (D284E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366485	NM_013264.5(DDX25):c.907C>T (p.Arg303Cys)	DDX25 (R189C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273417	NM_013264.5(DDX25):c.937C>T (p.Arg313Trp)	DDX25 (R313W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2508696	NM_013264.5(DDX25):c.1043G>A (p.Arg348His)	DDX25 (R234H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379972	NM_013264.5(DDX25):c.1062G>T (p.Leu354Phe)	DDX25 (L354F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271284	NM_013264.5(DDX25):c.1081G>T (p.Asp361Tyr)	DDX25 (D247Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596516	NM_013264.5(DDX25):c.1120G>A (p.Val374Met)	DDX25 (V374M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1328946	NM_013264.5(DDX25):c.1129C>T (p.Arg377Ter)	DDX25 (R263* +1 more)	Single nucleotide variant (nonsense)	Azoospermia	GPathogenic
Select item 2318469	NM_013264.5(DDX25):c.1130G>C (p.Arg377Pro)	DDX25 (R263P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2359933	NM_013264.5(DDX25):c.1300C>T (p.Arg434Trp)	DDX25 (R320W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485523	NM_013264.5(DDX25):c.1319A>T (p.Lys440Ile)	DDX25 (K440I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331118	NM_013264.5(DDX25):c.1324G>A (p.Gly442Ser)	DDX25 (G328S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2514916	NM_013264.5(DDX25):c.1414G>A (p.Ala472Thr)	DDX25 (A472T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1247045	NM_013264.5(DDX25):c.*280T>G	DDX25	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 3148862	GRCh37/hg19 11q23.3-25(chr11:116683755-134937416)x3	ABCG4, ACAD8 +177 more	Copy number gain	not provided	GPathogenic
Select item 3063218	GRCh37/hg19 11q24.1-25(chr11:123523103-134938470)x1	ACAD8, ACRV1 +92 more	Copy number loss	not specified	GPathogenic
Select item 3063194	GRCh37/hg19 11q24.1-25(chr11:121423232-134938470)x1	ACAD8, ACRV1 +104 more	Copy number loss	not specified	GPathogenic
Select item 3063192	GRCh37/hg19 11q24.2-25(chr11:125511834-134938470)x1	ACAD8, ACRV1 +49 more	Copy number loss	not specified	GPathogenic
Select item 3063186	GRCh37/hg19 11q23.3-24.2(chr11:121183636-127620828)x1	ACRV1, BLID +73 more	Copy number loss	not specified	GPathogenic
Select item 2671625	Single allele	AASDHPPT, ABCG4 +275 more	Duplication	not provided	GPathogenic
Select item 2506544	GRCh37/hg19 11q23.3-25(chr11:120531028-134257553)	JHY, RPUSD4 +107 more	Copy number loss	11q partial monosomy syndrome	GPathogenic
Select item 2426317	NC_000011.9:g.(?_123504851)_(126163012_?)del	ACRV1, CCDC15 +56 more	Deletion	not provided	GUncertain significance
Select item 1808652	GRCh37/hg19 11q24.1-25(chr11:122975824-134938470)x1	ACAD8, ACRV1 +94 more	Copy number loss	not provided	GPathogenic

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