Nkx6-3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Nkx6-3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15118197	CV779287	single nucleotide variant	NM_001364841.2(NKX6-3):c.553-7A>T	not provided [RCV000962333]	benign	8	41646701	41646701	Human		name
405707180	CV3362311	single nucleotide variant	NM_001364841.2(NKX6-3):c.553-585C>T	not specified [RCV004493299]	uncertain significance	8	41647279	41647279	Human		name
407497557	CV3458666	single nucleotide variant	NM_001364841.2(NKX6-3):c.553-619G>A	not specified [RCV004643778]	uncertain significance	8	41647313	41647313	Human		name
15118203	CV711526	single nucleotide variant	NM_001364841.2(NKX6-3):c.553-589G>T	not provided [RCV000962334]	benign	8	41647283	41647283	Human		name
155925286	CV2258501	single nucleotide variant	NM_001364841.2(NKX6-3):c.662G>C (p.Arg221Pro)	not specified [RCV004115993]	uncertain significance	8	41646585	41646585	Human		name
156179366	CV2288003	single nucleotide variant	NM_001364841.2(NKX6-3):c.607T>A (p.Ser203Thr)	not specified [RCV004147767]	uncertain significance	8	41646640	41646640	Human		name
156081771	CV2301111	single nucleotide variant	NM_001364841.2(NKX6-3):c.746G>T (p.Arg249Leu)	not specified [RCV004160031]	uncertain significance	8	41646501	41646501	Human		name
155957737	CV2304191	single nucleotide variant	NM_001364841.2(NKX6-3):c.752A>C (p.His251Pro)	not specified [RCV004170215]	uncertain significance	8	41646495	41646495	Human		name
401880649	CV2766203	single nucleotide variant	NM_001364841.2(NKX6-3):c.628C>A (p.Pro210Thr)	not specified [RCV004340645]	uncertain significance	8	41646619	41646619	Human		name
407508912	CV3458664	single nucleotide variant	NM_001364841.2(NKX6-3):c.755G>T (p.Arg252Leu)	not specified [RCV004647269]	uncertain significance	8	41646492	41646492	Human		name
407508916	CV3458665	single nucleotide variant	NM_001364841.2(NKX6-3):c.580T>C (p.Trp194Arg)	not specified [RCV004647270]	uncertain significance	8	41646667	41646667	Human		name
597651438	CV3556389	single nucleotide variant	NM_001364841.2(NKX6-3):c.778C>A (p.Leu260Met)	not specified [RCV004826887]	uncertain significance	8	41646469	41646469	Human		name
597651445	CV3556390	single nucleotide variant	NM_001364841.2(NKX6-3):c.631G>T (p.Gly211Cys)	not specified [RCV004826888]	uncertain significance	8	41646616	41646616	Human		name
597651454	CV3556391	single nucleotide variant	NM_001364841.2(NKX6-3):c.587A>G (p.Lys196Arg)	not specified [RCV004826889]	uncertain significance	8	41646660	41646660	Human		name
597651466	CV3556392	single nucleotide variant	NM_001364841.2(NKX6-3):c.692A>C (p.Tyr231Ser)	not specified [RCV004826890]	uncertain significance	8	41646555	41646555	Human		name