PRDM1[gene] and "single gene"[properties] - ClinVar

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Items: 64

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2337351	NM_001198.4(PRDM1):c.28G>A (p.Val10Met)	PRDM1 (V10M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511472	NM_001198.4(PRDM1):c.47C>T (p.Ala16Val)	PRDM1 (A16V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527306	NM_001198.4(PRDM1):c.53A>G (p.Lys18Arg)	PRDM1 (K18R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318129	NM_001198.4(PRDM1):c.73A>G (p.Arg25Gly)	PRDM1 (R25G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518743	NM_001198.4(PRDM1):c.75G>C (p.Arg25Ser)	PRDM1 (R25S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309737	NM_001198.4(PRDM1):c.189C>T (p.Asn63=)	PRDM1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 135074	NM_001198.4(PRDM1):c.220G>A (p.Gly74Ser)	PRDM1 (G74S)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2509525	NM_001198.4(PRDM1):c.230T>C (p.Val77Ala)	PRDM1 (V77A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3053989	NM_001198.4(PRDM1):c.239A>T (p.Glu80Val)	PRDM1 (E80V)	Single nucleotide variant (missense variant)	PRDM1-related disorder	GLikely benign
Select item 2293809	NM_001198.4(PRDM1):c.250C>G (p.Pro84Ala)	PRDM1 (P84A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 666912	NM_001198.4(PRDM1):c.281del (p.Asn94fs)	PRDM1 (N94fs)	Deletion (frameshift variant)	not specified	GUncertain significance
Select item 716138	NM_001198.4(PRDM1):c.387C>T (p.Asn129=)	PRDM1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3309740	NM_001198.4(PRDM1):c.500C>T (p.Ser167Phe)	PRDM1 (S167F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135075	NM_001198.4(PRDM1):c.502C>G (p.Pro168Ala)	PRDM1 (P168A +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 3309734	NM_001198.4(PRDM1):c.604C>T (p.Arg202Trp)	PRDM1 (R68W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218322	NM_001198.4(PRDM1):c.605G>A (p.Arg202Gln)	PRDM1 (R68Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135076	NM_001198.4(PRDM1):c.609C>G (p.Asp203Glu)	PRDM1 (D203E +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3309736	NM_001198.4(PRDM1):c.640G>A (p.Gly214Arg)	PRDM1 (G80R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218323	NM_001198.4(PRDM1):c.652A>G (p.Met218Val)	PRDM1 (M218V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407114	NM_001198.4(PRDM1):c.674A>G (p.Gln225Arg)	PRDM1 (Q91R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410177	NM_001198.4(PRDM1):c.740A>G (p.Glu247Gly)	PRDM1 (E113G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218324	NM_001198.4(PRDM1):c.784A>G (p.Lys262Glu)	PRDM1 (K262E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135078	NM_001198.4(PRDM1):c.811A>G (p.Ile271Val)	PRDM1 (I271V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2210764	NM_001198.4(PRDM1):c.841G>A (p.Asp281Asn)	PRDM1 (D147N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135085	NM_001198.4(PRDM1):c.857G>C (p.Arg286Pro)	PRDM1 (R286P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2464371	NM_001198.4(PRDM1):c.931A>C (p.Lys311Gln)	PRDM1 (K177Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592271	NM_001198.4(PRDM1):c.1010C>A (p.Pro337His)	PRDM1 (P203H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135086	NM_001198.4(PRDM1):c.1061G>A (p.Ser354Asn)	PRDM1 (S354N +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135081	NM_001198.4(PRDM1):c.1100C>T (p.Ser367Phe)	PRDM1 (S367F +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2555621	NM_001198.4(PRDM1):c.1136C>A (p.Ala379Glu)	PRDM1 (A245E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135088	NM_001198.4(PRDM1):c.1141T>C (p.Tyr381His)	PRDM1 (Y381H +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135079	NM_001198.4(PRDM1):c.1147A>G (p.Thr383Ala)	PRDM1 (T383A +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135082	