OXNAD1[gene] - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148942	GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3	ANKRD28, ARL8B +799 more	Copy number gain	See cases	GPathogenic
Select item 148876	GRCh38/hg38 3p26.3-24.3(chr3:32241-20334387)x3	LOC129936094, LOC129936095 +647 more	Copy number gain	See cases	GPathogenic
Select item 57397	GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3	ANKRD28, ARL8B +962 more	Copy number gain	See cases	GPathogenic
Select item 153415	GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3	LOC129936377, LOC129936378 +1111 more	Copy number gain	See cases	GPathogenic
Select item 57977	GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3	LOC110120630, LOC111429626 +608 more	Copy number gain	See cases	GPathogenic
Select item 57978	GRCh38/hg38 3p25.3-22.2(chr3:11463328-38919543)x3	ACAA1, ACVR2B +730 more	Copy number gain	See cases	GPathogenic
Select item 1703229	Single allele	HDAC11, LOC126806611 +244 more	Deletion	3p- syndrome	GPathogenic
Select item 155700	GRCh38/hg38 3p25.1-24.3(chr3:14360747-21656134)x4	ANKRD28, BALR6 +214 more	Copy number gain	See cases	GPathogenic
Select item 155336	GRCh38/hg38 3p25.1-24.3(chr3:15304910-16372771)x3	ANKRD28, BTD +43 more	Copy number gain	See cases	GLikely benign
Select item 3207576	NM_138381.5(OXNAD1):c.37C>T (p.Arg13Trp)	OXNAD1 (R13W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2602413	NM_138381.5(OXNAD1):c.52G>A (p.Ala18Thr)	OXNAD1 (A36T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2253724	NM_138381.5(OXNAD1):c.71C>T (p.Ala24Val)	OXNAD1 (A42V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3207579	NM_138381.5(OXNAD1):c.83T>G (p.Leu28Trp)	OXNAD1 (L28W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2516226	NM_138381.5(OXNAD1):c.134A>G (p.Lys45Arg)	OXNAD1 (K45R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3207574	NM_138381.5(OXNAD1):c.170T>G (p.Val57Gly)	OXNAD1 (V57G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3207575	NM_138381.5(OXNAD1):c.178C>T (p.Arg60Trp)	OXNAD1 (R60W +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2353729	NM_138381.5(OXNAD1):c.184A>G (p.Ile62Val)	LOC129936290, OXNAD1 (I35V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2280523	NM_138381.5(OXNAD1):c.372A>T (p.Arg124Ser)	OXNAD1 (R142S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547053	NM_138381.5(OXNAD1):c.413C>T (p.Ala138Val)	OXNAD1 (A111V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393771	NM_138381.5(OXNAD1):c.499G>A (p.Asp167Asn)	OXNAD1 (D140N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251496	NM_138381.5(OXNAD1):c.533G>A (p.Gly178Glu)	OXNAD1 (G178E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261268	NM_138381.5(OXNAD1):c.607A>G (p.Asn203Asp)	OXNAD1 (N203D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213301	NM_138381.5(OXNAD1):c.634C>G (p.Leu212Val)	OXNAD1 (L185V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390637	NM_138381.5(OXNAD1):c.663A>T (p.Glu221Asp)	OXNAD1 (E221D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3207577	NM_138381.5(OXNAD1):c.686T>G (p.Leu229Arg)	OXNAD1 (L202R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457613	NM_138381.5(OXNAD1):c.716T>C (p.Ile239Thr)	OXNAD1 (I212T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297020	NM_138381.5(OXNAD1):c.719C>T (p.Ala240Val)	OXNAD1 (A240V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336757	NM_138381.5(OXNAD1):c.842A>G (p.Tyr281Cys)	OXNAD1 (Y254C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3207580	NM_138381.5(OXNAD1):c.844A>C (p.Ile282Leu)	OXNAD1 (I255L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255977	