Hnrnpf Variant Search Result - Rat Genome Database

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16 records found for search term Hnrnpf

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405791263	CV3266974	single nucleotide variant	NM_001098204.2(HNRNPF):c.45C>T (p.Leu15=)	not specified [RCV004399797]	likely benign	10	43387840	43387840	Human		name
405791258	CV3266972	single nucleotide variant	NM_001098204.2(HNRNPF):c.10G>T (p.Gly4Cys)	not specified [RCV004399795]	uncertain significance	10	43387875	43387875	Human		name
405791260	CV3266973	single nucleotide variant	NM_001098204.2(HNRNPF):c.23G>T (p.Gly8Val)	not specified [RCV004399796]	uncertain significance	10	43387862	43387862	Human		name
407527874	CV3433718	single nucleotide variant	NM_001098204.2(HNRNPF):c.199G>A (p.Val67Ile)	not specified [RCV004632935]	uncertain significance	10	43387686	43387686	Human		name
155265272	CV1695485	single nucleotide variant	NM_001098204.2(HNRNPF):c.635G>C (p.Arg212Pro)	not provided [RCV002280217]	uncertain significance	10	43387250	43387250	Human		name
156052836	CV2312388	single nucleotide variant	NM_001098204.2(HNRNPF):c.658A>G (p.Ile220Val)	not specified [RCV004167082]	uncertain significance	10	43387227	43387227	Human		name
329390642	CV2459309	single nucleotide variant	NM_001098204.2(HNRNPF):c.719A>G (p.Tyr240Cys)	not specified [RCV004274729]	uncertain significance	10	43387166	43387166	Human		name
401866673	CV2472796	single nucleotide variant	NM_001098204.2(HNRNPF):c.781G>A (p.Gly261Arg)	not provided [RCV003331493]	uncertain significance	10	43387104	43387104	Human		name
405791266	CV3266975	single nucleotide variant	NM_001098204.2(HNRNPF):c.813G>T (p.Met271Ile)	not specified [RCV004399798]	uncertain significance	10	43387072	43387072	Human		name
407527870	CV3433716	single nucleotide variant	NM_001098204.2(HNRNPF):c.832G>A (p.Asp278Asn)	not specified [RCV004632934]	uncertain significance	10	43387053	43387053	Human		name
407510762	CV3433717	single nucleotide variant	NM_001098204.2(HNRNPF):c.955A>G (p.Ile319Val)	not specified [RCV004626230]	uncertain significance	10	43386930	43386930	Human		name
597791580	CV3679446	single nucleotide variant	NM_001098204.2(HNRNPF):c.387G>T (p.Gln129His)	not specified [RCV004933579]	uncertain significance	10	43387498	43387498	Human		name
598190884	CV3975484	single nucleotide variant	NM_001098204.2(HNRNPF):c.433G>A (p.Val145Met)	not specified [RCV005354199]	uncertain significance	10	43387452	43387452	Human		name
156043066	CV2305766	single nucleotide variant	NM_001098204.2(HNRNPF):c.1106A>G (p.Asn369Ser)	not specified [RCV004167574]	uncertain significance	10	43386779	43386779	Human		name
401719171	CV2704991	single nucleotide variant	NM_001098204.2(HNRNPF):c.1240T>G (p.Tyr414Asp)	not specified [RCV004309596]	uncertain significance	10	43386645	43386645	Human		name
598190892	CV3975485	single nucleotide variant	NM_001098204.2(HNRNPF):c.1112C>T (p.Ala371Val)	not specified [RCV005354200]	uncertain significance	10	43386773	43386773	Human		name