C0019562[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 342396	NM_000551.3(VHL):c.-207C>T	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome +3 more	GUncertain significance
Select item 342397	NM_000551.3(VHL):c.-195G>A	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome +2 more	GBenign
Select item 900507	NM_000551.3(VHL):c.-188G>A	VHL	Single nucleotide variant	not specified +1 more	GUncertain significance
Select item 900508	NM_000551.3(VHL):c.-179G>A	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342398	NM_000551.3(VHL):c.-166C>T	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342399	NM_000551.3(VHL):c.-125C>A	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902166	NM_000551.3(VHL):c.-118C>T	VHL	Single nucleotide variant	Von Hippel-Lindau syndrome	GUncertain significance
Select item 256649	NM_000551.3(VHL):c.-77C>T	VHL	Single nucleotide variant	not specified +2 more	GBenign/Likely benign
Select item 560736	NM_000551.3(VHL):c.-73C>T	VHL	Single nucleotide variant	Nonpapillary renal cell carcinoma +4 more	GConflicting classifications of pathogenicity
Select item 342400	NM_000551.4(VHL):c.-64C>T	VHL	Single nucleotide variant (5 prime UTR variant)	VHL-related condition +4 more	GConflicting classifications of pathogenicity
Select item 137904	NM_000551.4(VHL):c.-35G>A	VHL	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 342401	NM_000551.4(VHL):c.-30C>T	VHL	Single nucleotide variant (5 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902167	NM_000551.4(VHL):c.-26C>T	VHL	Single nucleotide variant (5 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 135406	NM_000551.4(VHL):c.3G>A (p.Met1Ile)	VHL (M1I)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 182981	NM_000551.4(VHL):c.5C>T (p.Pro2Leu)	VHL (P2L)	Single nucleotide variant (missense variant)	Von Hippel-Lindau syndrome +5 more	GConflicting classifications of pathogenicity
Select item 342402	NM_000551.4(VHL):c.10A>T (p.Arg4Trp)	VHL (R4W)	Single nucleotide variant (missense variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342403	NM_000551.4(VHL):c.11G>T (p.Arg4Met)	VHL (R4M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 93330	NM_000551.4(VHL):c.74C>T (p.Pro25Leu)	VHL (P25L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 456595	NM_000551.4(VHL):c.99G>C (p.Ser33=)	VHL	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 456569	NM_000551.4(VHL):c.105C>G (p.Ala35=)	VHL	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 43596	NM_000551.4(VHL):c.150C>G (p.Ala50=)	VHL	Single nucleotide variant (synonymous variant)	Von Hippel-Lindau syndrome +4 more	GBenign/Likely benign
Select item 135951	NM_000551.4(VHL):c.183C>G (p.Pro61=)	VHL	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 2233	NM_000551.4(VHL):c.241C>T (p.Pro81Ser)	VHL (P81S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 526692	NM_000551.4(VHL):c.291C>G (p.Pro97=)	VHL	Single nucleotide variant (synonymous variant)	Chuvash polycythemia +2 more	GConflicting classifications of pathogenicity
Select item 36901	NM_000551.4(VHL):c.340+5G>C	VHL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 386138	NM_000551.4(VHL):c.341-5G>A	LOC107303340, VHL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 371833	NM_000551.4(VHL):c.439A>G (p.Ile147Val)	LOC107303340, VHL (I147V)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GUncertain significance
Select item 127830	NM_000551.4(VHL):c.463+8C>T	LOC107303340, VHL	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 456589	NM_000551.4(VHL):c.464-10G>A	LOC107303340, VHL	Single nucleotide variant (intron variant)	Von Hippel-Lindau syndrome +2 more	GBenign/Likely benign
Select item 220655	NM_000551.4(VHL):c.544A>G (p.Arg182Gly)	LOC107303340, VHL (R182G +1 more)	Single nucleotide variant (missense variant +1 more)	Von Hippel-Lindau syndrome +3 more	GConflicting classifications of pathogenicity
Select item 421558	NM_000551.4(VHL):c.599G>A (p.Arg200Gln)	LOC107303340, VHL (R200Q +1 more)	Single nucleotide variant (missense variant +1 more)	Von Hippel-Lindau syndrome +4 more	GConflicting classifications of pathogenicity
Select item 127828	NM_000551.4(VHL):c.629G>A (p.Arg210Gln)	LOC107303340, VHL (R210Q +1 more)	Single nucleotide variant (missense variant +1 more)	Von Hippel-Lindau syndrome +5 more	GConflicting classifications of pathogenicity
Select item 182990	NM_000551.4(VHL):c.631A>C (p.Met211Leu)	LOC107303340, VHL (M211L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 342404	NM_000551.4(VHL):c.639T>C (p.Asp213=)	LOC107303340, VHL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 900550	NM_000551.4(VHL):c.*20C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 900551	NM_000551.4(VHL):c.*70C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome +3 more	GBenign/Likely benign
