"Ambry Genetics"[submitter] AND "UBXN4"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2284131	NM_014607.4(UBXN4):c.22A>G (p.Ile8Val)	LOC107985946, LOC129934839 +1 more (I8V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2291215	NM_014607.4(UBXN4):c.177T>A (p.Asp59Glu)	UBXN4 (D59E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371134	NM_014607.4(UBXN4):c.299A>G (p.Asp100Gly)	UBXN4 (D100G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330744	NM_014607.4(UBXN4):c.321C>A (p.His107Gln)	UBXN4 (H107Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330749	NM_014607.4(UBXN4):c.329G>A (p.Arg110Gln)	UBXN4 (R110Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2338057	NM_014607.4(UBXN4):c.370G>A (p.Gly124Ser)	UBXN4 (G124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617581	NM_014607.4(UBXN4):c.448A>G (p.Arg150Gly)	UBXN4 (R150G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295020	NM_014607.4(UBXN4):c.460C>T (p.Leu154Phe)	UBXN4 (L154F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538789	NM_014607.4(UBXN4):c.499A>G (p.Thr167Ala)	UBXN4 (T167A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485647	NM_014607.4(UBXN4):c.539C>T (p.Ser180Phe)	UBXN4 (S180F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593064	NM_014607.4(UBXN4):c.722A>G (p.Lys241Arg)	UBXN4 (K241R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305953	NM_014607.4(UBXN4):c.785G>A (p.Arg262Lys)	UBXN4 (R262K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335020	NM_014607.4(UBXN4):c.823G>A (p.Asp275Asn)	UBXN4 (D275N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330745	NM_014607.4(UBXN4):c.845G>A (p.Arg282His)	UBXN4 (R282H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330747	NM_014607.4(UBXN4):c.907G>A (p.Ala303Thr)	UBXN4 (A303T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309739	NM_014607.4(UBXN4):c.943G>C (p.Glu315Gln)	UBXN4 (E315Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215156	NM_014607.4(UBXN4):c.959C>G (p.Ala320Gly)	UBXN4 (A320G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615408	NM_014607.4(UBXN4):c.1088C>T (p.Ala363Val)	UBXN4 (A363V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185918	NM_014607.4(UBXN4):c.1093A>G (p.Met365Val)	UBXN4 (M365V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220463	NM_014607.4(UBXN4):c.1108G>A (p.Glu370Lys)	UBXN4 (E370K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330746	NM_014607.4(UBXN4):c.1141C>G (p.Leu381Val)	UBXN4 (L381V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570001	NM_014607.4(UBXN4):c.1213C>T (p.His405Tyr)	UBXN4 (H405Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513174	NM_014607.4(UBXN4):c.1297T>A (p.Leu433Met)	UBXN4 (L433M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213263	NM_014607.4(UBXN4):c.1313C>T (p.Pro438Leu)	UBXN4 (P438L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271871	NM_014607.4(UBXN4):c.1376A>G (p.Lys459Arg)	UBXN4 (K459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463659	NM_014607.4(UBXN4):c.1394C>T (p.Pro465Leu)	UBXN4 (P465L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528440	NM_014607.4(UBXN4):c.1396G>A (p.Val466Met)	UBXN4 (V466M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303961	NM_014607.4(UBXN4):c.1408G>C (p.Val470Leu)	UBXN4 (V470L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185919	NM_014607.4(UBXN4):c.1429G>A (p.Asp477Asn)	UBXN4 (D477N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 29