List of variants in gene ATRX reported as likely 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: 33

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HGVS	dbSNP	gnomAD frequency
NM_000489.6(ATRX):c.2785= (p.Glu929=)	rs3088074	0.49116
NM_000489.6(ATRX):c.4659T>C (p.His1553=)	rs25641	0.05840
NM_000489.6(ATRX):c.228G>A (p.Ser76=)	rs5959371	0.03016
NM_000489.6(ATRX):c.846C>T (p.Ser282=)	rs148015780	0.00101
NM_000489.6(ATRX):c.4120+4A>C	rs200420513	0.00046
NM_000489.6(ATRX):c.2169G>C (p.Glu723Asp)	rs61752456	0.00041
NM_000489.6(ATRX):c.6405C>T (p.Phe2135=)	rs148659669	0.00023
NM_000489.6(ATRX):c.1467C>T (p.Thr489=)	rs199929884	0.00020
NM_000489.6(ATRX):c.1032C>T (p.Ser344=)	rs143491422	0.00011
NM_000489.6(ATRX):c.1798A>G (p.Ile600Val)	rs375129029	0.00008
NM_000489.6(ATRX):c.1868A>G (p.Lys623Arg)	rs145678415	0.00008
NM_000489.6(ATRX):c.3158C>A (p.Thr1053Asn)	rs151273832	0.00007
NM_000489.6(ATRX):c.2000C>T (p.Pro667Leu)	rs61752457	0.00006
NM_000489.6(ATRX):c.1077G>T (p.Leu359=)	rs782504858	0.00005
NM_000489.6(ATRX):c.4746A>G (p.Thr1582=)	rs782097254	0.00005
NM_000489.6(ATRX):c.3042T>C (p.Asp1014=)	rs140476563	0.00004
NM_000489.6(ATRX):c.5697+13A>C	rs782387510	0.00003
NM_000489.6(ATRX):c.6327-16A>G	rs1457254023	0.00003
NM_000489.6(ATRX):c.7113G>A (p.Ala2371=)	rs782703242	0.00003
NM_000489.6(ATRX):c.4699+9C>T	rs782140505	0.00002
NM_000489.6(ATRX):c.7044A>G (p.Gln2348=)	rs375935735	0.00002
NM_000489.6(ATRX):c.134-3T>A	rs587780287	0.00001
NM_000489.6(ATRX):c.672G>A (p.Ala224=)	rs782223625	0.00001
NM_000489.6(ATRX):c.7072-8T>C	rs782602387	0.00001
NM_000489.6(ATRX):c.134-9C>T	rs782350220
NM_000489.6(ATRX):c.1446A>G (p.Glu482=)	rs886044778
NM_000489.6(ATRX):c.4483A>T (p.Asn1495Tyr)	rs782533736
NM_000489.6(ATRX):c.4810-19A>G	rs1557106791
NM_000489.6(ATRX):c.5271G>A (p.Glu1757=)	rs141240580
NM_000489.6(ATRX):c.5787-24GTTT[4]	rs782072699
NM_000489.6(ATRX):c.654A>G (p.Glu218=)	rs782378258
NM_000489.6(ATRX):c.7158A>G (p.Arg2386=)	rs1557041056
NM_000489.6(ATRX):c.7233C>T (p.Asn2411=)	rs1557034927

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