Ugt1a5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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25 records found for search term Ugt1a5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156133207	CV2216722	single nucleotide variant	NM_019078.2(UGT1A5):c.13C>A (p.Leu5Ile)	not specified [RCV004083169]	uncertain significance	2	233713004	233713004	Human		name
401865306	CV2791601	single nucleotide variant	NM_019078.2(UGT1A5):c.23C>T (p.Pro8Leu)	not specified [RCV004358967]	uncertain significance	2	233713014	233713014	Human		name
15106120	CV708116	single nucleotide variant	NM_019078.2(UGT1A5):c.261C>T (p.Asp87=)	not provided [RCV000960014]	likely benign	2	233713252	233713252	Human		name
15169604	CV697425	single nucleotide variant	NM_019078.2(UGT1A5):c.783T>C (p.Phe261=)	not provided [RCV000949489]	benign	2	233713774	233713774	Human		name
15188855	CV719721	single nucleotide variant	NM_019078.2(UGT1A5):c.849C>T (p.Asn283=)	not provided [RCV000887657]	benign	2	233713840	233713840	Human		name
8657435	CV80440	single nucleotide variant	NM_019078.1(UGT1A5):c.459C>T (p.Pro153=)	Malignant melanoma [RCV000060517]	not provided	2	233713450	233713450	Human		name
329394283	CV2469792	single nucleotide variant	NM_019078.2(UGT1A5):c.160A>G (p.Arg54Gly)	not specified [RCV004285290]	uncertain significance	2	233713151	233713151	Human		name
13820828	CV576100	deletion	NM_019078.2(UGT1A5):c.695del (p.Ala232fs)	not provided [RCV000709907]	likely benign\|not provided	2	233713686	233713686	Human		name
8657443	CV85397	single nucleotide variant	NM_019078.2(UGT1A5):c.134G>A (p.Arg45Gln)	not specified [RCV004479506]	uncertain significance\|not provided	2	233713125	233713125	Human		name
155930465	CV2366771	single nucleotide variant	NM_019078.2(UGT1A5):c.496T>C (p.Ser166Pro)	not specified [RCV004210764]	uncertain significance	2	233713487	233713487	Human		name
401726864	CV2674578	single nucleotide variant	NM_019078.2(UGT1A5):c.520A>G (p.Arg174Gly)	not specified [RCV004291452]	uncertain significance	2	233713511	233713511	Human		name
401780690	CV2685638	single nucleotide variant	NM_019078.2(UGT1A5):c.380C>G (p.Ser127Cys)	not specified [RCV004294645]	uncertain significance	2	233713371	233713371	Human		name
401773722	CV2695342	single nucleotide variant	NM_019078.2(UGT1A5):c.720G>C (p.Gln240His)	not specified [RCV004305249]	uncertain significance	2	233713711	233713711	Human		name
401858638	CV2770577	single nucleotide variant	NM_019078.2(UGT1A5):c.773G>A (p.Arg258Gln)	not specified [RCV004349637]	uncertain significance	2	233713764	233713764	Human		name
405804984	CV3338050	single nucleotide variant	NM_019078.2(UGT1A5):c.400A>G (p.Asn134Asp)	not specified [RCV004479507]	uncertain significance	2	233713391	233713391	Human		name
597686237	CV3622942	single nucleotide variant	NM_019078.2(UGT1A5):c.443T>A (p.Val148Glu)	not specified [RCV004884152]	uncertain significance	2	233713434	233713434	Human		name
597686249	CV3622943	single nucleotide variant	NM_019078.2(UGT1A5):c.811C>A (p.Pro271Thr)	not specified [RCV004884153]	uncertain significance	2	233713802	233713802	Human		name
597719909	CV3622944	single nucleotide variant	NM_019078.2(UGT1A5):c.784G>A (p.Val262Met)	not specified [RCV004887774]	uncertain significance	2	233713775	233713775	Human		name
597686259	CV3622945	single nucleotide variant	NM_019078.2(UGT1A5):c.566A>G (p.Asn189Ser)	not specified [RCV004884154]	uncertain significance	2	233713557	233713557	Human		name
598266163	CV3929247	single nucleotide variant	NM_019078.2(UGT1A5):c.460T>G (p.Phe154Val)	not specified [RCV005301881]	likely benign	2	233713451	233713451	Human		name
598190457	CV3929248	single nucleotide variant	NM_019078.2(UGT1A5):c.463C>A (p.His155Asn)	not specified [RCV005288213]	uncertain significance	2	233713454	233713454	Human		name
598190464	CV3929249	single nucleotide variant	NM_019078.2(UGT1A5):c.511T>C (p.Phe171Leu)	not specified [RCV005288214]	uncertain significance	2	233713502	233713502	Human		name
15169589	CV697422	single nucleotide variant	NM_019078.2(UGT1A5):c.742C>A (p.Leu248Ile)	not provided [RCV000949486]	benign	2	233713733	233713733	Human	3	name
15169596	CV697423	single nucleotide variant	NM_019078.2(UGT1A5):c.745G>C (p.Val249Leu)	not provided [RCV000949487]	benign	2	233713736	233713736	Human		name
8657444	CV85398	single nucleotide variant	NM_019078.1(UGT1A5):c.572C>T (p.Ser191Phe)	Malignant melanoma [RCV000065480]	not provided	2	233713563	233713563	Human		name

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