"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PRDM13" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 446239	NC_000006.12:g.99593030G>T	LOC111365204, PRDM13	Single nucleotide variant	not provided	GPathogenic
Select item 446240	NC_000006.12:g.99593111G>C	LOC111365204, PRDM13	Single nucleotide variant	not provided +1 more	GPathogenic
Select item 446241	NC_000006.12:g.99593164C>T	LOC111365204, PRDM13	Single nucleotide variant	not provided	GUncertain significance
Select item 1170404	NM_021620.4(PRDM13):c.6C>T (p.His2=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1448754	NM_021620.4(PRDM13):c.7G>C (p.Gly3Arg)	PRDM13 (G3R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1423878	NM_021620.4(PRDM13):c.13G>T (p.Ala5Ser)	PRDM13 (A5S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1357200	NM_021620.4(PRDM13):c.13G>A (p.Ala5Thr)	PRDM13 (A5T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1642853	NM_021620.4(PRDM13):c.18A>G (p.Arg6=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2075429	NM_021620.4(PRDM13):c.20C>T (p.Ala7Val)	PRDM13 (A7V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2782125	NM_021620.4(PRDM13):c.33C>A (p.Ser11Arg)	PRDM13 (S11R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1002070	NM_021620.4(PRDM13):c.55C>T (p.Pro19Ser)	PRDM13 (P19S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2096933	NM_021620.4(PRDM13):c.57G>A (p.Pro19=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1099462	NM_021620.4(PRDM13):c.57G>T (p.Pro19=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2735233	NM_021620.4(PRDM13):c.62G>T (p.Gly21Val)	PRDM13 (G21V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2702060	NM_021620.4(PRDM13):c.63C>T (p.Gly21=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1038780	NM_021620.4(PRDM13):c.67C>A (p.Arg23Ser)	PRDM13 (R23S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 838801	NM_021620.4(PRDM13):c.68G>T (p.Arg23Leu)	PRDM13 (R23L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1005927	NM_021620.4(PRDM13):c.70C>G (p.Leu24Val)	PRDM13 (L24V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1570383	NM_021620.4(PRDM13):c.72C>G (p.Leu24=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1482219	NM_021620.4(PRDM13):c.74G>A (p.Gly25Glu)	PRDM13 (G25E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1099123	NM_021620.4(PRDM13):c.93C>T (p.Phe31=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1993752	NM_021620.4(PRDM13):c.95A>G (p.Lys32Arg)	PRDM13 (K32R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1122640	NM_021620.4(PRDM13):c.105G>A (p.Lys35=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 837920	NM_021620.4(PRDM13):c.113C>T (p.Ser38Leu)	PRDM13 (S38L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1118863	NM_021620.4(PRDM13):c.117C>T (p.Asp39=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1093560	NM_021620.4(PRDM13):c.118C>T (p.Arg40Cys)	PRDM13 (R40C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1965354	NM_021620.4(PRDM13):c.119G>A (p.Arg40His)	PRDM13 (R40H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1378802	NM_021620.4(PRDM13):c.119G>T (p.Arg40Leu)	PRDM13 (R40L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2707909	NM_021620.4(PRDM13):c.130G>C (p.Gly44Arg)	PRDM13 (G44R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1500636	NM_021620.4(PRDM13):c.130G>A (p.Gly44Arg)	PRDM13 (G44R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 731098	NM_021620.4(PRDM13):c.134C>T (p.Pro45Leu)	PRDM13 (P45L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1154508	NM_021620.4(PRDM13):c.135T>C (p.Pro45=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1514508	NM_021620.4(PRDM13):c.136A>C (p.Lys46Gln)	PRDM13 (K46Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2771828	NM_021620.4(PRDM13):c.144+1G>C	PRDM13	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 1564742	NM_021620.4(PRDM13):c.144+7A>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1531264	NM_021620.4(PRDM13):c.144+14A>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998100	NM_021620.4(PRDM13):c.144+16A>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1547002	NM_021620.4(PRDM13):c.145-12C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2094870	NM_021620.4(PRDM13):c.145-11T>A	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1575042	NM_021620.4(PRDM13):c.147G>A (p.Val49=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2087583	NM_021620.4(PRDM13):c.148C>T (p.Arg50Cys)	PRDM13 (R50C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1358063	NM_021620.4(PRDM13):c.169G>A (p.Val57Met)	PRDM13 (V57M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1058620	NM_021620.4(PRDM13):c.172_177del (p.Asp58_Glu59del)	PRDM13	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 960817	NM_021620.4(PRDM13):c.185dup (p.Ser63fs)	PRDM13 (S63fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 1059797	NM_021620.4(PRDM13):c.185G>T (p.Gly62Val)	PRDM13 (G62V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1674052	NM_021620.4(PRDM13):c.186C>T (p.Gly62=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1126748	NM_021620.4(PRDM13):c.207G>A (p.Gly69=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2759958	NM_021620.4(PRDM13):c.213C>T (p.Ile71=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1539382	NM_021620.4(PRDM13):c.216G>A (p.Arg72=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1093521	NM_021620.4(PRDM13):c.225A>G (p.Arg75=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2114500	NM_021620.4(PRDM13):c.242C>A (p.Thr81Asn)	PRDM13 (T81N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1961532	NM_021620.4(PRDM13):c.265C>T (p.Pro89Ser)	PRDM13 (P89S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2811188	NM_021620.4(PRDM13):c.268G>A (p.Gly90Arg)	PRDM13 (G90R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1982208	NM_021620.4(PRDM13):c.273A>T (p.Gly91=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1364948	NM_021620.4(PRDM13):c.276+4C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2054734	NM_021620.4(PRDM13):c.276+5T>C	PRDM13	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2129307	NM_021620.4(PRDM13):c.276+19del	PRDM13	Deletion (intron variant)	not provided	GLikely benign
