Osr1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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30 records found for search term Osr1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15139234	CV774647	single nucleotide variant	NM_145260.3(OSR1):c.666-6C>T	not provided [RCV000943521]	likely benign	2	19352416	19352416	Human		name
8576900	CV111269	single nucleotide variant	NM_145260.2(OSR1):c.665+252C>T	Lung cancer [RCV000091792]	uncertain significance	2	19352889	19352889	Human		name
150455639	CV1220489	single nucleotide variant	NM_145260.3(OSR1):c.666-218A>G	not provided [RCV001612582]	benign	2	19352628	19352628	Human		name
401866355	CV2762617	single nucleotide variant	NM_145260.3(OSR1):c.4G>A (p.Gly2Ser)	not specified [RCV004340184]	uncertain significance	2	19353802	19353802	Human		name
150448509	CV1214986	single nucleotide variant	NM_145260.3(OSR1):c.654G>A (p.Leu218=)	not provided [RCV001611575]	benign	2	19353152	19353152	Human		name
401776365	CV2703205	single nucleotide variant	NM_145260.3(OSR1):c.94A>G (p.Thr32Ala)	not specified [RCV004315576]	uncertain significance	2	19353712	19353712	Human		name
401929363	CV2815559	single nucleotide variant	NM_145260.3(OSR1):c.456C>T (p.Asp152=)	not provided [RCV003407168]	likely benign	2	19353350	19353350	Human		name
405785443	CV3374341	single nucleotide variant	NM_145260.3(OSR1):c.37C>T (p.His13Tyr)	not specified [RCV004504554]	uncertain significance	2	19353769	19353769	Human		name
405784507	CV3374342	single nucleotide variant	NM_145260.3(OSR1):c.74A>C (p.Gln25Pro)	not specified [RCV004504555]	uncertain significance	2	19353732	19353732	Human		name
407511417	CV3459722	single nucleotide variant	NM_145260.3(OSR1):c.29T>C (p.Val10Ala)	not specified [RCV004648041]	uncertain significance	2	19353777	19353777	Human		name
597656078	CV3567796	single nucleotide variant	NM_145260.3(OSR1):c.60C>G (p.Asn20Lys)	not specified [RCV004827471]	uncertain significance	2	19353746	19353746	Human		name
597736204	CV3567798	single nucleotide variant	NM_145260.3(OSR1):c.97G>A (p.Val33Met)	not specified [RCV004843692]	uncertain significance	2	19353709	19353709	Human		name
15131643	CV733038	single nucleotide variant	NM_145260.3(OSR1):c.345G>T (p.Pro115=)	not provided [RCV000897810]	benign\|likely benign	2	19353461	19353461	Human		name
15195575	CV762752	single nucleotide variant	NM_145260.3(OSR1):c.429T>C (p.Pro143=)	not provided [RCV000933974]	likely benign	2	19353377	19353377	Human		name
15098792	CV762753	single nucleotide variant	NM_145260.3(OSR1):c.417C>T (p.Gly139=)	not provided [RCV000936357]	likely benign	2	19353389	19353389	Human		name
156139710	CV2212111	single nucleotide variant	NM_145260.3(OSR1):c.286A>C (p.Ile96Leu)	not specified [RCV004089015]	uncertain significance	2	19353520	19353520	Human		name
156135740	CV2245629	single nucleotide variant	NM_145260.3(OSR1):c.263C>A (p.Ala88Asp)	not specified [RCV004111519]	uncertain significance	2	19353543	19353543	Human		name
156214036	CV2257432	single nucleotide variant	NM_145260.3(OSR1):c.181G>A (p.Ala61Thr)	not specified [RCV004125511]	uncertain significance	2	19353625	19353625	Human		name
156060585	CV2263063	single nucleotide variant	NM_145260.3(OSR1):c.127G>A (p.Gly43Ser)	not specified [RCV004131318]	uncertain significance	2	19353679	19353679	Human		name
329357084	CV2457531	single nucleotide variant	NM_145260.3(OSR1):c.209C>T (p.Ser70Phe)	not specified [RCV004267340]	uncertain significance	2	19353597	19353597	Human		name
329394425	CV2469865	single nucleotide variant	NM_145260.3(OSR1):c.101C>T (p.Pro34Leu)	not specified [RCV004285341]	uncertain significance	2	19353705	19353705	Human		name
405784496	CV3374340	single nucleotide variant	NM_145260.3(OSR1):c.167C>T (p.Thr56Met)	not specified [RCV004504553]	uncertain significance	2	19353639	19353639	Human		name
597736193	CV3567794	single nucleotide variant	NM_145260.3(OSR1):c.194C>T (p.Pro65Leu)	not specified [RCV004843690]	uncertain significance	2	19353612	19353612	Human		name
597736198	CV3567797	single nucleotide variant	NM_145260.3(OSR1):c.179C>A (p.Pro60Gln)	not specified [RCV004843691]	uncertain significance	2	19353627	19353627	Human		name
156308983	CV2366513	single nucleotide variant	NM_145260.3(OSR1):c.752C>T (p.Thr251Met)	not specified [RCV004208488]	uncertain significance	2	19352324	19352324	Human		name
156225416	CV2390599	single nucleotide variant	NM_145260.3(OSR1):c.569T>G (p.Leu190Arg)	not specified [RCV004239125]	uncertain significance	2	19353237	19353237	Human		name
329379422	CV2443403	single nucleotide variant	NM_145260.3(OSR1):c.457G>A (p.Val153Met)	not specified [RCV004262246]	uncertain significance	2	19353349	19353349	Human		name
401889805	CV2763406	single nucleotide variant	NM_145260.3(OSR1):c.446C>A (p.Ala149Asp)	not specified [RCV004349295]	uncertain significance	2	19353360	19353360	Human		name
401887198	CV2773226	single nucleotide variant	NM_145260.3(OSR1):c.425C>T (p.Ser142Phe)	not specified [RCV004353907]	uncertain significance	2	19353381	19353381	Human		name
407511413	CV3459721	single nucleotide variant	NM_145260.3(OSR1):c.321C>A (p.Ser107Arg)	not specified [RCV004648040]	uncertain significance	2	19353485	19353485	Human		name

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