Select item 342405	NM_000551.4(VHL):c.266_269del	LOC107303340, VHL	Deletion (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 900552	NM_000551.4(VHL):c.*275C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342406	NM_000551.4(VHL):c.*280A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342407	NM_000551.4(VHL):c.*294G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 342408	NM_000551.4(VHL):c.*303A>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 902226	NM_000551.4(VHL):c.*327G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342409	NM_000551.4(VHL):c.*349G>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902227	NM_000551.4(VHL):c.*370A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342410	NM_000551.4(VHL):c.*385del	LOC107303340, VHL	Deletion (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902228	NM_000551.4(VHL):c.*391C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342411	NM_000551.4(VHL):c.*392G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902229	NM_000551.4(VHL):c.*432C>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342412	NM_000551.4(VHL):c.*448G>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902230	NM_000551.4(VHL):c.*452G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902231	NM_000551.4(VHL):c.*522G>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342413	NM_000551.4(VHL):c.*523del	LOC107303340, VHL	Deletion (3 prime UTR variant)	Von Hippel-Lindau syndrome	GLikely benign
Select item 902232	NM_000551.4(VHL):c.*572T>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342414	NM_000551.4(VHL):c.*574T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 903105	NM_000551.4(VHL):c.*579G>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342415	NM_000551.4(VHL):c.*597G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342416	NM_000551.4(VHL):c.*635G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342417	NM_000551.4(VHL):c.*687C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 903106	NM_000551.4(VHL):c.*713T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 903107	NM_000551.4(VHL):c.*718T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342418	NM_000551.4(VHL):c.*724T>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342419	NM_000551.4(VHL):c.*816G>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342420	NM_000551.4(VHL):c.*820A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342421	NM_000551.4(VHL):c.*823G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GLikely benign
Select item 899481	NM_000551.4(VHL):c.*876G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 899482	NM_000551.4(VHL):c.*885T>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342422	NM_000551.4(VHL):c.*923GTTTT[5]	LOC107303340, VHL	Microsatellite (3 prime UTR variant)	Von Hippel-Lindau syndrome	GLikely benign
Select item 342423	NM_000551.4(VHL):c.*989C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 899483	NM_000551.4(VHL):c.*1001T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342424	NM_000551.4(VHL):c.*1023G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342425	NM_000551.4(VHL):c.*1060C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342426	NM_000551.4(VHL):c.*1072C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 900618	NM_000551.4(VHL):c.*1087G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 900619	NM_000551.4(VHL):c.*1114C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342427	NM_000551.4(VHL):c.*1172C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 900620	NM_000551.4(VHL):c.*1181G>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342428	NM_000551.4(VHL):c.*1207G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902299	NM_000551.4(VHL):c.*1222A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342429	NM_000551.4(VHL):c.*1249G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342430	NM_000551.4(VHL):c.*1281A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902300	NM_000551.4(VHL):c.*1301G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342431	NM_000551.4(VHL):c.*1328C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342432	NM_000551.4(VHL):c.*1330A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342433	NM_000551.4(VHL):c.*1347C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 902301	NM_000551.4(VHL):c.*1351G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342434	NM_000551.4(VHL):c.*1371A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342435	NM_000551.4(VHL):c.*1419A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342436	NM_000551.4(VHL):c.*1452A>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342437	NM_000551.4(VHL):c.*1465C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GLikely benign
Select item 342438	NM_000551.4(VHL):c.*1481G>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342439	NM_000551.4(VHL):c.*1513A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 976590	NM_000551.4(VHL):c.*1542C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342440	NM_000551.4(VHL):c.*1617G>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342441	NM_000551.4(VHL):c.*1619T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 342442	NM_000551.4(VHL):c.*1643C>A	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342443	NM_000551.4(VHL):c.*1677C>T	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342444	NM_000551.4(VHL):c.*1680T>C	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign
Select item 899553	NM_000551.4(VHL):c.*1689A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342445	NM_000551.4(VHL):c.*1691A>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GUncertain significance
Select item 342446	NM_000551.4(VHL):c.*1721C>G	LOC107303340, VHL	Single nucleotide variant (3 prime UTR variant)	Von Hippel-Lindau syndrome	GBenign

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