DNAL4[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 57629	GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1	ANKRD54, APOL1 +293 more	Copy number loss	See cases	GPathogenic
Select item 57942	GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3	LOC130067651, LOC130067652 +1004 more	Copy number gain	See cases	GPathogenic
Select item 153362	GRCh38/hg38 22q13.1(chr22:37447222-39103680)x1	ANKRD54, APOBEC3A +177 more	Copy number loss	See cases	GPathogenic
Select item 57632	GRCh38/hg38 22q13.1(chr22:37721777-38886664)x1	ANKRD54, BAIAP2L2 +122 more	Copy number loss	See cases	GPathogenic
Select item 57943	GRCh38/hg38 22q13.1-13.2(chr22:37721797-40860953)x3	LOC130067459, LOC130067460 +273 more	Copy number gain	See cases	GPathogenic
Select item 60013	GRCh38/hg38 22q13.1(chr22:38696778-38898386)x1	CBX6, DNAL4 +20 more	Copy number loss	See cases	GUncertain significance
Select item 3046532	NM_005740.3(DNAL4):c.279C>T (p.Phe93=)	DNAL4	Single nucleotide variant (synonymous variant)	DNAL4-related disorder	GLikely benign
Select item 2250178	NM_005740.3(DNAL4):c.275A>T (p.Tyr92Phe)	DNAL4 (Y92F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273141	NM_005740.3(DNAL4):c.211G>A (p.Val71Met)	DNAL4 (V71M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489049	NM_005740.3(DNAL4):c.166A>G (p.Met56Val)	DNAL4 (M56V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157500	NM_005740.3(DNAL4):c.153+2T>C	DNAL4	Single nucleotide variant (splice donor variant)	Mirror movements 3	GPathogenic
Select item 2508773	NM_005740.3(DNAL4):c.91A>G (p.Met31Val)	DNAL4 (M31V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386702	NM_005740.3(DNAL4):c.90G>C (p.Glu30Asp)	DNAL4 (E30D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309489	NM_005740.3(DNAL4):c.44G>A (p.Arg15Gln)	DNAL4 (R15Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 402791	NM_005740.3(DNAL4):c.36T>C (p.Asp12=)	DNAL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3062450	GRCh37/hg19 22q13.1-13.31(chr22:39044105-45794212)x3	A4GALT, ACO2 +106 more	Copy number gain	not specified	GPathogenic
Select item 2685676	GRCh37/hg19 22q13.1(chr22:39040762-39271911)x1	CBX6, CBY1 +7 more	Copy number loss	not provided	GUncertain significance
Select item 2423540	NC_000022.10:g.(?_38097373)_(39306081_?)del	ANKRD54, BAIAP2L2 +29 more	Deletion	not provided	GPathogenic
Select item 2422150	NC_000022.10:g.(?_35776672)_(42486826_?)dup	ACO2, ADSL +132 more	Duplication	Adenylosuccinate lyase deficiency	GUncertain significance
Select item 983188	GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 816479	GRCh37/hg19 22q13.1(chr22:38431917-39392250)x1	NPTXR, FAM227A +20 more	Copy number loss	See cases	GLikely pathogenic
Select item 816216	GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3	CERK, CHADL +271 more	Copy number gain	not provided	GPathogenic
Select item 685636	GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	TUBA8, TUBGCP6 +435 more	Copy number gain	not provided	GPathogenic
Select item 638097	GRCh37/hg19 22q13.1(chr22:38838246-39260032)x1	CBY1, DDX17 +10 more	Copy number loss	See cases	GUncertain significance
Select item 443342	GRCh37/hg19 22q12.3-13.1(chr22:35674826-39466442)x3	ANKRD54, APOBEC3A +76 more	Copy number gain	See cases	GLikely pathogenic
Select item 441654	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)	ANKRD54, AP1B1 +435 more	Copy number gain	See cases	GPathogenic
Select item 441653	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3	NEFH, NF2 +435 more	Copy number gain	See cases	GPathogenic
Select item 395140	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3	ZNF280A, ZNF280B +438 more	Copy number gain	See cases	GPathogenic
Select item 394709	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3	SMARCB1, SMC1B +438 more	Copy number gain	See cases	GPathogenic
Select item 253617	GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3	A4GALT, ACO2 +223 more	Copy number gain	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic

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Items: 33