C1863534[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 108

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 347962	NM_006017.3(PROM1):c.*1160A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 901959	NM_006017.3(PROM1):c.*1149A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 902864	NM_006017.3(PROM1):c.*1143A>C	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347963	NM_006017.3(PROM1):c.*1078A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GBenign
Select item 347964	NM_006017.3(PROM1):c.*1070A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347965	NM_006017.3(PROM1):c.*1052G>A	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GConflicting classifications of pathogenicity
Select item 901462	NM_006017.3(PROM1):c.*985C>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347966	NM_006017.3(PROM1):c.*963A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 900368	NM_006017.3(PROM1):c.*781G>A	PROM1	Single nucleotide variant (3 prime UTR variant)	Cone-rod dystrophy 12 +3 more	GUncertain significance
Select item 347967	NM_006017.3(PROM1):c.*684C>T	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GConflicting classifications of pathogenicity
Select item 900369	NM_006017.3(PROM1):c.*681C>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Cone-rod dystrophy 12 +3 more	GUncertain significance
Select item 347968	NM_006017.3(PROM1):c.*667A>C	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +4 more	GBenign
Select item 901516	NM_006017.3(PROM1):c.*640T>A	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 902098	NM_006017.3(PROM1):c.*580T>A	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347969	NM_006017.3(PROM1):c.*551A>T	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 902975	NM_006017.3(PROM1):c.*198T>C	PROM1	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 900420	NM_006017.3(PROM1):c.*189A>G	PROM1	Single nucleotide variant (3 prime UTR variant)	Cone-rod dystrophy 12 +3 more	GUncertain significance
Select item 900421	NM_006017.3(PROM1):c.*107G>T	PROM1	Single nucleotide variant (3 prime UTR variant)	Cone-rod dystrophy 12 +3 more	GUncertain significance
Select item 900422	NM_006017.3(PROM1):c.2582+9A>C	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 347971	NM_006017.3(PROM1):c.2578A>G (p.Thr860Ala)	PROM1 (T860A +1 more)	Single nucleotide variant (missense variant +1 more)	Cone-rod dystrophy 12 +4 more	GConflicting classifications of pathogenicity
Select item 347972	NM_006017.3(PROM1):c.2551G>A (p.Val851Ile)	PROM1 (V851I +1 more)	Single nucleotide variant (missense variant +1 more)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 347973	NM_006017.3(PROM1):c.2508G>A (p.Met836Ile)	PROM1 (M836I +1 more)	Single nucleotide variant (missense variant +1 more)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 902154	NM_006017.3(PROM1):c.2489+8T>C	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 903034	NM_006017.3(PROM1):c.2485G>A (p.Asp829Asn)	PROM1 (D820N +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +5 more	GConflicting classifications of pathogenicity
Select item 347974	NM_006017.3(PROM1):c.2480T>C (p.Val827Ala)	PROM1 (V827A +1 more)	Single nucleotide variant (missense variant)	Retinal macular dystrophy type 2 +4 more	GUncertain significance
Select item 899417	NM_006017.3(PROM1):c.2397A>G (p.Gly799=)	PROM1	Single nucleotide variant (synonymous variant)	Cone-rod dystrophy 12 +3 more	GUncertain significance
Select item 95334	NM_006017.3(PROM1):c.2374-6T>C	PROM1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign
Select item 347976	NM_006017.3(PROM1):c.2373+13C>G	PROM1	Single nucleotide variant (intron variant)	Stargardt disease 4 +3 more	GUncertain significance
Select item 347977	NM_006017.3(PROM1):c.2364C>T (p.Ile788=)	PROM1	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 347978	NM_006017.3(PROM1):c.2309C>A (p.Pro770His)	PROM1 (P770H +1 more)	Single nucleotide variant (missense variant)	Cone-rod dystrophy 12 +5 more	GConflicting classifications of pathogenicity
Select item 347979	NM_006017.3(PROM1):c.2284A>G (p.Ser762Gly)	PROM1 (S762G +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 347980	NM_006017.3(PROM1):c.2281-5C>G	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +4 more	GUncertain significance
Select item 95330	NM_006017.3(PROM1):c.2281-6C>G	PROM1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign
Select item 289616	NM_006017.3(PROM1):c.2271C>T (p.Ile757=)	PROM1	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 347981	NM_006017.3(PROM1):c.2211+7C>T	PROM1	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 684463	NM_006017.3(PROM1):c.2112C>T (p.Arg704=)	PROM1	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 900895	NM_006017.3(PROM1):c.2094C>A (p.Ser698Arg)	PROM1 (S689R +1 more)	Single nucleotide variant (missense variant)	Cone-rod dystrophy 12 +4 more	GConflicting classifications of pathogenicity
