List of variants in gene VCAN reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 39

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HGVS	dbSNP	gnomAD frequency
NM_004385.5(VCAN):c.9882C>T (p.Val3294=)	rs308365	0.97301
NM_004385.5(VCAN):c.4323G>A (p.Gln1441=)	rs2548541	0.67722
NM_004385.5(VCAN):c.4547A>G (p.Lys1516Arg)	rs309559	0.50554
NM_004385.5(VCAN):c.5808T>C (p.Gly1936=)	rs309557	0.50487
NM_004385.5(VCAN):c.6723A>G (p.Arg2241=)	rs160279	0.50384
NM_004385.5(VCAN):c.348T>C (p.Thr116=)	rs12332199	0.40199
NM_004385.5(VCAN):c.5477G>A (p.Arg1826His)	rs188703	0.38473
NM_004385.5(VCAN):c.645A>G (p.Val215=)	rs4470745	0.33601
NM_004385.5(VCAN):c.1283G>A (p.Gly428Asp)	rs2287926	0.16841
NM_004385.5(VCAN):c.9379+7T>C	rs695103	0.09623
NM_004385.5(VCAN):c.4569A>G (p.Thr1523=)	rs16900528	0.06757
NM_004385.5(VCAN):c.9630C>T (p.His3210=)	rs16900564	0.05374
NM_004385.5(VCAN):c.9033C>A (p.Asn3011Lys)	rs16900532	0.05068
NM_004385.5(VCAN):c.9075G>A (p.Thr3025=)	rs113014073	0.02820
NM_004385.5(VCAN):c.393C>T (p.Asp131=)	rs35042106	0.01920
NM_004385.5(VCAN):c.5155A>T (p.Thr1719Ser)	rs113965318	0.01319
NM_004385.5(VCAN):c.5576C>A (p.Ala1859Glu)	rs34050047	0.01316
NM_004385.5(VCAN):c.6123C>T (p.Ile2041=)	rs113659987	0.01282
NM_004385.5(VCAN):c.8622G>A (p.Ala2874=)	rs3096171	0.01237
NM_004385.5(VCAN):c.899C>T (p.Ser300Leu)	rs2652098	0.00988
NM_004385.5(VCAN):c.4422T>C (p.Thr1474=)	rs61733395	0.00980
NM_004385.5(VCAN):c.9104C>T (p.Ala3035Val)	rs111512368	0.00955
NM_004385.5(VCAN):c.7419C>T (p.Ser2473=)	rs61754536	0.00819
NM_004385.5(VCAN):c.2887C>T (p.Pro963Ser)	rs76914270	0.00597
NM_004385.5(VCAN):c.4604A>G (p.Glu1535Gly)	rs61749614	0.00315
NM_004385.5(VCAN):c.5187G>A (p.Glu1729=)	rs35648048	0.00302
NM_004385.5(VCAN):c.9234G>A (p.Glu3078=)	rs139453864	0.00270
NM_004385.5(VCAN):c.7551C>T (p.Asp2517=)	rs77870162	0.00182
NM_004385.5(VCAN):c.1864T>C (p.Trp622Arg)	rs147152203	0.00142
NM_004385.5(VCAN):c.2666C>T (p.Thr889Ile)	rs149153726	0.00128
NM_004385.5(VCAN):c.1243A>G (p.Ile415Val)	rs141268824	0.00127
NM_004385.5(VCAN):c.2028A>G (p.Leu676=)	rs147286274	0.00127
NM_004385.5(VCAN):c.1895C>T (p.Thr632Met)	rs143729093	0.00030
NM_004385.5(VCAN):c.4546A>G (p.Lys1516Glu)	rs144610900	0.00014
NM_004385.5(VCAN):c.7581C>T (p.Phe2527=)	rs149880697	0.00013
NM_004385.5(VCAN):c.2618T>G (p.Ile873Arg)	rs150395515	0.00006
NM_004385.5(VCAN):c.1400C>T (p.Ser467Phe)	rs115336789
NM_004385.5(VCAN):c.6902T>A (p.Phe2301Tyr)	rs160278
NM_004385.5(VCAN):c.8809G>T (p.Asp2937Tyr)	rs160277

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