NM_138381.5(OXNAD1):c.898C>T (p.His300Tyr)	OXNAD1 (H300Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355897	NM_015150.2(RFTN1):c.1730A>G (p.Glu577Gly)	OXNAD1, RFTN1 (E577G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397413	NM_015150.2(RFTN1):c.1721C>T (p.Thr574Met)	OXNAD1, RFTN1 (T574M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653606	NM_015150.2(RFTN1):c.1566T>C (p.Pro522=)	OXNAD1, RFTN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2543432	NM_015150.2(RFTN1):c.1524G>A (p.Met508Ile)	OXNAD1, RFTN1 (M508I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270630	NM_015150.2(RFTN1):c.1517A>G (p.Glu506Gly)	OXNAD1, RFTN1 (E506G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591202	NM_015150.2(RFTN1):c.1459A>G (p.Lys487Glu)	OXNAD1, RFTN1 (K487E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355896	NM_015150.2(RFTN1):c.1457C>A (p.Ser486Tyr)	OXNAD1, RFTN1 (S486Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459577	NM_015150.2(RFTN1):c.1435A>G (p.Lys479Glu)	OXNAD1, RFTN1 (K479E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552992	NM_015150.2(RFTN1):c.1390G>A (p.Gly464Ser)	OXNAD1, RFTN1 (G464S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298528	NM_015150.2(RFTN1):c.1355A>G (p.Glu452Gly)	OXNAD1, RFTN1 (E452G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2560093	NM_015150.2(RFTN1):c.1352G>A (p.Arg451Lys)	OXNAD1, RFTN1 (R451K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653607	NM_015150.2(RFTN1):c.1233C>T (p.Pro411=)	OXNAD1, RFTN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3062708	GRCh37/hg19 3p26.3-22.3(chr3:61891-33946644)x3	OXTR, PDCD6IP +145 more	Copy number gain	not specified	GPathogenic
Select item 2685895	GRCh37/hg19 3p26.3-24.1(chr3:310747-28297447)x3	ANKRD28, ARL8B +121 more	Copy number gain	not provided	GPathogenic
Select item 2685071	GRCh37/hg19 3p25.1(chr3:16320205-16399521)x1	OXNAD1, RFTN1	Copy number loss	not provided	GUncertain significance
Select item 1708466	GRCh37/hg19 3p25.1-24.2(chr3:13836340-25357427)x3	ANKRD28, BTD +41 more	Copy number gain	See cases	GPathogenic
Select item 1526968	GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181)	FANCD2OS, THUMPD3 +148 more	Copy number gain	not specified	GPathogenic
Select item 1526967	GRCh37/hg19 3p26.3-24.2(chr3:61891-24432821)	ANKRD28, ARL8B +112 more	Copy number gain	not specified	GPathogenic
Select item 1340851	GRCh37/hg19 3p25.1-24.3(chr3:15085863-16402392)x3	ANKRD28, BTD +13 more	Copy number gain	not provided	GUncertain significance
Select item 688733	GRCh37/hg19 3p25.1-24.3(chr3:15752529-16524171)x3	ANKRD28, DPH3 +3 more	Copy number gain	not provided	GUncertain significance
Select item 562759	GRCh37/hg19 3p25.1(chr3:15648003-16355532)x3	ANKRD28, BTD +3 more	Copy number gain	not provided	GLikely benign
Select item 562744	GRCh37/hg19 3p26.1-24.3(chr3:5173870-16760262)x3	ANKRD28, ARL8B +84 more	Copy number gain	not provided	GPathogenic
Select item 562726	GRCh37/hg19 3p26.3-24.3(chr3:1897972-19519085)x3	ANKRD28, ARL8B +98 more	Copy number gain	not provided	GPathogenic
Select item 443469	GRCh37/hg19 3p25.1-24.3(chr3:13720222-17808236)x1	ANKRD28, BTD +27 more	Copy number loss	See cases	GLikely pathogenic
Select item 443464	GRCh37/hg19 3p26.3-22.2(chr3:61891-37459464)x3	FANCD2OS, FBLN2 +155 more	Copy number gain	See cases	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	FBXL2, FBXO40 +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 441705	GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3	ANKRD28, ARL8B +145 more	Copy number gain	See cases	GPathogenic

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Items: 58