Select item 902565	NM_006017.3(PROM1):c.2050C>G (p.Arg684Gly)	PROM1 (R675G +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 259905	NM_006017.3(PROM1):c.1983+14G>A	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +5 more	GBenign
Select item 347982	NM_006017.3(PROM1):c.1982T>C (p.Leu661Ser)	PROM1 (L661S +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 95329	NM_006017.3(PROM1):c.1977C>T (p.Asn659=)	PROM1	Single nucleotide variant (synonymous variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 347983	NM_006017.3(PROM1):c.1954T>G (p.Tyr652Asp)	PROM1 (Y652D +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 287074	NM_006017.3(PROM1):c.1928C>G (p.Ala643Gly)	PROM1 (A643G +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 347984	NM_006017.3(PROM1):c.1911+14G>A	PROM1	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 636187	NM_006017.3(PROM1):c.1911+8G>A	PROM1	Single nucleotide variant (intron variant)	Stargardt disease 4 +4 more	GConflicting classifications of pathogenicity
Select item 347985	NM_006017.3(PROM1):c.1871G>A (p.Cys624Tyr)	PROM1 (C624Y +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 100578	NM_006017.3(PROM1):c.1768-5C>T	PROM1	Single nucleotide variant (intron variant)	not specified +5 more	GBenign/Likely benign
Select item 787025	NM_006017.3(PROM1):c.1751A>G (p.His584Arg)	PROM1 (H584R +1 more)	Single nucleotide variant (missense variant)	PROM1-related condition +5 more	GConflicting classifications of pathogenicity
Select item 899856	NM_006017.3(PROM1):c.1738A>C (p.Asn580His)	PROM1 (N571H +1 more)	Single nucleotide variant (missense variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 347986	NM_006017.3(PROM1):c.1717C>T (p.Leu573Phe)	PROM1 (L573F +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 899857	NM_006017.3(PROM1):c.1710C>T (p.Tyr570=)	PROM1	Single nucleotide variant (synonymous variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 347987	NM_006017.3(PROM1):c.1683-3C>T	PROM1	Single nucleotide variant (intron variant)	Stargardt disease 4 +4 more	GConflicting classifications of pathogenicity
Select item 347988	NM_006017.3(PROM1):c.1579-6T>C	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 901585	NM_006017.3(PROM1):c.1579-12A>C	PROM1	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 347989	NM_006017.3(PROM1):c.1578+9G>C	PROM1	Single nucleotide variant (intron variant)	Cone-rod dystrophy 12 +4 more	GConflicting classifications of pathogenicity
Select item 347990	NM_006017.3(PROM1):c.1576C>T (p.Arg526Trp)	PROM1 (R526W +1 more)	Single nucleotide variant (missense variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 167535	NM_006017.3(PROM1):c.1497C>T (p.Ile499=)	PROM1	Single nucleotide variant (synonymous variant)	Stargardt disease 4 +5 more	GConflicting classifications of pathogenicity
Select item 347991	NM_006017.3(PROM1):c.1491G>T (p.Leu497Phe)	PROM1 (L497F +1 more)	Single nucleotide variant (missense variant)	Retinal macular dystrophy type 2 +4 more	GConflicting classifications of pathogenicity
Select item 899918	NM_006017.3(PROM1):c.1468A>T (p.Ser490Cys)	PROM1 (S481C +1 more)	Single nucleotide variant (missense variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 901090	NM_006017.3(PROM1):c.1407G>A (p.Pro469=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 901091	NM_006017.3(PROM1):c.1387T>C (p.Tyr463His)	PROM1 (Y454H +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347992	NM_006017.3(PROM1):c.1377C>T (p.Gly459=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 194072	NM_006017.3(PROM1):c.1345G>A (p.Val449Met)	PROM1 (V449M +1 more)	Single nucleotide variant (missense variant)	PROM1-related condition +5 more	GConflicting classifications of pathogenicity
Select item 347993	NM_006017.3(PROM1):c.1344C>T (p.Ile448=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 899993	NM_006017.3(PROM1):c.1301+11C>A	PROM1	Single nucleotide variant (intron variant)	Cone-rod dystrophy 12 +3 more	GConflicting classifications of pathogenicity
Select item 899994	NM_006017.3(PROM1):c.1301+10T>A	PROM1	Single nucleotide variant (intron variant)	Cone-rod dystrophy 12 +3 more	GConflicting classifications of pathogenicity
Select item 757831	NM_006017.3(PROM1):c.1279T>C (p.Leu427=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 347994	NM_006017.3(PROM1):c.1279T>A (p.Leu427Met)	PROM1 (L427M +1 more)	Single nucleotide variant (missense variant)	Stargardt disease 4 +4 more	GUncertain significance
