"GeneDx"[submitter] AND "CDC14A"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146007	GRCh38/hg38 1p21.3-13.3(chr1:97272349-108893138)x1	AGL, AKNAD1 +194 more	Copy number loss	See cases	GPathogenic
Select item 60005	GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1	AGL, AHCYL1 +332 more	Copy number loss	See cases	GPathogenic
Select item 1186924	NM_001319211.2(CDC14A):c.-125-1565G>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1189779	NM_001319211.2(CDC14A):c.-125-1564C>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1197261	NM_003672.3(CDC14A):c.-470A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1234793	NM_003672.4(CDC14A):c.-333G>C	CDC14A	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1294730	NM_003672.4(CDC14A):c.-225A>T	CDC14A	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 508149	NM_003672.4(CDC14A):c.-47=	CDC14A	Single nucleotide variant (no sequence alteration +1 more)	not specified	GLikely benign
Select item 513742	NM_003672.4(CDC14A):c.-14del	CDC14A	Deletion (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 666802	NM_003672.4(CDC14A):c.28G>C (p.Gly10Arg)	CDC14A (G10R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1120113	NM_003672.4(CDC14A):c.31G>A (p.Ala11Thr)	CDC14A (A11T)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1202872	NM_003672.4(CDC14A):c.49+135A>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1278440	NM_003672.4(CDC14A):c.49+169T>G	CDC14A, LOC129931026	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 682965	NM_003672.4(CDC14A):c.50-45T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1207068	NM_003672.4(CDC14A):c.140+281C>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1212556	NM_003672.4(CDC14A):c.141-293T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1242375	NM_003672.4(CDC14A):c.141-229G>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 517571	NM_003672.4(CDC14A):c.192C>T (p.Cys64=)	CDC14A	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 1251278	NM_003672.4(CDC14A):c.217-263T>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1697125	NM_003672.4(CDC14A):c.251A>G (p.Tyr84Cys)	CDC14A (Y26C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 506035	NM_003672.4(CDC14A):c.309A>C (p.Ala103=)	CDC14A	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +1 more	GBenign
Select item 1181377	NM_003672.4(CDC14A):c.309+99C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258050	NM_003672.4(CDC14A):c.309+145A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260010	NM_003672.4(CDC14A):c.309+267A>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252574	NM_003672.4(CDC14A):c.310-18A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1712116	NM_003672.4(CDC14A):c.349G>A (p.Ala117Thr)	CDC14A (A117T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1708615	NM_003672.4(CDC14A):c.370C>G (p.Pro124Ala)	CDC14A (P124A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2571790	NM_003672.4(CDC14A):c.374C>T (p.Pro125Leu)	CDC14A (P125L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2373955	NM_003672.4(CDC14A):c.374C>A (p.Pro125His)	CDC14A (P125H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1217218	NM_003672.4(CDC14A):c.390-142G>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1196510	NM_003672.4(CDC14A):c.390-83C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1234930	NM_003672.4(CDC14A):c.456+15C>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181615	NM_003672.4(CDC14A):c.456+15C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1211692	NM_003672.4(CDC14A):c.456+111A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1217648	NM_003672.4(CDC14A):c.456+208G>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1242966	NM_003672.4(CDC14A):c.457-166A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 667084	NM_003672.4(CDC14A):c.457-6T>C	CDC14A	Single nucleotide variant (intron variant)	CDC14A-related condition +3 more	GLikely benign
Select item 1405587	NM_003672.4(CDC14A):c.512A>T (p.His171Leu)	CDC14A (H113L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1260614	NM_003672.4(CDC14A):c.519+25A>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273053	NM_003672.4(CDC14A):c.519+82T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280919	NM_003672.4(CDC14A):c.519+126G>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1285768	NM_003672.4(CDC14A):c.519+174A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1201582	NM_003672.4(CDC14A):c.520-60C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1196201	NM_003672.4(CDC14A):c.520-16T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1707252	NM_003672.4(CDC14A):c.581C>G (p.Pro194Arg)	CDC14A (P136R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 684185	NM_003672.4(CDC14A):c.607+30C>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1265286	NM_003672.4(CDC14A):c.607+142A>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1203825	NM_003672.4(CDC14A):c.607+182A>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1260334	NM_003672.4(CDC14A):c.608-152G>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 506036	NM_003672.4(CDC14A):c.608-10G>A	CDC14A	Single nucleotide variant (intron variant)	CDC14A-related condition +2 more	GBenign
