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

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2462995	NM_005066.3(SFPQ):c.1955C>G (p.Thr652Ser)	SFPQ (T652S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160889	NM_005066.3(SFPQ):c.1526A>C (p.Glu509Ala)	SFPQ (E509A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477017	NM_005066.3(SFPQ):c.1322C>T (p.Thr441Ile)	SFPQ (T441I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317851	NM_005066.3(SFPQ):c.1216G>A (p.Asp406Asn)	SFPQ (D406N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160888	NM_005066.3(SFPQ):c.1064C>T (p.Thr355Ile)	SFPQ (T355I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242267	NM_005066.3(SFPQ):c.964G>A (p.Glu322Lys)	SFPQ (E322K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533676	NM_005066.3(SFPQ):c.799C>G (p.Arg267Gly)	LOC129930101, SFPQ (R267G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596897	NM_005066.3(SFPQ):c.748C>T (p.Pro250Ser)	LOC129930101, SFPQ (P250S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230041	NM_005066.3(SFPQ):c.743A>C (p.His248Pro)	LOC129930101, SFPQ (H248P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364038	NM_005066.3(SFPQ):c.739C>T (p.His247Tyr)	LOC129930101, SFPQ (H247Y)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2517615	NM_005066.3(SFPQ):c.629G>C (p.Gly210Ala)	LOC129930102, SFPQ (G210A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254618	NM_005066.3(SFPQ):c.524C>T (p.Pro175Leu)	LOC129930102, SFPQ (P175L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160891	NM_005066.3(SFPQ):c.452C>G (p.Pro151Arg)	LOC129930102, SFPQ (P151R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616142	NM_005066.3(SFPQ):c.421G>T (p.Ala141Ser)	LOC129930102, SFPQ (A141S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365365	NM_005066.3(SFPQ):c.410C>A (p.Pro137Gln)	LOC129930102, SFPQ (P137Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337688	NM_005066.3(SFPQ):c.305C>G (p.Pro102Arg)	SFPQ (P102R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274281	NM_005066.3(SFPQ):c.294G>C (p.Gln98His)	SFPQ (Q98H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317850	NM_005066.3(SFPQ):c.251C>T (p.Pro84Leu)	SFPQ (P84L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592141	NM_005066.3(SFPQ):c.229C>T (p.Pro77Ser)	SFPQ (P77S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250342	NM_005066.3(SFPQ):c.185C>T (p.Pro62Leu)	SFPQ (P62L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160890	NM_005066.3(SFPQ):c.166C>T (p.Pro56Ser)	SFPQ (P56S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230042	NM_005066.3(SFPQ):c.83T>C (p.Leu28Pro)	SFPQ (L28P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339066	NM_005066.3(SFPQ):c.76G>A (p.Gly26Ser)	SFPQ (G26S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 23