Select item 347995	NM_006017.3(PROM1):c.1271T>C (p.Leu424Ser)	PROM1 (L424S +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347996	NM_006017.3(PROM1):c.1218C>G (p.Leu406=)	PROM1	Single nucleotide variant (synonymous variant)	Cone-rod dystrophy 12 +4 more	GConflicting classifications of pathogenicity
Select item 391392	NM_006017.3(PROM1):c.1199T>C (p.Leu400Pro)	PROM1 (L400P +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 903654	NM_006017.3(PROM1):c.1195C>T (p.Arg399Cys)	PROM1 (R390C +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +4 more	GConflicting classifications of pathogenicity
Select item 842166	NM_006017.3(PROM1):c.1152G>C (p.Arg384Ser)	PROM1 (R375S +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 864624	NM_006017.3(PROM1):c.1036A>G (p.Asn346Asp)	PROM1 (N337D +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +4 more	GUncertain significance
Select item 438212	NM_006017.3(PROM1):c.1002+5G>A	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 347997	NM_006017.3(PROM1):c.963G>T (p.Leu321Phe)	PROM1 (L321F +1 more)	Single nucleotide variant (missense variant)	Cone-rod dystrophy 12 +6 more	GConflicting classifications of pathogenicity
Select item 289314	NM_006017.3(PROM1):c.868A>C (p.Ser290Arg)	PROM1 (S290R +1 more)	Single nucleotide variant (missense variant)	Retinal dystrophy +7 more	GConflicting classifications of pathogenicity
Select item 347998	NM_006017.3(PROM1):c.843C>T (p.His281=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 347999	NM_006017.3(PROM1):c.792G>A (p.Lys264=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 259907	NM_006017.3(PROM1):c.786G>A (p.Ala262=)	PROM1	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +6 more	GBenign
Select item 348001	NM_006017.3(PROM1):c.731G>A (p.Arg244Gln)	PROM1 (R244Q +1 more)	Single nucleotide variant (missense variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 348002	NM_006017.3(PROM1):c.718G>A (p.Gly240Arg)	PROM1 (G240R +1 more)	Single nucleotide variant (missense variant)	Stargardt disease 4 +4 more	GUncertain significance
Select item 348003	NM_006017.3(PROM1):c.717C>T (p.Gly239=)	PROM1	Single nucleotide variant (synonymous variant)	Stargardt disease 4 +4 more	GConflicting classifications of pathogenicity
Select item 717840	NM_006017.3(PROM1):c.714A>G (p.Gly238=)	PROM1	Single nucleotide variant (synonymous variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 901286	NM_006017.3(PROM1):c.706G>A (p.Val236Met)	PROM1 (V227M +1 more)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 348004	NM_006017.3(PROM1):c.678G>A (p.Ala226=)	PROM1	Single nucleotide variant (synonymous variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 809628	NM_006017.3(PROM1):c.677C>T (p.Ala226Val)	PROM1 (A226V +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 348005	NM_006017.3(PROM1):c.631-14T>C	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +5 more	GBenign/Likely benign
Select item 191189	NM_006017.3(PROM1):c.604C>G (p.Arg202Gly)	PROM1 (R202G +1 more)	Single nucleotide variant (missense variant)	Cone-rod dystrophy 12 +5 more	GConflicting classifications of pathogenicity
Select item 348006	NM_006017.3(PROM1):c.556C>T (p.Arg186Trp)	PROM1 (R186W +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 900186	NM_006017.3(PROM1):c.380G>T (p.Gly127Val)	PROM1 (G127V +1 more)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 901350	NM_006017.3(PROM1):c.376G>A (p.Val126Met)	PROM1 (V117M +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 259906	NM_006017.3(PROM1):c.303+6G>A	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +6 more	GBenign
Select item 348007	NM_006017.3(PROM1):c.277-15C>T	PROM1	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 348008	NM_006017.3(PROM1):c.276+15G>T	PROM1	Single nucleotide variant (intron variant)	Retinitis pigmentosa +3 more	GConflicting classifications of pathogenicity
Select item 902806	NM_006017.3(PROM1):c.250T>A (p.Tyr84Asn)	PROM1 (Y84N)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GUncertain significance
Select item 95331	NM_006017.3(PROM1):c.228G>A (p.Leu76=)	PROM1	Single nucleotide variant (synonymous variant)	Retinal dystrophy +6 more	GBenign
Select item 348009	NM_006017.3(PROM1):c.181A>G (p.Ile61Val)	PROM1 (I61V)	Single nucleotide variant (missense variant)	Stargardt disease 4 +4 more	GConflicting classifications of pathogenicity
Select item 900247	NM_006017.3(PROM1):c.158G>A (p.Gly53Asp)	PROM1 (G53D)	Single nucleotide variant (missense variant)	Retinal dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 348010	NM_006017.3(PROM1):c.155T>C (p.Ile52Thr)	PROM1 (I52T)	Single nucleotide variant (missense variant)	Cone-rod dystrophy 12 +4 more	GUncertain significance

<< First< Prev

Page of 2