"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARID1B"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3036532	NM_001374828.1(ARID1B):c.269C>G (p.Ala90Gly)	ARID1B, LOC115308161 +1 more (A7G +1 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 2629103	NM_001374828.1(ARID1B):c.275C>G (p.Ala92Gly)	ARID1B, LOC115308161 +1 more (A92G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 126337	NM_001374828.1(ARID1B):c.318G>A (p.Ala106=)	LOC115308161, LOC129997523 +1 more	Single nucleotide variant (synonymous variant)	ARID1B-related disorder +4 more	GBenign/Likely benign
Select item 588042	NM_001374828.1(ARID1B):c.352TCC[8] (p.Ser124dup)	ARID1B, LOC115308161	Microsatellite (inframe_insertion)	not specified +3 more	GBenign/Likely benign
Select item 210267	NM_001374828.1(ARID1B):c.352TCC[6] (p.Ser124del)	ARID1B, LOC115308161 (S124del)	Microsatellite (inframe_deletion)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 3057572	NM_001374828.1(ARID1B):c.360C>T (p.Ser120=)	ARID1B, LOC115308161	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 1196255	NM_001374828.1(ARID1B):c.373GCGGCGGCA[3] (p.Ala128_Ala130dup)	ARID1B, LOC115308161	Microsatellite (inframe_insertion)	not provided +1 more	GLikely benign
Select item 589423	NM_001374828.1(ARID1B):c.381A>G (p.Ala127=)	ARID1B, LOC115308161	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 210272	NM_001374828.1(ARID1B):c.446A>G (p.Asn149Ser)	ARID1B, LOC115308161 +1 more (N66S +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2636969	NM_001374828.1(ARID1B):c.488C>A (p.Pro163His)	ARID1B, LOC115308161 (P163H +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 3058452	NM_001374828.1(ARID1B):c.495G>A (p.Gln165=)	ARID1B, LOC115308161	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 589067	NM_001374828.1(ARID1B):c.506ACCACCACCATGCCCACCACC[1] (p.169HHHHAHH[1])	ARID1B, LOC115308161	Microsatellite (inframe_deletion)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 588419	NM_001374828.1(ARID1B):c.501CCA[4] (p.His172del)	ARID1B, LOC115308161 (H172del)	Microsatellite (inframe_deletion)	not provided +2 more	GBenign/Likely benign
Select item 2628888	NM_001374828.1(ARID1B):c.591GCA[17] (p.Gln214_His215insGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +2 more)	ARID1B-related disorder	GUncertain significance
Select item 2171589	NM_001374828.1(ARID1B):c.588C>T (p.Phe196=)	ARID1B, LOC115308161	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GLikely benign
Select item 589183	NM_001374828.1(ARID1B):c.594GCAGCAGCAGCAGCAGCAACAGCA[3] (p.Gln207_Gln214dup)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 126327	NM_001374828.1(ARID1B):c.591GCA[8] (p.Gln214dup)	LOC115308161, ARID1B	Microsatellite (non-coding transcript variant +1 more)	ARID1B-related disorder +3 more	GBenign/Likely benign
Select item 975342	NM_001374828.1(ARID1B):c.591GCA[4] (p.Gln212_Gln214del)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +1 more)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 591903	NM_001374828.1(ARID1B):c.594GCAGCAGCAGCAGCAGCAACAGCA[1] (p.Gln207_Gln214del)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +1 more)	not provided +2 more	GLikely benign
Select item 589060	NM_001374828.1(ARID1B):c.591GCA[6] (p.Gln214del)	ARID1B, LOC115308161 (Q214del)	Microsatellite (non-coding transcript variant +1 more)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 434350	NM_001374828.1(ARID1B):c.612_632del (p.Gln208_Gln214del)	ARID1B, LOC115308161	Deletion (inframe_deletion +1 more)	ARID1B-related disorder +3 more	GLikely benign
Select item 210285	NM_001374828.1(ARID1B):c.612_620del (p.Gln212_Gln214del)	ARID1B, LOC115308161	Deletion (inframe_deletion +1 more)	not provided +3 more	GLikely benign
