Qk Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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13 records found for search term Qk

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8581702	CV116147	single nucleotide variant	NM_006775.2(QKI):c.*8160G>C	Lung cancer [RCV000096670]	uncertain significance	6	163578870	163578870	Human		name
150479985	CV1258345	deletion	NM_006775.3(QKI):c.286-6del	not provided [RCV001685764]	benign	6	163478763	163478763	Human		name
150532253	CV1294692	single nucleotide variant	NM_006775.3(QKI):c.142+9C>T	not provided [RCV001752184]	benign	6	163415344	163415344	Human		name
407459898	CV3496944	single nucleotide variant	NM_006775.3(QKI):c.634+2T>C	not provided [RCV004698759]	not provided	6	163562071	163562071	Human		name
156165868	CV2200854	single nucleotide variant	NM_006775.3(QKI):c.353G>C (p.Gly118Ala)	not specified [RCV004081482]	uncertain significance	6	163478847	163478847	Human		name
156009023	CV2294296	single nucleotide variant	NM_006775.3(QKI):c.694C>T (p.Pro232Ser)	not specified [RCV004151426]	uncertain significance	6	163563479	163563479	Human		name
156171540	CV2400690	single nucleotide variant	NM_006775.3(QKI):c.625A>G (p.Ile209Val)	not specified [RCV004242366]	uncertain significance	6	163562060	163562060	Human		name
401750160	CV2715526	single nucleotide variant	NM_006775.3(QKI):c.956G>A (p.Arg319Gln)	not specified [RCV004326927]	uncertain significance	6	163566742	163566742	Human		name
407473995	CV3464967	single nucleotide variant	NM_006775.3(QKI):c.718G>T (p.Ala240Ser)	not specified [RCV004662887]	uncertain significance	6	163563503	163563503	Human		name
597774067	CV3592622	single nucleotide variant	NM_006775.3(QKI):c.751A>G (p.Ile251Val)	not specified [RCV004851885]	uncertain significance	6	163563536	163563536	Human		name
597774072	CV3592623	single nucleotide variant	NM_006775.3(QKI):c.730C>T (p.Pro244Ser)	not specified [RCV004851886]	uncertain significance	6	163563515	163563515	Human		name
598252447	CV3898301	single nucleotide variant	NM_006775.3(QKI):c.725G>A (p.Arg242His)	not specified [RCV005259426]	uncertain significance	6	163563510	163563510	Human		name
405668286	CV3308248	single nucleotide variant	NM_006775.3(QKI):c.1013C>G (p.Ala338Gly)	not specified [RCV004440720]	uncertain significance	6	163570697	163570697	Human		name