C3469542[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

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Items: 54

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 241697	NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser)	SLX4 (N1834S)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 414716	NM_032444.4(SLX4):c.5259C>T (p.Asp1753=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GBenign
Select item 456335	NM_032444.4(SLX4):c.5250G>A (p.Ala1750=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 241694	NM_032444.4(SLX4):c.5146T>A (p.Ser1716Thr)	SLX4 (S1716T)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 241693	NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser)	SLX4 (G1534S)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 262054	NM_032444.4(SLX4):c.4581G>A (p.Pro1527=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 262053	NM_032444.4(SLX4):c.4500T>C (p.Asn1500=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 241692	NM_032444.4(SLX4):c.4485G>C (p.Ala1495=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GLikely benign
Select item 241690	NM_032444.4(SLX4):c.4338C>T (p.Thr1446=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GBenign/Likely benign
Select item 241688	NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln)	SLX4 (R1372Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 241685	NM_032444.4(SLX4):c.3963G>A (p.Pro1321=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 262051	NM_032444.4(SLX4):c.3868C>A (p.His1290Asn)	SLX4 (H1290N)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 262050	NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe)	SLX4 (S1271F)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GBenign
Select item 262049	NM_032444.4(SLX4):c.3783G>A (p.Pro1261=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 215952	NM_032444.4(SLX4):c.3774C>T (p.Pro1258=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GConflicting classifications of pathogenicity
Select item 456313	NM_032444.4(SLX4):c.3676C>T (p.Arg1226Trp)	SLX4 (R1226W)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 262048	NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val)	SLX4 (A1221V)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 262047	NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu)	SLX4 (P1122L)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 456307	NM_032444.4(SLX4):c.3245A>G (p.Gln1082Arg)	SLX4 (Q1082R)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GBenign/Likely benign
Select item 414713	NM_032444.4(SLX4):c.3189C>T (p.Gly1063=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GConflicting classifications of pathogenicity
Select item 262046	NM_032444.4(SLX4):c.3162G>A (p.Ser1054=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GBenign
Select item 414702	NM_032444.4(SLX4):c.3109T>C (p.Leu1037=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GBenign
Select item 215537	NM_032444.4(SLX4):c.2854_2855delinsAT (p.Ala952Met)	SLX4 (A952M)	Indel (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 262044	NM_032444.4(SLX4):c.2854G>A (p.Ala952Thr)	SLX4 (A952T)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GBenign
Select item 235273	NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln)	SLX4 (E942Q)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 241674	NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser)	SLX4 (A916S)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 241673	NM_032444.4(SLX4):c.2628C>T (p.Asp876=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GBenign/Likely benign
Select item 262042	NM_032444.4(SLX4):c.2160+50C>T	SLX4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 414707	NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp)	SLX4 (E701D)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +4 more	GConflicting classifications of pathogenicity
Select item 262041	NM_032444.4(SLX4):c.2013+23G>A	SLX4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 262040	NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser)	SLX4 (L671S)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GBenign
Select item 241668	NM_032444.4(SLX4):c.1898G>A (p.Gly633Asp)	SLX4 (G633D)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 414712	NM_032444.4(SLX4):c.1896G>C (p.Gly632=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 262038	NM_032444.4(SLX4):c.1803G>A (p.Ser601=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 414729	NM_032444.4(SLX4):c.1802C>T (p.Ser601Leu)	SLX4 (S601L)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign
Select item 414726	NM_032444.4(SLX4):c.1706C>T (p.Pro569Leu)	SLX4 (P569L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GLikely benign
Select item 414724	NM_032444.4(SLX4):c.1470C>T (p.Leu490=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GLikely benign
Select item 262035	NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys)	SLX4 (N457K)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 262034	NM_032444.4(SLX4):c.1366+11T>C	SLX4	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 262033	NM_032444.4(SLX4):c.1163+10C>T	SLX4	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign
Select item 262031	NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr)	SLX4 (P385T)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GBenign/Likely benign
Select item 241702	NM_032444.4(SLX4):c.999C>T (p.Ile333=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GBenign
Select item 456339	NM_032444.4(SLX4):c.833G>A (p.Arg278Gln)	SLX4 (R278Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GConflicting classifications of pathogenicity
Select item 262058	NM_032444.4(SLX4):c.753G>A (p.Ala251=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GBenign
Select item 376971	NM_032444.4(SLX4):c.718A>G (p.Asn240Asp)	SLX4 (N240D)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 212222	NM_032444.4(SLX4):c.710G>A (p.Arg237Gln)	SLX4 (R237Q)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 262057	NM_032444.4(SLX4):c.678C>T (p.His226=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 262056	NM_032444.4(SLX4):c.610C>T (p.Arg204Cys)	SLX4 (R204C)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GBenign
Select item 262055	NM_032444.4(SLX4):c.555C>T (p.Asp185=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GBenign
Select item 456322	NM_032444.4(SLX4):c.426T>A (p.Gly142=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GConflicting classifications of pathogenicity
Select item 241679	NM_032444.4(SLX4):c.336G>A (p.Pro112=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 436787	NM_032444.4(SLX4):c.165C>T (p.Cys55=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GLikely benign
Select item 241701	NM_032444.4(SLX4):c.90C>T (p.Ser30=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 407911	NM_032444.4(SLX4):c.86G>A (p.Arg29His)	SLX4 (R29H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GConflicting classifications of pathogenicity

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Items: 54