Select item 1733407	NM_001374828.1(ARID1B):c.612_617dup (p.Gln214_His215insGlnGln)	ARID1B, LOC115308161	Duplication (non-coding transcript variant +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2041239	NM_001374828.1(ARID1B):c.612_617del (p.Gln213_Gln214del)	ARID1B, LOC115308161	Deletion (non-coding transcript variant +2 more)	not provided +1 more	GLikely benign
Select item 588939	NM_001374828.1(ARID1B):c.615GCA[10] (p.Gln212_Gln214dup)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +1 more)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 210289	NM_001374828.1(ARID1B):c.615GCA[8] (p.Gln214dup)	ARID1B, LOC115308161	Microsatellite (non-coding transcript variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 210288	NM_001374828.1(ARID1B):c.615GCA[6] (p.Gln214del)	ARID1B, LOC115308161 (Q214del)	Microsatellite (non-coding transcript variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 3046610	NM_001374828.1(ARID1B):c.655A>G (p.Asn219Asp)	ARID1B, LOC115308161 (N136D +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	ARID1B-related disorder	GUncertain significance
Select item 3032841	NM_001374828.1(ARID1B):c.660C>T (p.Asn220=)	ARID1B, LOC115308161	Single nucleotide variant (non-coding transcript variant +1 more)	ARID1B-related disorder	GLikely benign
Select item 1969013	NM_001374828.1(ARID1B):c.679_690del (p.Gly227_Ala230del)	ARID1B, LOC115308161	Deletion (non-coding transcript variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3032044	NM_001374828.1(ARID1B):c.808G>A (p.Asp270Asn)	ARID1B, LOC115308161 +1 more (D129N +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	ARID1B-related disorder	GUncertain significance
Select item 1230590	NM_001374828.1(ARID1B):c.852G>A (p.Glu284=)	ARID1B, LOC129997525	Single nucleotide variant (synonymous variant)	ARID1B-related disorder +2 more	GBenign/Likely benign
Select item 3052126	NM_001374828.1(ARID1B):c.900G>C (p.Val300=)	ARID1B, LOC129997525	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 3045815	NM_001374828.1(ARID1B):c.918C>A (p.Gly306=)	ARID1B, LOC129997525	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 434352	NM_001374828.1(ARID1B):c.963C>T (p.Ala321=)	ARID1B	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 3059337	NM_001374828.1(ARID1B):c.966T>G (p.Pro322=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 2630488	NM_001374828.1(ARID1B):c.980_981delinsGT (p.Pro327Arg)	ARID1B (P186R +2 more)	Indel (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 1267132	NM_001374828.1(ARID1B):c.980C>G (p.Pro327Arg)	ARID1B (P327R)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2735057	NM_001374828.1(ARID1B):c.981C>T (p.Pro327=)	ARID1B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2628883	NM_001374828.1(ARID1B):c.986G>C (p.Gly329Ala)	ARID1B (G188A +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 1762477	NM_001374828.1(ARID1B):c.1058CCG[4] (p.Ala357del)	ARID1B (A357del +2 more)	Microsatellite (inframe_indel +1 more)	Inborn genetic diseases +1 more	GBenign
Select item 1492620	NM_001374828.1(ARID1B):c.1075G>C (p.Ala359Pro)	ARID1B (A359P)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2038419	NM_001374828.1(ARID1B):c.1170CGG[11] (p.Gly402_Ser403insGlyGlyGly)	ARID1B	Microsatellite (inframe_indel +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 210312	NM_001374828.1(ARID1B):c.1170CGG[10] (p.Gly401_Gly402dup)	ARID1B	Microsatellite (inframe_insertion)	ARID1B-related disorder +3 more	GBenign/Likely benign
Select item 589538	NM_001374828.1(ARID1B):c.1170CGG[7] (p.Gly402del)	ARID1B (G402del)	Microsatellite (inframe_deletion)	not provided +2 more	GBenign/Likely benign
Select item 445786	NM_001374828.1(ARID1B):c.1170CGG[4] (p.Gly399_Gly402del)	ARID1B	Microsatellite (inframe_deletion)	ARID1B-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 434371	NM_001374828.1(ARID1B):c.1170CGG[5] (p.Gly400_Gly402del)	ARID1B	Microsatellite (inframe_deletion)	ARID1B-related disorder +4 more	GBenign/Likely benign
