List of variants in gene ADAR reported as likely pathogenic for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.577C>G (p.Pro193Ala)	rs145588689	0.00162
NM_001111.5(ADAR):c.1602-2A>G
NM_001111.5(ADAR):c.1786-1G>C
NM_001111.5(ADAR):c.2763-1G>A
NM_001111.5(ADAR):c.2763-2A>G	rs2101579172
NM_001111.5(ADAR):c.2886-1del	rs1696896431
NM_001111.5(ADAR):c.2997G>T (p.Lys999Asn)	rs398122896
NM_001111.5(ADAR):c.3019G>A (p.Gly1007Arg)	rs398122822
NM_001111.5(ADAR):c.3215G>T (p.Ser1072Ile)	rs1553207540
NM_001111.5(ADAR):c.3254_3255del (p.Thr1085fs)	rs2101563488
NM_001111.5(ADAR):c.3286C>T (p.Arg1096Ter)	rs769148365
NM_001111.5(ADAR):c.3335A>T (p.Tyr1112Phe)	rs398122895
NM_001111.5(ADAR):c.3337G>C (p.Asp1113His)	rs398122894
NM_001111.5(ADAR):c.3363dup (p.Lys1122Ter)	rs1571046959
NM_001111.5(ADAR):c.3364A>C (p.Lys1122Gln)
NM_001111.5(ADAR):c.665_666insGGAGCCAAGGAGCCCCAAA (p.Asn222fs)	rs1571110158
NM_001111.5(ADAR):c.758G>A (p.Trp253Ter)	rs2101642015

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