NM_001198.4(PRDM1):c.1148C>T (p.Thr383Met)	PRDM1 (T383M +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 3218316	NM_001198.4(PRDM1):c.1156T>A (p.Leu386Met)	PRDM1 (L252M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309739	NM_001198.4(PRDM1):c.1172G>A (p.Gly391Asp)	PRDM1 (G391D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293608	NM_001198.4(PRDM1):c.1192C>G (p.Leu398Val)	PRDM1 (L264V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268435	NM_001198.4(PRDM1):c.1195C>T (p.Pro399Ser)	PRDM1 (P399S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656804	NM_001198.4(PRDM1):c.1207A>G (p.Ile403Val)	PRDM1 (I269V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 135087	NM_001198.4(PRDM1):c.1222G>C (p.Ala408Pro)	PRDM1 (A408P +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135080	NM_001198.4(PRDM1):c.1306A>G (p.Asn436Asp)	PRDM1 (N436D +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2532568	NM_001198.4(PRDM1):c.1327C>G (p.Leu443Val)	PRDM1 (L309V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261344	NM_001198.4(PRDM1):c.1346A>G (p.Asn449Ser)	PRDM1 (N315S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135083	NM_001198.4(PRDM1):c.1348C>T (p.Leu450Phe)	PRDM1 (L450F +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2225021	NM_001198.4(PRDM1):c.1358G>A (p.Gly453Glu)	PRDM1 (G453E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293808	NM_001198.4(PRDM1):c.1388C>T (p.Pro463Leu)	PRDM1 (P463L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218318	NM_001198.4(PRDM1):c.1396C>T (p.Leu466Phe)	PRDM1 (L332F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135084	NM_001198.4(PRDM1):c.1400C>T (p.Pro467Leu)	PRDM1 (P467L +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2269320	NM_001198.4(PRDM1):c.1460T>C (p.Val487Ala)	PRDM1 (V487A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551872	NM_001198.4(PRDM1):c.1474C>T (p.Pro492Ser)	PRDM1 (P358S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050600	NM_001198.4(PRDM1):c.1557G>A (p.Ala519=)	PRDM1	Single nucleotide variant (synonymous variant)	PRDM1-related disorder	GLikely benign
Select item 3309742	NM_001198.4(PRDM1):c.1591C>T (p.Pro531Ser)	PRDM1 (P397S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304403	NM_001198.4(PRDM1):c.1609G>A (p.Ala537Thr)	PRDM1 (A403T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218320	NM_001198.4(PRDM1):c.1630G>A (p.Asp544Asn)	PRDM1 (D544N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 748986	NM_001198.4(PRDM1):c.1881A>G (p.Gly627=)	PRDM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3309733	NM_001198.4(PRDM1):c.1948C>A (p.Leu650Met)	PRDM1 (L516M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3055453	NM_001198.4(PRDM1):c.1961C>T (p.Ser654Phe)	PRDM1 (S520F +1 more)	Single nucleotide variant (missense variant)	PRDM1-related disorder	GUncertain significance
Select item 3309735	NM_001198.4(PRDM1):c.2048G>A (p.Arg683Gln)	PRDM1 (R549Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371702	NM_001198.4(PRDM1):c.2141C>T (p.Pro714Leu)	PRDM1 (P580L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520216	NM_001198.4(PRDM1):c.2186A>T (p.Glu729Val)	PRDM1 (E595V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135090	NM_001198.4(PRDM1):c.2233G>A (p.Val745Met)	PRDM1 (V745M +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 2234470	NM_001198.4(PRDM1):c.2284G>A (p.Val762Met)	PRDM1 (V628M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 135091	NM_001198.4(PRDM1):c.2312G>A (p.Gly771Asp)	PRDM1 (G771D +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 3218321	NM_001198.4(PRDM1):c.2414G>A (p.Ser805Asn)	PRDM1 (S671N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135089	NM_001198.4(PRDM1):c.2464C>A (p.Pro822Thr)	PRDM1 (P822T +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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Items: 64