Ubn1 Variant Search Result - Rat Genome Database

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16 records found for search term Ubn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15119383	CV779845	single nucleotide variant	NM_001079514.3(UBN1):c.1431-4G>A	not provided [RCV000962540]	benign	16	4870840	4870840	Human		name
15111182	CV726656	single nucleotide variant	NM_001079514.3(UBN1):c.378C>T (p.Ile126=)	not provided [RCV000894220]	likely benign	16	4858609	4858609	Human		name
15118471	CV714934	single nucleotide variant	NM_001079514.3(UBN1):c.1923C>T (p.Leu641=)	not provided [RCV000962386]	benign	16	4874333	4874333	Human		name
15135642	CV714935	single nucleotide variant	NM_001079514.3(UBN1):c.2673A>C (p.Ser891=)	not provided [RCV000965321]	benign	16	4875083	4875083	Human		name
15163106	CV726657	single nucleotide variant	NM_001079514.3(UBN1):c.2016G>A (p.Ser672=)	not provided [RCV000881896]	benign	16	4874426	4874426	Human		name
15170604	CV755202	single nucleotide variant	NM_001079514.3(UBN1):c.1569G>C (p.Leu523=)	not provided [RCV000927734]	likely benign	16	4871164	4871164	Human		name
15187865	CV770914	single nucleotide variant	NM_001079514.3(UBN1):c.2574A>G (p.Ala858=)	not provided [RCV000931784]	likely benign	16	4874984	4874984	Human		name
8627826	CV82970	single nucleotide variant	NM_001079514.2(UBN1):c.2823C>A (p.Ser941=)	Malignant melanoma [RCV000063050]	not provided	16	4875233	4875233	Human		name
401938502	CV2811042	single nucleotide variant	NM_001079514.3(UBN1):c.3111C>T (p.Ala1037=)	not provided [RCV003417623]	likely benign	16	4876957	4876957	Human		name
15187880	CV703709	single nucleotide variant	NM_001079514.3(UBN1):c.868C>G (p.Leu290Val)	not provided [RCV000953718]	benign	16	4860860	4860860	Human		name
15200571	CV703711	single nucleotide variant	NM_001079514.3(UBN1):c.3342G>A (p.Pro1114=)	not provided [RCV000957369]	benign	16	4877461	4877461	Human		name
15111046	CV714936	single nucleotide variant	NM_001079514.3(UBN1):c.3237C>T (p.Pro1079=)	not provided [RCV000961026]	benign	16	4877083	4877083	Human		name
10044834	CV188282	single nucleotide variant	NM_001079514.3(UBN1):c.2356T>A (p.Leu786Met)	Non-immune hydrops fetalis [RCV000170572]	likely pathogenic	16	4874766	4874766	Human	2	name
15161442	CV703710	single nucleotide variant	NM_001079514.3(UBN1):c.2494G>C (p.Ala832Pro)	not provided [RCV000947674]	benign	16	4874904	4874904	Human		name
15151743	CV740207	single nucleotide variant	NM_001079514.3(UBN1):c.1869G>C (p.Leu623Phe)	not provided [RCV000901425]	benign	16	4874279	4874279	Human		name
8627825	CV82969	single nucleotide variant	NM_001079514.2(UBN1):c.2822C>T (p.Ser941Phe)	Malignant melanoma [RCV000063049]	not provided	16	4875232	4875232	Human		name