IFNAR1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688073	NM_000629.3(IFNAR1):c.77-22T>G	IFNAR1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2713151	NM_000629.3(IFNAR1):c.77-9C>T	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2123867	NM_000629.3(IFNAR1):c.84A>G (p.Lys28=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1467748	NM_000629.3(IFNAR1):c.86A>G (p.Asn29Ser)	IFNAR1 (N29S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1932077	NM_000629.3(IFNAR1):c.93A>C (p.Lys31Asn)	IFNAR1 (K31N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2991649	NM_000629.3(IFNAR1):c.100C>T (p.Gln34Ter)	IFNAR1 (Q34*)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 1478473	NM_000629.3(IFNAR1):c.102A>G (p.Gln34=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2968348	NM_000629.3(IFNAR1):c.114C>T (p.Val38=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1006414	NM_000629.3(IFNAR1):c.115G>A (p.Asp39Asn)	IFNAR1 (D39N)	Single nucleotide variant (missense variant +1 more)	not provided	GConflicting classifications of pathogenicity
Select item 2234802	NM_000629.3(IFNAR1):c.128A>G (p.Asp43Gly)	IFNAR1 (D43G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1404568	NM_000629.3(IFNAR1):c.130A>C (p.Asn44His)	IFNAR1 (N44H)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2428780	NM_000629.3(IFNAR1):c.131A>C (p.Asn44Thr)	IFNAR1 (N44T)	Single nucleotide variant (missense variant +1 more)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 1508375	NM_000629.3(IFNAR1):c.131A>G (p.Asn44Ser)	IFNAR1 (N44S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1667152	NM_000629.3(IFNAR1):c.132C>T (p.Asn44=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2727949	NM_000629.3(IFNAR1):c.141G>C (p.Leu47=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1412746	NM_000629.3(IFNAR1):c.157G>A (p.Asp53Asn)	IFNAR1 (D53N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1567811	NM_000629.3(IFNAR1):c.168C>T (p.Val56=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1431648	NM_000629.3(IFNAR1):c.169G>A (p.Gly57Arg)	IFNAR1 (G57R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2070005	NM_000629.3(IFNAR1):c.181T>G (p.Phe61Val)	IFNAR1 (F61V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 715750	NM_000629.3(IFNAR1):c.189C>T (p.Phe63=)	IFNAR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1398350	NM_000629.3(IFNAR1):c.190G>A (p.Asp64Asn)	IFNAR1 (D64N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1361002	NM_000629.3(IFNAR1):c.190G>T (p.Asp64Tyr)	IFNAR1 (D64Y)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2114900	NM_000629.3(IFNAR1):c.193T>C (p.Tyr65His)	IFNAR1 (Y65H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1481917	NM_000629.3(IFNAR1):c.200+2del	IFNAR1	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 1900213	NM_000629.3(IFNAR1):c.200+5G>T	IFNAR1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1557379	NM_000629.3(IFNAR1):c.200+11C>G	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2688255	NM_000629.3(IFNAR1):c.200+108A>G	IFNAR1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1652344	NM_000629.3(IFNAR1):c.201-22_201-19del	IFNAR1	Deletion (intron variant)	not provided	GBenign
Select item 1997025	NM_000629.3(IFNAR1):c.201-19T>C	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1657736	NM_000629.3(IFNAR1):c.201-10dup	IFNAR1	Duplication (intron variant)	not provided	GBenign
Select item 1538833	NM_000629.3(IFNAR1):c.201-18del	IFNAR1	Deletion (intron variant)	not provided	GLikely benign
Select item 2025023	NM_000629.3(IFNAR1):c.201-12T>A	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1899110	NM_000629.3(IFNAR1):c.205G>C (p.Gly69Arg)	IFNAR1 (G69R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1713674	NM_000629.3(IFNAR1):c.206G>A (p.Gly69Glu)	IFNAR1 (G69E)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1410722	NM_000629.3(IFNAR1):c.211G>T (p.Asp71Tyr)	IFNAR1 (D2Y +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 778906	NM_000629.3(IFNAR1):c.213T>C (p.Asp71=)	IFNAR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3108279	NM_000629.3(IFNAR1):c.218G>C (p.Trp73Ser)	IFNAR1 (W4S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1929813	NM_000629.3(IFNAR1):c.219G>C (p.Trp73Cys)	IFNAR1 (W4C +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2720948	NM_000629.3(IFNAR1):c.222A>C (p.Ile74=)	IFNAR1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2767189	NM_000629.3(IFNAR1):c.227dup (p.Leu76fs)	IFNAR1 (L76fs +1 more)	Duplication (frameshift variant +2 more)	not provided	GPathogenic
Select item 1387079	NM_000629.3(IFNAR1):c.235T>C (p.Cys79Arg)	IFNAR1 (C79R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2025845	NM_000629.3(IFNAR1):c.252dup (p.Thr85fs)	IFNAR1 (T85fs +1 more)	Duplication (frameshift variant +2 more)	not provided	GPathogenic
Select item 2535337	NM_000629.3(IFNAR1):c.272C>T (p.Ser91Leu)	IFNAR1 (S22L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1525268	NM_000629.3(IFNAR1):c.278A>G (p.Lys93Arg)	IFNAR1 (K93R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1061428	NM_000629.3(IFNAR1):c.284A>G (p.Asn95Ser)	IFNAR1 (N26S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1947226	NM_000629.3(IFNAR1):c.285T>C (p.Asn95=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1503232	NM_000629.3(IFNAR1):c.286G>T (p.Val96Phe)	IFNAR1 (V96F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2006398	NM_000629.3(IFNAR1):c.291T>A (p.Tyr97Ter)	IFNAR1 (Y97* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2542605	NM_000629.3(IFNAR1):c.299T>C (p.Ile100Thr)	IFNAR1 (I100T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2075545	NM_000629.3(IFNAR1):c.308G>A (p.Arg103His)	IFNAR1 (R103H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1525850	NM_000629.3(IFNAR1):c.310A>G (p.Ile104Val)	IFNAR1 (I104V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1358290	NM_000629.3(IFNAR1):c.317C>T (p.Ala106Val)	IFNAR1 (A106V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1666278	NM_000629.3(IFNAR1):c.318A>T (p.Ala106=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2709301	NM_000629.3(IFNAR1):c.333T>G (p.Thr111=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1997698	NM_000629.3(IFNAR1):c.335C>A (p.Ser112Tyr)	IFNAR1 (S112Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2428779	NM_000629.3(IFNAR1):c.341G>C (p.Trp114Ser)	IFNAR1 (W114S +1 more)	Single nucleotide variant (missense variant +1 more)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 2785345	NM_000629.3(IFNAR1):c.354C>T (p.Asp118=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1501733	NM_000629.3(IFNAR1):c.360del (p.Phe120fs)	IFNAR1 (F51fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 1477562	NM_000629.3(IFNAR1):c.358T>C (p.Phe120Leu)	IFNAR1 (F120L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1494375	NM_000629.3(IFNAR1):c.370C>T (p.Arg124Cys)	IFNAR1 (R124C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2191609	NM_000629.3(IFNAR1):c.371G>A (p.Arg124His)	IFNAR1 (R124H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1656064	NM_000629.3(IFNAR1):c.376+15C>G	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1649397	NM_000629.3(IFNAR1):c.377-13G>C	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2786784	NM_000629.3(IFNAR1):c.377-12A>T	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1609025	NM_000629.3(IFNAR1):c.377-11T>C	IFNAR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1498680	NM_000629.3(IFNAR1):c.377-2A>G	IFNAR1	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 3108280	NM_000629.3(IFNAR1):c.380A>C (p.Gln127Pro)	IFNAR1 (Q127P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542080	NM_000629.3(IFNAR1):c.392C>T (p.Pro131Leu)	IFNAR1 (P131L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1485456	NM_000629.3(IFNAR1):c.397G>T (p.Val133Leu)	IFNAR1 (V133L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2071817	NM_000629.3(IFNAR1):c.444T>C (p.Pro148=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1511753	NM_000629.3(IFNAR1):c.460G>T (p.Val154Phe)	IFNAR1 (V154F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1720249	NM_000629.3(IFNAR1):c.464T>G (p.Met155Arg)	IFNAR1 (M155R +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3108281	NM_000629.3(IFNAR1):c.470C>T (p.Ala157Val)	IFNAR1 (A3V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3018313	NM_000629.3(IFNAR1):c.472T>C (p.Leu158=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2872028	NM_000629.3(IFNAR1):c.473T>C (p.Leu158Ser)	IFNAR1 (L158S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3108282	NM_000629.3(IFNAR1):c.478G>A (p.Gly160Ser)	IFNAR1 (G6S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1640096	NM_000629.3(IFNAR1):c.498C>T (p.Ser166=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1414935	NM_000629.3(IFNAR1):c.501_503del (p.Leu167_Val168delinsPhe)	IFNAR1	Deletion (inframe_indel +1 more)	not provided	GUncertain significance
Select item 1170802	NM_000629.3(IFNAR1):c.502G>C (p.Val168Leu)	IFNAR1 (V14L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign
Select item 1166208	NM_000629.3(IFNAR1):c.504T>C (p.Val168=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1404509	NM_000629.3(IFNAR1):c.506del (p.Ile169fs)	IFNAR1 (I15fs +2 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2180842	NM_000629.3(IFNAR1):c.516C>T (p.Asn172=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1595038	NM_000629.3(IFNAR1):c.516C>G (p.Asn172Lys)	IFNAR1 (N103K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2323740	NM_000629.3(IFNAR1):c.518C>G (p.Ser173Cys)	IFNAR1 (S104C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1967049	NM_000629.3(IFNAR1):c.518C>T (p.Ser173Phe)	IFNAR1 (S173F +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1972985	NM_000629.3(IFNAR1):c.531+2T>G	IFNAR1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 1633259	NM_000629.3(IFNAR1):c.531+12T>G	IFNAR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3022947	NM_000629.3(IFNAR1):c.532-15A>T	IFNAR1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1378891	NM_000629.3(IFNAR1):c.547A>G (p.Ile183Val)	IFNAR1 (I114V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2477893	NM_000629.3(IFNAR1):c.548T>G (p.Ile183Ser)	IFNAR1 (I183S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283563	NM_000629.3(IFNAR1):c.560A>G (p.His187Arg)	IFNAR1 (H118R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1355487	NM_000629.3(IFNAR1):c.603A>C (p.Lys201Asn)	IFNAR1 (K47N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1460571	NM_000629.3(IFNAR1):c.623C>T (p.Thr208Met)	IFNAR1 (T139M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 1169450	NM_000629.3(IFNAR1):c.624G>A (p.Thr208=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1475170	NM_000629.3(IFNAR1):c.637G>A (p.Gly213Ser)	IFNAR1 (G59S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2994380	NM_000629.3(IFNAR1):c.639T>C (p.Gly213=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1383370	NM_000629.3(IFNAR1):c.644A>G (p.Tyr215Cys)	IFNAR1 (Y61C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2004555	NM_000629.3(IFNAR1):c.646A>G (p.Ser216Gly)	IFNAR1 (S216G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1609586	NM_000629.3(IFNAR1):c.651A>G (p.Pro217=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2789627	NM_000629.3(IFNAR1):c.660T>C (p.Cys220=)	IFNAR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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