Spry1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Spry1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150512968	CV1228855	single nucleotide variant	NM_001258038.2(SPRY1):c.*77G>C	not provided [RCV001637697]	benign	4	123402628	123402628	Human		name
150482339	CV1261605	single nucleotide variant	NM_001258038.2(SPRY1):c.*32T>C	not provided [RCV001686208]	benign	4	123402583	123402583	Human		name
150547109	CV1291879	duplication	NM_001258038.2(SPRY1):c.-63dup	not specified [RCV001733556]	benign	4	123397832	123397833	Human		name
150505290	CV1286152	single nucleotide variant	NM_001258038.2(SPRY1):c.-55-59C>A	not provided [RCV001719575]	benign	4	123401478	123401478	Human		name
150505544	CV1286217	single nucleotide variant	NM_001258038.2(SPRY1):c.-55-98G>A	not provided [RCV001719642]	benign	4	123401439	123401439	Human		name
405294501	CV3211559	single nucleotide variant	NM_001258038.2(SPRY1):c.18A>G (p.Gln6=)	SPRY1-related disorder [RCV003934399]	likely benign	4	123401609	123401609	Human		name , trait , alternate_id
155953653	CV2264365	single nucleotide variant	NM_001258038.2(SPRY1):c.20A>G (p.His7Arg)	not specified [RCV004138271]	uncertain significance	4	123401611	123401611	Human		name
405270134	CV3215369	single nucleotide variant	NM_001258038.2(SPRY1):c.255G>A (p.Val85=)	SPRY1-related disorder [RCV003949127]	benign	4	123401846	123401846	Human		name , trait , alternate_id
405289200	CV3204971	single nucleotide variant	NM_001258038.2(SPRY1):c.495C>T (p.Asp165=)	SPRY1-related disorder [RCV003961603]	likely benign	4	123402086	123402086	Human		name , trait , alternate_id
405287331	CV3210637	single nucleotide variant	NM_001258038.2(SPRY1):c.86A>G (p.Tyr29Cys)	SPRY1-related disorder [RCV003924408]	likely benign	4	123401677	123401677	Human		name , trait , alternate_id
597679730	CV3604000	single nucleotide variant	NM_001258038.2(SPRY1):c.97A>G (p.Ile33Val)	not specified [RCV004857313]	uncertain significance	4	123401688	123401688	Human		name
598272561	CV3915623	single nucleotide variant	NM_001258038.2(SPRY1):c.70C>T (p.Arg24Cys)	not specified [RCV005282657]	uncertain significance	4	123401661	123401661	Human		name
156139671	CV2246897	single nucleotide variant	NM_001258038.2(SPRY1):c.143G>A (p.Arg48Lys)	not specified [RCV004112699]	uncertain significance	4	123401734	123401734	Human		name
156262164	CV2282457	single nucleotide variant	NM_001258038.2(SPRY1):c.242T>C (p.Ile81Thr)	not specified [RCV004133263]	uncertain significance	4	123401833	123401833	Human		name
156146653	CV2311103	single nucleotide variant	NM_001258038.2(SPRY1):c.173C>G (p.Ser58Trp)	not specified [RCV004164099]	uncertain significance	4	123401764	123401764	Human		name
156038232	CV2332613	single nucleotide variant	NM_001258038.2(SPRY1):c.226A>G (p.Arg76Gly)	not specified [RCV004189294]	uncertain significance	4	123401817	123401817	Human		name
329379553	CV2443456	single nucleotide variant	NM_001258038.2(SPRY1):c.206C>T (p.Pro69Leu)	not specified [RCV004262293]	uncertain significance	4	123401797	123401797	Human		name
401743157	CV2694068	single nucleotide variant	NM_001258038.2(SPRY1):c.197G>A (p.Arg66Gln)	not specified [RCV004302503]	uncertain significance	4	123401788	123401788	Human		name
405276573	CV3206787	single nucleotide variant	NM_001258038.2(SPRY1):c.109G>A (p.Ala37Thr)	SPRY1-related disorder [RCV003917216]	likely benign	4	123401700	123401700	Human		name , trait , alternate_id
405738306	CV3333889	single nucleotide variant	NM_001258038.2(SPRY1):c.150C>G (p.Ser50Arg)	not specified [RCV004465289]	uncertain significance	4	123401741	123401741	Human		name
405738311	CV3333890	single nucleotide variant	NM_001258038.2(SPRY1):c.197G>T (p.Arg66Leu)	not specified [RCV004465290]	uncertain significance	4	123401788	123401788	Human		name
405740360	CV3333891	single nucleotide variant	NM_001258038.2(SPRY1):c.205C>T (p.Pro69Ser)	not specified [RCV004465291]	uncertain significance	4	123401796	123401796	Human		name
405740353	CV3333892	single nucleotide variant	NM_001258038.2(SPRY1):c.266A>G (p.Tyr89Cys)	not specified [RCV004465292]	uncertain significance	4	123401857	123401857	Human		name
407525746	CV3478021	single nucleotide variant	NM_001258038.2(SPRY1):c.135G>C (p.Lys45Asn)	not specified [RCV004679408]	uncertain significance	4	123401726	123401726	Human		name
407516063	CV3478022	single nucleotide variant	NM_001258038.2(SPRY1):c.154G>C (p.Glu52Gln)	not specified [RCV004675164]	uncertain significance	4	123401745	123401745	Human		name