Select item 1674098	NM_021620.4(PRDM13):c.276+18C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1118897	NM_021620.4(PRDM13):c.277-7G>A	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1136886	NM_021620.4(PRDM13):c.291A>C (p.Ala97=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1568703	NM_021620.4(PRDM13):c.292T>C (p.Leu98=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1656915	NM_021620.4(PRDM13):c.294G>A (p.Leu98=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1648139	NM_021620.4(PRDM13):c.300C>T (p.Asp100=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 841792	NM_021620.4(PRDM13):c.301G>A (p.Val101Ile)	PRDM13 (V101I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2009886	NM_021620.4(PRDM13):c.311G>C (p.Gly104Ala)	PRDM13 (G104A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2995823	NM_021620.4(PRDM13):c.336T>C (p.Ser112=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968170	NM_021620.4(PRDM13):c.351G>C (p.Gln117His)	PRDM13 (Q117H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2005001	NM_021620.4(PRDM13):c.352T>C (p.Trp118Arg)	PRDM13 (W118R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1016645	NM_021620.4(PRDM13):c.353G>T (p.Trp118Leu)	PRDM13 (W118L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946998	NM_021620.4(PRDM13):c.358G>A (p.Asp120Asn)	PRDM13 (D120N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1386021	NM_021620.4(PRDM13):c.358G>C (p.Asp120His)	PRDM13 (D120H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1154478	NM_021620.4(PRDM13):c.369C>T (p.Thr123=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1062409	NM_021620.4(PRDM13):c.370A>G (p.Thr124Ala)	PRDM13 (T124A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1931494	NM_021620.4(PRDM13):c.379_380delinsAT (p.Pro127Met)	PRDM13 (P127M)	Indel (missense variant)	not provided	GUncertain significance
Select item 1927646	NM_021620.4(PRDM13):c.380C>T (p.Pro127Leu)	PRDM13 (P127L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1352956	NM_021620.4(PRDM13):c.387C>G (p.His129Gln)	PRDM13 (H129Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2064911	NM_021620.4(PRDM13):c.388G>A (p.Asp130Asn)	PRDM13 (D130N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1602825	NM_021620.4(PRDM13):c.390C>T (p.Asp130=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1047014	NM_021620.4(PRDM13):c.391G>A (p.Glu131Lys)	PRDM13 (E131K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1036660	NM_021620.4(PRDM13):c.397+4C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 855386	NM_021620.4(PRDM13):c.397+6C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667820	NM_021620.4(PRDM13):c.397+7A>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1615316	NM_021620.4(PRDM13):c.397+16G>C	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2061098	NM_021620.4(PRDM13):c.397+17C>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1545623	NM_021620.4(PRDM13):c.397+17C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1963147	NM_021620.4(PRDM13):c.397+18G>A	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2084518	NM_021620.4(PRDM13):c.398-16A>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2039177	NM_021620.4(PRDM13):c.398-15T>C	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2017147	NM_021620.4(PRDM13):c.398-12T>G	PRDM13	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1102050	NM_021620.4(PRDM13):c.398-4C>T	PRDM13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2164570	NM_021620.4(PRDM13):c.398-2A>C	PRDM13	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 1515922	NM_021620.4(PRDM13):c.400G>A (p.Glu134Lys)	PRDM13 (E134K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2968317	NM_021620.4(PRDM13):c.418T>C (p.Trp140Arg)	PRDM13 (W140R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1515995	NM_021620.4(PRDM13):c.421T>A (p.Tyr141Asn)	PRDM13 (Y141N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1958915	NM_021620.4(PRDM13):c.467T>G (p.Leu156Arg)	PRDM13 (L156R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1559775	NM_021620.4(PRDM13):c.477C>T (p.His159=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799410	NM_021620.4(PRDM13):c.487A>G (p.Ser163Gly)	PRDM13 (S163G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1167633	NM_021620.4(PRDM13):c.488G>C (p.Ser163Thr)	PRDM13 (S163T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1299904	NM_021620.4(PRDM13):c.492C>T (p.Gly164=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1345323	NM_021620.4(PRDM13):c.512T>C (p.Leu171Pro)	PRDM13 (L171P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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