Select item 3034313	NM_001374828.1(ARID1B):c.1188C>A (p.Gly396=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 589228	NM_001374828.1(ARID1B):c.1194AGG[5] (p.Gly402dup)	ARID1B	Microsatellite (inframe_insertion)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 434353	NM_001374828.1(ARID1B):c.1194A>C (p.Gly398=)	ARID1B	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 589786	NM_001374828.1(ARID1B):c.1211GAG[11] (p.Gly409_Gly411dup)	ARID1B	Microsatellite (inframe_insertion)	not provided +2 more	GBenign/Likely benign
Select item 588854	NM_001374828.1(ARID1B):c.1211GAG[10] (p.Gly410_Gly411dup)	ARID1B	Microsatellite (inframe_insertion)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 210314	NM_001374828.1(ARID1B):c.1211GAG[9] (p.Gly411dup)	ARID1B	Microsatellite (inframe_insertion)	not provided +3 more	GBenign/Likely benign
Select item 591999	NM_001374828.1(ARID1B):c.1211GAG[4] (p.Gly408_Gly411del)	ARID1B	Microsatellite (inframe_deletion)	not provided +2 more	GLikely benign
Select item 434373	NM_001374828.1(ARID1B):c.1211GAG[7] (p.Gly411del)	ARID1B (G411del)	Microsatellite (inframe_deletion)	ARID1B-related disorder +3 more	GBenign
Select item 434354	NM_001374828.1(ARID1B):c.1211GAG[6] (p.Gly410_Gly411del)	ARID1B	Microsatellite (inframe_deletion)	not provided +3 more	GBenign/Likely benign
Select item 434355	NM_001374828.1(ARID1B):c.1227AGGAGGAGCAGGAGC[1] (p.411GAGAG[1])	ARID1B	Microsatellite (inframe_deletion)	not provided +3 more	GBenign/Likely benign
Select item 588355	NM_001374828.1(ARID1B):c.1235CAGGAG[3] (p.412AG[3])	ARID1B	Microsatellite (inframe_insertion)	ARID1B-related disorder +2 more	GBenign/Likely benign
Select item 452366	NM_001374828.1(ARID1B):c.1229G>C (p.Gly410Ala)	ARID1B (G327A +1 more)	Single nucleotide variant (missense variant)	Coffin-Siris syndrome 1 +3 more	GConflicting classifications of pathogenicity
Select item 434375	NM_001374828.1(ARID1B):c.1235CAGGAG[1] (p.412AG[1])	ARID1B	Microsatellite (inframe_deletion)	ARID1B-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 591728	NM_001374828.1(ARID1B):c.1235_1243del (p.Ala412_Ala414del)	ARID1B	Deletion (inframe_deletion)	not provided +1 more	GUncertain significance
Select item 210315	NM_001374828.1(ARID1B):c.1238GAGCAGGAG[1] (p.413GAG[1])	ARID1B	Microsatellite (inframe_deletion)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2716826	NM_001374828.1(ARID1B):c.1241C>G (p.Ala414Gly)	ARID1B (A273G +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2633037	NM_001374828.1(ARID1B):c.1247_1261dup (p.Gly420_Ala421insGlyAlaGlyAlaGly)	ARID1B	Duplication (inframe_indel +1 more)	ARID1B-related disorder	GUncertain significance
Select item 2716828	NM_001374828.1(ARID1B):c.1244G>C (p.Gly415Ala)	ARID1B (G274A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3036623	NM_001374828.1(ARID1B):c.1245AGGAGC[1] (p.416GA[2])	ARID1B	Microsatellite (inframe_indel +1 more)	ARID1B-related disorder	GUncertain significance
Select item 588072	NM_001374828.1(ARID1B):c.1265_1270dup (p.Val422_Ala423dup)	ARID1B	Duplication (inframe_insertion)	Inborn genetic diseases +3 more	GLikely benign
Select item 506613	NM_001374828.1(ARID1B):c.1278_1292del (p.Ala429_Ala433del)	ARID1B	Deletion (inframe_deletion)	ARID1B-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 589736	NM_001374828.1(ARID1B):c.1278_1289del (p.Ala430_Ala433del)	ARID1B	Deletion (inframe_deletion)	not provided +2 more	GLikely benign
Select item 2039951	NM_001374828.1(ARID1B):c.1270G>A (p.Ala424Thr)	ARID1B (A341T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1773009	NM_001374828.1(ARID1B):c.1281GGC[6] (p.Ala433_Gly434insAlaAla)	ARID1B	Microsatellite (inframe_indel +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 589688	NM_001374828.1(ARID1B):c.1281GGC[5] (p.Ala433dup)	ARID1B	Microsatellite (inframe_insertion)	not provided +2 more	GLikely benign