156272463	CV2195316	single nucleotide variant	NM_001258038.2(SPRY1):c.617G>A (p.Arg206Gln)	not specified [RCV004080239]	uncertain significance	4	123402208	123402208	Human		name
155922770	CV2219136	single nucleotide variant	NM_001258038.2(SPRY1):c.838C>G (p.Leu280Val)	not specified [RCV004087292]	uncertain significance	4	123402429	123402429	Human		name
156149212	CV2265336	single nucleotide variant	NM_001258038.2(SPRY1):c.530A>C (p.His177Pro)	not specified [RCV004128226]	uncertain significance	4	123402121	123402121	Human		name
156101948	CV2291434	single nucleotide variant	NM_001258038.2(SPRY1):c.762C>G (p.Cys254Trp)	not specified [RCV004155763]	uncertain significance	4	123402353	123402353	Human		name
156006163	CV2394128	single nucleotide variant	NM_001258038.2(SPRY1):c.823C>T (p.Pro275Ser)	not specified [RCV004236330]	uncertain significance	4	123402414	123402414	Human		name
155932582	CV2400053	single nucleotide variant	NM_001258038.2(SPRY1):c.463C>T (p.Arg155Trp)	not specified [RCV004246969]	uncertain significance	4	123402054	123402054	Human		name
329368134	CV2424195	single nucleotide variant	NM_001258038.2(SPRY1):c.604T>G (p.Leu202Val)	not specified [RCV004250322]	uncertain significance	4	123402195	123402195	Human		name
329368140	CV2424197	single nucleotide variant	NM_001258038.2(SPRY1):c.764C>G (p.Ser255Cys)	not specified [RCV004250324]	uncertain significance	4	123402355	123402355	Human		name
401742148	CV2677521	single nucleotide variant	NM_001258038.2(SPRY1):c.428G>C (p.Arg143Thr)	not specified [RCV004291628]	uncertain significance	4	123402019	123402019	Human		name
401767847	CV2727298	single nucleotide variant	NM_001258038.2(SPRY1):c.548A>G (p.Gln183Arg)	not specified [RCV004327411]	uncertain significance	4	123402139	123402139	Human		name
401887838	CV2768811	single nucleotide variant	NM_001258038.2(SPRY1):c.653A>G (p.Tyr218Cys)	not specified [RCV004346938]	uncertain significance	4	123402244	123402244	Human		name
405740348	CV3333893	single nucleotide variant	NM_001258038.2(SPRY1):c.584C>T (p.Pro195Leu)	not specified [RCV004465293]	uncertain significance	4	123402175	123402175	Human		name
405740342	CV3333894	single nucleotide variant	NM_001258038.2(SPRY1):c.701A>G (p.Asn234Ser)	not specified [RCV004465294]	uncertain significance	4	123402292	123402292	Human		name
405740336	CV3333895	single nucleotide variant	NM_001258038.2(SPRY1):c.782G>T (p.Gly261Val)	not specified [RCV004465295]	uncertain significance	4	123402373	123402373	Human		name
405740327	CV3333896	single nucleotide variant	NM_001258038.2(SPRY1):c.910T>C (p.Tyr304His)	not specified [RCV004465296]	uncertain significance	4	123402501	123402501	Human		name
597679711	CV3603997	single nucleotide variant	NM_001258038.2(SPRY1):c.416C>T (p.Ser139Leu)	not specified [RCV004857311]	uncertain significance	4	123402007	123402007	Human		name
597778112	CV3603998	single nucleotide variant	NM_001258038.2(SPRY1):c.818A>C (p.Tyr273Ser)	not specified [RCV004873200]	uncertain significance	4	123402409	123402409	Human		name
597679720	CV3603999	single nucleotide variant	NM_001258038.2(SPRY1):c.493G>A (p.Asp165Asn)	not specified [RCV004857312]	uncertain significance	4	123402084	123402084	Human		name
597679737	CV3604001	single nucleotide variant	NM_001258038.2(SPRY1):c.436C>G (p.Pro146Ala)	not specified [RCV004857314]	uncertain significance	4	123402027	123402027	Human		name
597679744	CV3604002	single nucleotide variant	NM_001258038.2(SPRY1):c.878C>T (p.Pro293Leu)	not specified [RCV004857315]	uncertain significance	4	123402469	123402469	Human		name
598272545	CV3915620	single nucleotide variant	NM_001258038.2(SPRY1):c.902A>G (p.Asn301Ser)	not specified [RCV005282654]	uncertain significance	4	123402493	123402493	Human		name
598272550	CV3915621	single nucleotide variant	NM_001258038.2(SPRY1):c.836G>A (p.Cys279Tyr)	not specified [RCV005282655]	uncertain significance	4	123402427	123402427	Human		name
598272556	CV3915622	single nucleotide variant	NM_001258038.2(SPRY1):c.740C>T (p.Ser247Phe)	not specified [RCV005282656]	uncertain significance	4	123402331	123402331	Human		name
40886808	CV973415	insertion	NM_001258038.2(SPRY1):c.173_174insAG (p.Val59fs)	Inborn genetic diseases [RCV001266057]	likely pathogenic	4	123401764	123401765	Human	1	name

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