"Ambry Genetics"[submitter] AND "SYDE2"[gene] - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3172618	NM_032184.2(SYDE2):c.3079T>G (p.Trp1027Gly)	SYDE2 (W1027G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591519	NM_032184.2(SYDE2):c.2987A>C (p.His996Pro)	SYDE2 (H996P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323863	NM_032184.2(SYDE2):c.2978C>T (p.Pro993Leu)	SYDE2 (P993L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322772	NM_032184.2(SYDE2):c.2866A>G (p.Met956Val)	SYDE2 (M956V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172617	NM_032184.2(SYDE2):c.2770A>T (p.Met924Leu)	SYDE2 (M924L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610839	NM_032184.2(SYDE2):c.2677C>A (p.Leu893Ile)	SYDE2 (L893I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530446	NM_032184.2(SYDE2):c.2648A>T (p.Tyr883Phe)	SYDE2 (Y883F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616023	NM_032184.2(SYDE2):c.2597G>A (p.Arg866Gln)	SYDE2 (R866Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479751	NM_032184.2(SYDE2):c.2511A>C (p.Lys837Asn)	SYDE2 (K837N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551808	NM_032184.2(SYDE2):c.2447T>C (p.Val816Ala)	SYDE2 (V816A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480464	NM_032184.2(SYDE2):c.2426A>G (p.Gln809Arg)	SYDE2 (Q809R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2486572	NM_032184.2(SYDE2):c.2407C>T (p.His803Tyr)	SYDE2 (H803Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385847	NM_032184.2(SYDE2):c.2384T>C (p.Met795Thr)	SYDE2 (M795T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360998	NM_032184.2(SYDE2):c.2226G>C (p.Leu742Phe)	SYDE2 (L742F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347035	NM_032184.2(SYDE2):c.2099A>G (p.Lys700Arg)	SYDE2 (K700R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172616	NM_032184.2(SYDE2):c.2095T>C (p.Ser699Pro)	SYDE2 (S699P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383645	NM_032184.2(SYDE2):c.1975G>A (p.Asp659Asn)	SYDE2 (D659N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372876	NM_032184.2(SYDE2):c.1879C>T (p.Pro627Ser)	SYDE2 (P627S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172614	NM_032184.2(SYDE2):c.1821A>C (p.Lys607Asn)	SYDE2 (K607N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172613	NM_032184.2(SYDE2):c.1755G>C (p.Lys585Asn)	SYDE2 (K585N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250972	NM_032184.2(SYDE2):c.1741A>G (p.Thr581Ala)	SYDE2 (T581A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323861	NM_032184.2(SYDE2):c.1700G>A (p.Arg567Gln)	SYDE2 (R567Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3172612	NM_032184.2(SYDE2):c.1670A>C (p.Asn557Thr)	SYDE2 (N557T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621996	NM_032184.2(SYDE2):c.1622G>T (p.Arg541Leu)	SYDE2 (R541L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234629	NM_032184.2(SYDE2):c.1469G>A (p.Ser490Asn)	SYDE2 (S490N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262119	NM_032184.2(SYDE2):c.1399A>G (p.Ile467Val)	SYDE2 (I467V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288197	NM_032184.2(SYDE2):c.1361A>G (p.Gln454Arg)	SYDE2 (Q454R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604198	NM_032184.2(SYDE2):c.1292A>G (p.Asp431Gly)	SYDE2 (D431G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172610	NM_032184.2(SYDE2):c.1240A>G (p.Lys414Glu)	SYDE2 (K414E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392159	NM_032184.2(SYDE2):c.1208A>G (p.Asn403Ser)	SYDE2 (N403S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2520176	NM_032184.2(SYDE2):c.1052C>T (p.Ser351Leu)	SYDE2 (S351L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481913	NM_032184.2(SYDE2):c.1043C>T (p.Ser348Phe)	SYDE2 (S348F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323864	NM_032184.2(SYDE2):c.1033G>A (p.Ala345Thr)	SYDE2 (A345T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323868	NM_032184.2(SYDE2):c.995A>G (p.Lys332Arg)	SYDE2 (K332R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172625	NM_032184.2(SYDE2):c.985T>C (p.Ser329Pro)	SYDE2 (S329P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2565950	NM_032184.2(SYDE2):c.982C>G (p.Gln328Glu)	SYDE2 (Q328E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214469	NM_032184.2(SYDE2):c.958T>C (p.Ser320Pro)	SYDE2 (S320P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484856	NM_032184.2(SYDE2):c.928G>C (p.Asp310His)	SYDE2 (D310H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279079	NM_032184.2(SYDE2):c.878A>G (p.Gln293Arg)	SYDE2 (Q293R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226031	NM_032184.2(SYDE2):c.806A>G (p.Asp269Gly)	SYDE2 (D269G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172623	NM_032184.2(SYDE2):c.773C>T (p.Ser258Leu)	SYDE2 (S258L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206900	NM_032184.2(SYDE2):c.755A>T (p.Glu252Val)	SYDE2 (E252V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323865	NM_032184.2(SYDE2):c.653G>A (p.Gly218Glu)	SYDE2 (G218E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212313	NM_032184.2(SYDE2):c.634A>T (p.Thr212Ser)	SYDE2 (T212S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550307	NM_032184.2(SYDE2):c.469C>T (p.Pro157Ser)	SYDE2 (P157S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323869	NM_032184.2(SYDE2):c.439T>A (p.Cys147Ser)	SYDE2 (C147S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3172621	NM_032184.2(SYDE2):c.429G>T (p.Gln143His)	SYDE2 (Q143H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323867	NM_032184.2(SYDE2):c.424C>T (p.Leu142Phe)	SYDE2 (L142F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172620	NM_032184.2(SYDE2):c.397C>T (p.Arg133Cys)	SYDE2 (R133C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207649	NM_032184.2(SYDE2):c.359C>T (p.Pro120Leu)	SYDE2 (P120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323862	NM_032184.2(SYDE2):c.358C>T (p.Pro120Ser)	SYDE2 (P120S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172619	NM_032184.2(SYDE2):c.310A>G (p.Ser104Gly)	SYDE2 (S104G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323870	NM_032184.2(SYDE2):c.307C>T (p.Pro103Ser)	SYDE2 (P103S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323866	NM_032184.2(SYDE2):c.295T>C (p.Phe99Leu)	SYDE2 (F99L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2552245	NM_032184.2(SYDE2):c.237G>C (p.Met79Ile)	LOC129930865, SYDE2 (M79I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353158	NM_032184.2(SYDE2):c.140G>A (p.Gly47Glu)	LOC129930865, SYDE2 (G47E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359209	NM_032184.2(SYDE2):c.101C>T (p.Ser34Phe)	LOC129930865, SYDE2 (S34F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534655	NM_032184.2(SYDE2):c.76G>A (p.Ala26Thr)	LOC129930865, SYDE2 (A26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172622	NM_032184.2(SYDE2):c.53C>G (p.Ala18Gly)	LOC129930865, SYDE2 (A18G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534654	NM_032184.2(SYDE2):c.26G>T (p.Gly9Val)	LOC129930865, SYDE2 (G9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 60