ClinVar for PubMed (Select 22911665) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2052686	NM_032444.4(SLX4):c.2013+2T>C	SLX4	Single nucleotide variant (splice donor variant)	Fanconi anemia	GLikely pathogenic
Select item 929627	NM_032444.4(SLX4):c.1925-95G>A	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929626	NM_032444.4(SLX4):c.1925-106T>G	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929625	NM_032444.4(SLX4):c.1925-122C>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929624	NM_032444.4(SLX4):c.1924+127G>A	SLX4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 929623	NM_032444.4(SLX4):c.1924+59C>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929622	NM_032444.4(SLX4):c.1924+5G>A	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929621	NM_032444.4(SLX4):c.1736T>C (p.Leu579Pro)	SLX4 (L579P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929619	NM_032444.4(SLX4):c.1517G>A (p.Ser506Asn)	SLX4 (S506N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929618	NM_032444.4(SLX4):c.5440C>T (p.Arg1814Cys)	SLX4 (R1814C)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 929617	NM_032444.4(SLX4):c.5081C>T (p.Ala1694Val)	SLX4 (A1694V)	Single nucleotide variant (missense variant)	SLX4-related disorder +1 more	GUncertain significance
Select item 929616	NM_032444.4(SLX4):c.4887C>T (p.Leu1629=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GLikely benign
Select item 929615	NM_032444.4(SLX4):c.4739+90C>G	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929614	NM_032444.4(SLX4):c.4739+79G>A	SLX4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 929613	NM_032444.4(SLX4):c.4739+31G>A	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929612	NM_032444.4(SLX4):c.4739+24G>T	SLX4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 929611	NM_032444.4(SLX4):c.4637-110T>C	SLX4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 929610	NM_032444.4(SLX4):c.4637-210A>G	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929609	NM_032444.4(SLX4):c.4637-227C>T	SLX4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 929608	NM_032444.4(SLX4):c.4637-234G>A	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929607	NM_032444.4(SLX4):c.4637-267C>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929606	NM_032444.4(SLX4):c.4272C>T (p.Asp1424=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GLikely benign
Select item 929604	NM_032444.4(SLX4):c.1513G>A (p.Ala505Thr)	SLX4 (A505T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929602	NM_032444.4(SLX4):c.1367-44G>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929601	NM_032444.4(SLX4):c.1164C>G (p.Ser388Arg)	SLX4 (S388R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929600	NM_032444.4(SLX4):c.1163+194C>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929598	NM_032444.4(SLX4):c.1132C>A (p.Pro378Thr)	SLX4 (P378T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929597	NM_032444.4(SLX4):c.3860T>G (p.Val1287Gly)	SLX4 (V1287G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929596	NM_032444.4(SLX4):c.2949C>T (p.Tyr983=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GLikely benign
Select item 929594	NM_032444.4(SLX4):c.950+29C>T	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929593	NM_032444.4(SLX4):c.851A>G (p.His284Arg)	SLX4 (H284R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 929592	NM_032444.4(SLX4):c.761-32T>G	SLX4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 929591	NM_032444.4(SLX4):c.536-80C>T	SLX4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 929589	NM_032444.4(SLX4):c.2328-48_2328-36del	SLX4	Deletion (intron variant)	not specified	GLikely benign
Select item 929588	NM_032444.4(SLX4):c.2161-136G>A	SLX4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 929587	NM_032444.4(SLX4):c.2014-28G>A	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929586	NM_032444.4(SLX4):c.2013+137G>C	SLX4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 929585	NM_032444.4(SLX4):c.2013+130C>G	SLX4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 929584	NM_032444.4(SLX4):c.2013+2T>A	SLX4	Single nucleotide variant (splice donor variant)	not provided	GPathogenic
Select item 929583	NM_032444.4(SLX4):c.237T>C (p.Ala79=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 837545	NM_032444.4(SLX4):c.3019C>A (p.Gln1007Lys)	SLX4 (Q1007K)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GConflicting classifications of pathogenicity
Select item 837025	NM_032444.4(SLX4):c.4410G>A (p.Pro1470=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GLikely benign
Select item 700333	NM_032444.4(SLX4):c.1641G>A (p.Thr547=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GLikely benign
Select item 698410	NM_032444.4(SLX4):c.2667A>G (p.Gln889=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GLikely benign
Select item 697233	NM_032444.4(SLX4):c.4797C>T (p.Phe1599=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GLikely benign
Select item 653251	NM_032444.4(SLX4):c.1702G>A (p.Val568Met)	SLX4 (V568M)	Single nucleotide variant (missense variant)	Fanconi anemia	GUncertain significance
Select item 456328	NM_032444.4(SLX4):c.465A>G (p.Glu155=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +2 more	GLikely benign
Select item 456309	NM_032444.4(SLX4):c.3315C>T (p.Ser1105=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia	GBenign
Select item 456300	NM_032444.4(SLX4):c.2328-9G>C	SLX4	Single nucleotide variant (intron variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 436793	NM_032444.4(SLX4):c.3368C>A (p.Ser1123Tyr)	SLX4 (S1123Y)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 436784	NM_032444.4(SLX4):c.1845C>T (p.Leu615=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GLikely benign
