List of variants in gene ADAR reported as likely benign for not provided

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.1760A>G (p.Tyr587Cys)	rs17843865	0.01046
NM_001111.5(ADAR):c.1601+317C>T	rs142654985	0.00881
NM_001111.5(ADAR):c.*309T>G	rs141369769	0.00402
NM_001111.5(ADAR):c.3020-137C>T	rs141130161	0.00367
NM_001111.5(ADAR):c.1935-261G>C	rs186653551	0.00355
NM_001111.5(ADAR):c.1003A>T (p.Ile335Phe)	rs34154757	0.00235
NM_001111.5(ADAR):c.1926T>C (p.His642=)	rs150171059	0.00135
NM_001111.5(ADAR):c.2886-11_2886-10del	rs557801982	0.00128
NM_001111.5(ADAR):c.3018C>T (p.Asn1006=)	rs151241634	0.00063
NM_001111.5(ADAR):c.3523A>C (p.Arg1175=)	rs146625055	0.00042
NM_001111.5(ADAR):c.2052G>A (p.Ala684=)	rs148041309	0.00039
NM_001111.5(ADAR):c.772G>A (p.Gly258Arg)	rs201143561	0.00039
NM_001111.5(ADAR):c.1625A>G (p.Asn542Ser)	rs200242235	0.00016
NM_001111.5(ADAR):c.1725C>T (p.Ala575=)	rs144279106	0.00014
NM_001111.5(ADAR):c.1934+8C>T	rs376025865	0.00013
NM_001111.5(ADAR):c.1935-20C>T	rs17843867	0.00012
NM_001111.5(ADAR):c.2274C>T (p.Phe758=)	rs149039619	0.00011
NM_001111.5(ADAR):c.222G>A (p.Arg74=)	rs150423721	0.00010
NM_001111.5(ADAR):c.1392T>C (p.Asn464=)	rs370763473	0.00009
NM_001111.5(ADAR):c.1192A>G (p.Asn398Asp)	rs371050239	0.00006
NM_001111.5(ADAR):c.1875A>G (p.Lys625=)	rs771871176	0.00006
NM_001111.5(ADAR):c.3171G>A (p.Leu1057=)	rs149496690	0.00006
NM_001111.5(ADAR):c.57C>T (p.Gly19=)	rs137983302	0.00006
NM_001111.5(ADAR):c.675G>A (p.Pro225=)	rs771459105	0.00004
NM_001111.5(ADAR):c.1158C>T (p.Asn386=)	rs752276168	0.00001
NM_001111.5(ADAR):c.1189T>A (p.Ser397Thr)	rs1190740301	0.00001
NM_001111.5(ADAR):c.30C>T (p.Ser10=)	rs769752403	0.00001
NM_001111.5(ADAR):c.3351A>G (p.Gln1117=)	rs1571047056	0.00001
NM_001111.5(ADAR):c.474A>C (p.Ala158=)	rs1434133622	0.00001
NM_001111.5(ADAR):c.15+241TG[11]	rs551880161
NM_001111.5(ADAR):c.15+259_15+268del	rs66550822
NM_001111.5(ADAR):c.2262C>T (p.His754=)
NM_001111.5(ADAR):c.2496+41_2496+42dup
NM_001111.5(ADAR):c.2497-91C>T	rs115161953

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