Select item 1208285	NM_003672.4(CDC14A):c.717C>T (p.Asp239=)	CDC14A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1220944	NM_003672.4(CDC14A):c.778G>A (p.Val260Met)	CDC14A (V202M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1214287	NM_003672.4(CDC14A):c.780G>A (p.Val260=)	CDC14A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2507228	NM_003672.4(CDC14A):c.781C>T (p.Arg261Ter)	CDC14A (R203* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 508571	NM_003672.4(CDC14A):c.819C>G (p.Ala273=)	CDC14A	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 929950	NM_003672.4(CDC14A):c.822C>T (p.Ile274=)	CDC14A	Single nucleotide variant (synonymous variant +1 more)	CDC14A-related condition +2 more	GBenign/Likely benign
Select item 517533	NM_003672.4(CDC14A):c.825C>T (p.Ala275=)	CDC14A	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +1 more	GBenign
Select item 1218808	NM_003672.4(CDC14A):c.838+75C>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1296845	NM_003672.4(CDC14A):c.838+158C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268909	NM_003672.4(CDC14A):c.838+269C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1192712	NM_003672.4(CDC14A):c.839-124T>C	CDC14A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1186551	NM_003672.4(CDC14A):c.839-108T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 517534	NM_003672.4(CDC14A):c.903T>C (p.His301=)	CDC14A	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1712755	NM_003672.4(CDC14A):c.913A>G (p.Ile305Val)	CDC14A (I12V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1217816	NM_003672.4(CDC14A):c.957C>T (p.Pro319=)	CDC14A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 683329	NM_003672.4(CDC14A):c.977+22C>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233647	NM_003672.4(CDC14A):c.977+25C>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275146	NM_003672.4(CDC14A):c.977+62C>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1216337	NM_003672.4(CDC14A):c.977+285del	CDC14A	Deletion (intron variant)	not provided	GLikely benign
Select item 1187962	NM_003672.4(CDC14A):c.978-169T>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 508568	NM_003672.4(CDC14A):c.990G>A (p.Ser330=)	CDC14A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 235146	NM_003672.4(CDC14A):c.1015C>T (p.Arg339Ter)	CDC14A (R339* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 1201368	NM_003672.4(CDC14A):c.1033C>A (p.Arg345=)	CDC14A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 682947	NM_003672.4(CDC14A):c.1034G>A (p.Arg345Gln)	CDC14A (R287Q +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 681875	NM_003672.4(CDC14A):c.1090A>G (p.Ile364Val)	CDC14A (I364V +2 more)	Single nucleotide variant (missense variant)	CDC14A-related condition +1 more	GBenign/Likely benign
Select item 1252676	NM_003672.4(CDC14A):c.1137+188del	CDC14A	Deletion (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1235686	NM_003672.4(CDC14A):c.1138-333G>T	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1707040	NM_003672.4(CDC14A):c.1157A>T (p.Asp386Val)	CDC14A (D328V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1181232	NM_003672.4(CDC14A):c.1217G>A (p.Arg406Lys)	CDC14A (R113K +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1300914	NM_003672.4(CDC14A):c.1245A>T (p.Ala415=)	CDC14A	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1181745	NM_003672.4(CDC14A):c.1251-139A>G	CDC14A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1327802	NM_003672.4(CDC14A):c.1268G>A (p.Gly423Glu)	CDC14A (G130E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1294718	NM_003672.4(CDC14A):c.1298+188_1298+189del	CDC14A	Deletion (intron variant)	not provided	GBenign
Select item 1204283	NM_003672.4(CDC14A):c.1298+189del	CDC14A	Deletion (intron variant)	not provided	GLikely benign
Select item 1192877	NM_003672.4(CDC14A):c.1298+187_1298+189del	CDC14A	Deletion (intron variant)	not provided	GLikely benign
Select item 1280564	NM_003672.4(CDC14A):c.1298+268dup	CDC14A	Duplication (intron variant)	not provided	GBenign
Select item 1229799	NM_003672.4(CDC14A):c.1299-265T>C	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275368	NM_003672.4(CDC14A):c.1299-223T>G	CDC14A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1194190	NM_003672.4(CDC14A):c.1299-201C>A	CDC14A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1263534	NM_003672.4(CDC14A):c.1299-159_1299-158del	CDC14A	Microsatellite (intron variant)	not provided	GBenign
Select item 514410	NM_003672.4(CDC14A):c.1410C>T (p.Ala470=)	CDC14A	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1331200	NM_003672.4(CDC14A):c.1446C>T (p.Ala482=)	CDC14A	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1209164	NM_003672.4(CDC14A):c.1535C>T (p.Pro512Leu)	CDC14A (P219L +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 509180	NM_003672.4(CDC14A):c.1604A>G (p.Gln535Arg)	CDC14A (Q535R +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 517535	NM_003672.4(CDC14A):c.1647C>T (p.Ser549=)	CDC14A	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 2395825	NM_003672.4(CDC14A):c.1655G>T (p.Gly552Val)	CDC14A (G259V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 513655	NM_003672.4(CDC14A):c.1711G>A (p.Gly571Arg)	CDC14A (G571R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1211962	NM_003672.4(CDC14A):c.1730C>T (p.Ala577Val)	CDC14A (A284V +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 517536	NM_003672.4(CDC14A):c.1755+8C>T	CDC14A (A588V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign
Select item 1190616	NM_003672.4(CDC14A):c.1755+72G>A	CDC14A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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