Apod Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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22 records found for search term Apod

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578536	CV112920	single nucleotide variant	NM_001647.3(APOD):c.334+239G>C	Lung cancer [RCV000093443]	uncertain significance	3	195571038	195571038	Human		name
8578537	CV112921	single nucleotide variant	NM_001647.3(APOD):c.124-2165C>G	Lung cancer [RCV000093444]	uncertain significance	3	195576136	195576136	Human		name
8578538	CV112922	single nucleotide variant	NM_001647.3(APOD):c.-34-1226G>T	Lung cancer [RCV000093445]	uncertain significance	3	195580721	195580721	Human		name
15160322	CV748156	single nucleotide variant	NM_001647.4(APOD):c.165C>A (p.Thr55=)	not provided [RCV000925461]	likely benign	3	195573930	195573930	Human		name
156221084	CV2222453	single nucleotide variant	NM_001647.4(APOD):c.31C>G (p.Leu11Val)	not specified [RCV004099307]	uncertain significance	3	195579431	195579431	Human		name
156004161	CV2357537	single nucleotide variant	NM_001647.4(APOD):c.85C>T (p.Pro29Ser)	not specified [RCV004202811]	uncertain significance	3	195579377	195579377	Human		name
405662624	CV3289885	single nucleotide variant	NM_001647.4(APOD):c.74T>C (p.Leu25Pro)	not specified [RCV004417830]	uncertain significance	3	195579388	195579388	Human		name
15165765	CV697996	single nucleotide variant	NM_001647.4(APOD):c.44T>C (p.Phe15Ser)	APOD-related disorder [RCV003895753]\|not provided [RCV000948671]	benign	3	195579418	195579418	Human	2	name , trait , alternate_id
15165765	CV697996	single nucleotide variant	NM_001647.4(APOD):c.44T>C (p.Phe15Ser)	APOD-related disorder [RCV003895753]\|not provided [RCV000948671]	benign	3	195579418	195579419	Human	2	name , trait , alternate_id
155914221	CV2341950	single nucleotide variant	NM_001647.4(APOD):c.142G>A (p.Glu48Lys)	not specified [RCV004184894]	uncertain significance	3	195573953	195573953	Human		name
401781026	CV2681866	single nucleotide variant	NM_001647.4(APOD):c.178C>T (p.Arg60Cys)	not specified [RCV004296860]	uncertain significance	3	195573917	195573917	Human		name
401927656	CV2825150	single nucleotide variant	NM_001647.4(APOD):c.226G>A (p.Val76Met)	not provided [RCV003439098]	benign	3	195573869	195573869	Human		name
405258464	CV3203829	single nucleotide variant	NM_001647.4(APOD):c.166T>G (p.Phe56Val)	APOD-related disorder [RCV003941998]	benign	3	195573929	195573929	Human		name , trait , alternate_id
405662619	CV3289883	single nucleotide variant	NM_001647.4(APOD):c.160A>C (p.Thr54Pro)	not specified [RCV004417828]	uncertain significance	3	195573935	195573935	Human		name
405662622	CV3289884	single nucleotide variant	NM_001647.4(APOD):c.274G>C (p.Gly92Arg)	not specified [RCV004417829]	uncertain significance	3	195571337	195571337	Human		name
597678037	CV3572405	single nucleotide variant	NM_001647.4(APOD):c.157C>T (p.Pro53Ser)	not specified [RCV004837059]	uncertain significance	3	195573938	195573938	Human		name
155982943	CV2347843	single nucleotide variant	NM_001647.4(APOD):c.559A>G (p.Lys187Glu)	not specified [RCV004195495]	likely benign	3	195568911	195568911	Human		name
156339472	CV2351587	single nucleotide variant	NM_001647.4(APOD):c.304C>G (p.Pro102Ala)	not specified [RCV004195306]	uncertain significance	3	195571307	195571307	Human		name
156221103	CV2397413	single nucleotide variant	NM_001647.4(APOD):c.370G>A (p.Asp124Asn)	not specified [RCV004238932]	uncertain significance	3	195569100	195569100	Human		name
329374113	CV2443658	single nucleotide variant	NM_001647.4(APOD):c.350C>T (p.Pro117Leu)	not specified [RCV004255963]	uncertain significance	3	195569120	195569120	Human		name
405283650	CV3191782	single nucleotide variant	NM_001647.4(APOD):c.383A>G (p.Tyr128Cys)	APOD-related disorder [RCV003921882]	likely benign	3	195569087	195569087	Human		name , trait , alternate_id
597677935	CV3572395	single nucleotide variant	NM_001647.4(APOD):c.531G>A (p.Met177Ile)	not specified [RCV004837049]	uncertain significance	3	195568939	195568939	Human		name

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