Prss35 Variant Search Result - Rat Genome Database

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35 records found for search term Prss35

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15158101	CV735790	single nucleotide variant	NM_153362.3(PRSS35):c.192C>A (p.Ile64=)	not provided [RCV000902666]	benign	6	83523633	83523633	Human		name
156072936	CV2233405	single nucleotide variant	NM_153362.3(PRSS35):c.34A>G (p.Thr12Ala)	not specified [RCV004105763]	uncertain significance	6	83523475	83523475	Human		name
329402640	CV2451133	single nucleotide variant	NM_153362.3(PRSS35):c.82A>T (p.Met28Leu)	not specified [RCV004270067]	uncertain significance	6	83523523	83523523	Human		name
15108061	CV722156	single nucleotide variant	NM_153362.3(PRSS35):c.825T>C (p.Tyr275=)	not provided [RCV000893598]	benign	6	83524266	83524266	Human		name
156330570	CV2224286	single nucleotide variant	NM_153362.3(PRSS35):c.140G>A (p.Ser47Asn)	not specified [RCV004096107]	uncertain significance	6	83523581	83523581	Human		name
156097122	CV2399166	single nucleotide variant	NM_153362.3(PRSS35):c.104C>G (p.Pro35Arg)	not specified [RCV004246597]	uncertain significance	6	83523545	83523545	Human		name
401717698	CV2703968	single nucleotide variant	NM_153362.3(PRSS35):c.200A>G (p.Gln67Arg)	not specified [RCV004308864]	uncertain significance	6	83523641	83523641	Human		name
401876624	CV2767656	single nucleotide variant	NM_153362.3(PRSS35):c.100G>T (p.Val34Leu)	not specified [RCV004345796]	uncertain significance	6	83523541	83523541	Human		name
405654483	CV3379299	single nucleotide variant	NM_153362.3(PRSS35):c.118G>C (p.Glu40Gln)	not specified [RCV004510669]	uncertain significance	6	83523559	83523559	Human		name
405654485	CV3379300	single nucleotide variant	NM_153362.3(PRSS35):c.123G>T (p.Arg41Ser)	not specified [RCV004510670]	uncertain significance	6	83523564	83523564	Human		name
405654488	CV3379301	single nucleotide variant	NM_153362.3(PRSS35):c.193G>A (p.Glu65Lys)	not specified [RCV004510671]	uncertain significance	6	83523634	83523634	Human		name
15145476	CV710625	single nucleotide variant	NM_153362.3(PRSS35):c.1014C>T (p.Tyr338=)	not provided [RCV000967004]	benign	6	83524455	83524455	Human		name
15170715	CV735791	single nucleotide variant	NM_153362.3(PRSS35):c.1176T>C (p.Thr392=)	not provided [RCV000905320]	likely benign	6	83524617	83524617	Human		name
156147288	CV2196945	single nucleotide variant	NM_153362.3(PRSS35):c.500C>T (p.Ala167Val)	not specified [RCV004071403]	uncertain significance	6	83523941	83523941	Human		name
329396418	CV2462654	single nucleotide variant	NM_153362.3(PRSS35):c.753G>C (p.Trp251Cys)	not specified [RCV004278591]	uncertain significance	6	83524194	83524194	Human		name
401760419	CV2709844	single nucleotide variant	NM_153362.3(PRSS35):c.431T>A (p.Phe144Tyr)	not specified [RCV004320817]	uncertain significance	6	83523872	83523872	Human		name
405654490	CV3379302	single nucleotide variant	NM_153362.3(PRSS35):c.628G>A (p.Ala210Thr)	not specified [RCV004510672]	likely benign	6	83524069	83524069	Human		name
405654493	CV3379303	single nucleotide variant	NM_153362.3(PRSS35):c.758G>A (p.Arg253Gln)	not specified [RCV004510673]	uncertain significance	6	83524199	83524199	Human		name
405654495	CV3379304	single nucleotide variant	NM_153362.3(PRSS35):c.961G>T (p.Val321Phe)	not specified [RCV004510674]	uncertain significance	6	83524402	83524402	Human		name
407514055	CV3461550	single nucleotide variant	NM_153362.3(PRSS35):c.850C>T (p.Arg284Cys)	not specified [RCV004649045]	uncertain significance	6	83524291	83524291	Human		name
597771538	CV3581565	single nucleotide variant	NM_153362.3(PRSS35):c.675G>C (p.Glu225Asp)	not specified [RCV004851359]	likely benign	6	83524116	83524116	Human		name
597771543	CV3581566	single nucleotide variant	NM_153362.3(PRSS35):c.935T>A (p.Phe312Tyr)	not specified [RCV004851360]	uncertain significance	6	83524376	83524376	Human		name
597771548	CV3581567	single nucleotide variant	NM_153362.3(PRSS35):c.653G>A (p.Gly218Asp)	not specified [RCV004851361]	uncertain significance	6	83524094	83524094	Human		name
597771553	CV3581568	single nucleotide variant	NM_153362.3(PRSS35):c.484C>A (p.Gln162Lys)	not specified [RCV004851362]	uncertain significance	6	83523925	83523925	Human		name
597771558	CV3581569	single nucleotide variant	NM_153362.3(PRSS35):c.680C>A (p.Ala227Glu)	not specified [RCV004851363]	uncertain significance	6	83524121	83524121	Human		name
597771563	CV3581570	single nucleotide variant	NM_153362.3(PRSS35):c.790G>T (p.Ala264Ser)	not specified [RCV004851364]	uncertain significance	6	83524231	83524231	Human		name
598161105	CV3897827	single nucleotide variant	NM_153362.3(PRSS35):c.814A>C (p.Thr272Pro)	not specified [RCV005261168]	uncertain significance	6	83524255	83524255	Human		name
598161100	CV3897828	single nucleotide variant	NM_153362.3(PRSS35):c.464G>A (p.Ser155Asn)	not specified [RCV005261169]	uncertain significance	6	83523905	83523905	Human		name
598160609	CV3897829	single nucleotide variant	NM_153362.3(PRSS35):c.617G>C (p.Ser206Thr)	not specified [RCV005261170]	uncertain significance	6	83524058	83524058	Human		name
8632182	CV87388	single nucleotide variant	NM_001170423.1(PRSS35):c.234G>A (p.Leu78=)	Malignant melanoma [RCV000067479]	not provided	6	83523675	83523675	Human		name
156176429	CV2374446	single nucleotide variant	NM_153362.3(PRSS35):c.1231G>T (p.Ala411Ser)	not specified [RCV004231955]	uncertain significance	6	83524672	83524672	Human		name
405654480	CV3379298	single nucleotide variant	NM_153362.3(PRSS35):c.1099A>G (p.Ile367Val)	not specified [RCV004510668]	uncertain significance	6	83524540	83524540	Human		name
8632183	CV87389	single nucleotide variant	NM_001170423.1(PRSS35):c.235G>A (p.Glu79Lys)	Malignant melanoma [RCV000067480]	not provided	6	83523676	83523676	Human		name
8632184	CV87390	single nucleotide variant	NM_001170423.1(PRSS35):c.1002C>T (p.Leu334=)	Malignant melanoma [RCV000067481]	not provided	6	83524443	83524443	Human		name
8632185	CV87391	single nucleotide variant	NM_001170423.1(PRSS35):c.1018G>A (p.Asp340Asn)	Malignant melanoma [RCV000067482]	not provided	6	83524459	83524459	Human		name

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