Select item 436779	NM_032444.4(SLX4):c.4024A>G (p.Ser1342Gly)	SLX4 (S1342G)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GConflicting classifications of pathogenicity
Select item 436777	NM_032444.4(SLX4):c.4530G>T (p.Leu1510=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GConflicting classifications of pathogenicity
Select item 414702	NM_032444.4(SLX4):c.3109T>C (p.Leu1037=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GBenign
Select item 414700	NM_032444.4(SLX4):c.3178C>T (p.Arg1060Trp)	SLX4 (R1060W)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GConflicting classifications of pathogenicity
Select item 407938	NM_032444.4(SLX4):c.2359G>A (p.Glu787Lys)	SLX4 (E787K)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GConflicting classifications of pathogenicity
Select item 407935	NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu)	SLX4 (K458E)	Single nucleotide variant (missense variant)	Fanconi anemia +4 more	GConflicting classifications of pathogenicity
Select item 407931	NM_032444.4(SLX4):c.4261A>T (p.Ile1421Phe)	SLX4 (I1421F)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GConflicting classifications of pathogenicity
Select item 407905	NM_032444.4(SLX4):c.1271C>T (p.Ala424Val)	SLX4 (A424V)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 319164	NM_032444.4(SLX4):c.2681T>G (p.Val894Gly)	SLX4 (V894G)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 319141	NM_032444.4(SLX4):c.*113C>T	SLX4	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 262058	NM_032444.4(SLX4):c.753G>A (p.Ala251=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
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)	not specified +3 more	GBenign
Select item 262055	NM_032444.4(SLX4):c.555C>T (p.Asp185=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +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)	Fanconi anemia complementation group P +3 more	GBenign
Select item 262050	NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe)	SLX4 (S1271F)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 262049	NM_032444.4(SLX4):c.3783G>A (p.Pro1261=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GBenign
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)	Fanconi anemia complementation group P +3 more	GBenign
Select item 262046	NM_032444.4(SLX4):c.3162G>A (p.Ser1054=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 262042	NM_032444.4(SLX4):c.2160+50C>T	SLX4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
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)	not specified +3 more	GBenign
Select item 262039	NM_032444.4(SLX4):c.1925-30G>A	SLX4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely 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 262037	NM_032444.4(SLX4):c.1755C>T (p.Pro585=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely 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)	Fanconi anemia complementation group P +3 more	GBenign
Select item 262033	NM_032444.4(SLX4):c.1163+10C>T	SLX4	Single nucleotide variant (intron variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 262032	NM_032444.4(SLX4):c.1156A>G (p.Met386Val)	SLX4 (M386V)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GBenign
Select item 262031	NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr)	SLX4 (P385T)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 262030	NM_032444.4(SLX4):c.1152A>G (p.Pro384=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GBenign
Select item 262029	NM_032444.4(SLX4):c.*8A>G	SLX4	Single nucleotide variant (3 prime UTR variant)	not specified +2 more	GBenign
Select item 241702	NM_032444.4(SLX4):c.999C>T (p.Ile333=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 241701	NM_032444.4(SLX4):c.90C>T (p.Ser30=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +3 more	GBenign/Likely benign
Select item 241698	NM_032444.4(SLX4):c.590T>C (p.Val197Ala)	SLX4 (V197A)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GConflicting classifications of pathogenicity
Select item 241697	NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser)	SLX4 (N1834S)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GConflicting classifications of pathogenicity
Select item 241691	NM_032444.4(SLX4):c.4427C>G (p.Thr1476Ser)	SLX4 (T1476S)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 241689	NM_032444.4(SLX4):c.421G>T (p.Gly141Trp)	SLX4 (G141W)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 241685	NM_032444.4(SLX4):c.3963G>A (p.Pro1321=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 241684	NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val)	SLX4 (A1286V)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 241677	NM_032444.4(SLX4):c.2924C>T (p.Pro975Leu)	SLX4 (P975L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +3 more	GBenign/Likely benign
Select item 241676	NM_032444.4(SLX4):c.2786C>T (p.Pro929Leu)	SLX4 (P929L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GBenign
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 241672	NM_032444.4(SLX4):c.2609C>T (p.Ala870Val)	SLX4 (A870V)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GConflicting classifications of pathogenicity
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 215538	NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp)	SLX4 (R1550W)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
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

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