Select item 3056657	NM_001374828.1(ARID1B):c.1281GGC[3] (p.Ala433del)	ARID1B (A292del +2 more)	Microsatellite (inframe_indel +1 more)	ARID1B-related disorder	GLikely benign
Select item 1273955	NM_001374828.1(ARID1B):c.1280C>T (p.Ala427Val)	ARID1B (A427V)	Single nucleotide variant (missense variant)	ARID1B-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 985116	NM_001374828.1(ARID1B):c.1293_1314del (p.Gly434fs)	ARID1B (G434fs)	Deletion (frameshift variant)	Inborn genetic diseases +2 more	GPathogenic
Select item 210265	NM_001374828.1(ARID1B):c.1292CAG[4] (p.Ala433dup)	ARID1B	Microsatellite (inframe_insertion)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1781697	NM_001374828.1(ARID1B):c.1303GGC[8] (p.Gly440_Tyr441insGlyGly)	ARID1B	Microsatellite (inframe_indel +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3033522	NM_001374828.1(ARID1B):c.1340G>A (p.Gly447Glu)	ARID1B (G306E +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 2632554	NM_001374828.1(ARID1B):c.1391G>A (p.Gly464Asp)	ARID1B (G323D +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 1205073	NM_001374828.1(ARID1B):c.1452C>T (p.Gly484=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder +1 more	GBenign/Likely benign
Select item 126312	NM_001374828.1(ARID1B):c.1534A>G (p.Met512Val)	ARID1B (M429V +1 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder +4 more	GBenign/Likely benign
Select item 3041955	NM_001374828.1(ARID1B):c.1587G>C (p.Pro529=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 3041318	NM_001374828.1(ARID1B):c.1590G>C (p.Pro530=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 1770436	NM_001374828.1(ARID1B):c.1593G>C (p.Pro531=)	ARID1B	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 3030288	NM_001374828.1(ARID1B):c.1602G>T (p.Ser534=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 588198	NM_001374828.1(ARID1B):c.1619CGG[3] (p.Ala543del)	ARID1B (A543del)	Microsatellite (inframe_deletion)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1771060	NM_001374828.1(ARID1B):c.1620G>T (p.Ala540=)	ARID1B	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 3037469	NM_001374828.1(ARID1B):c.1623G>T (p.Ala541=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 2891615	NM_001374828.1(ARID1B):c.1631_1636dup (p.Ala545_Ala546insGlyAla)	ARID1B	Duplication (inframe_indel +1 more)	ARID1B-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3060140	NM_001374828.1(ARID1B):c.1629G>T (p.Ala543=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 2389084	NM_001374828.1(ARID1B):c.1631G>C (p.Gly544Ala)	ARID1B (G544A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3060436	NM_001374828.1(ARID1B):c.1635G>T (p.Ala545=)	ARID1B	Single nucleotide variant (synonymous variant)	ARID1B-related disorder	GLikely benign
Select item 3055171	NM_001374828.1(ARID1B):c.1679A>G (p.Lys560Arg)	ARID1B (K419R +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 2628635	NM_001374828.1(ARID1B):c.1680G>C (p.Lys560Asn)	ARID1B (K419N +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 2628574	NM_001374828.1(ARID1B):c.1712C>T (p.Pro571Leu)	ARID1B (P430L +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 1197199	NM_001374828.1(ARID1B):c.1771C>T (p.Pro591Ser)	ARID1B (P591S)	Single nucleotide variant (missense variant)	ARID1B-related disorder +2 more	GBenign/Likely benign
Select item 1558619	NM_001374828.1(ARID1B):c.1791+6C>T	ARID1B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2635231	NM_001374828.1(ARID1B):c.1872G>T (p.Gln624His)	ARID1B (Q483H +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 2635015	NM_001374828.1(ARID1B):c.1918C>G (p.Arg640Gly)	ARID1B (R499G +2 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder	GUncertain significance
Select item 126316	NM_001374828.1(ARID1B):c.1927A>G (p.Ile643Val)	ARID1B (I560V +1 more)	Single nucleotide variant (missense variant)	ARID1B-related disorder +3 more	GBenign

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