ATXN2L[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144327	GRCh38/hg38 16p13.3-11.2(chr16:4644892-29170820)x3	ABAT, ABCC1 +852 more	Copy number gain	See cases	GPathogenic
Select item 151527	GRCh38/hg38 16p12.2-11.2(chr16:21350622-29202837)x3	APOBR, AQP8 +287 more	Copy number gain	See cases	GLikely pathogenic
Select item 58086	GRCh38/hg38 16p12.2-11.2(chr16:21463739-29249579)x3	LOC130058727, LOC130058728 +287 more	Copy number gain	See cases	GPathogenic
Select item 58099	GRCh38/hg38 16p12.2-11.2(chr16:21602183-29314373)x3	OTOA, PALB2 +280 more	Copy number gain	See cases	GPathogenic
Select item 146289	GRCh38/hg38 16p12.2-11.2(chr16:22634385-29227323)x3	APOBR, AQP8 +233 more	Copy number gain	See cases	GLikely pathogenic
Select item 58626	GRCh38/hg38 16p12.2-11.2(chr16:23047969-30632245)x3	DCTPP1, DOC2A +409 more	Copy number gain	See cases	GPathogenic
Select item 152605	GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	LOC130058732, LOC130058733 +504 more	Copy number gain	See cases	GPathogenic
Select item 151637	GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3	ZNF747, ZNF747-DT +378 more	Copy number gain	See cases	GPathogenic
Select item 59292	GRCh38/hg38 16p12.1-11.2(chr16:28293803-29531653)x3	APOBR, ATP2A1 +78 more	Copy number gain	See cases	GUncertain significance
Select item 153260	GRCh38/hg38 16p12.1-11.2(chr16:28320366-29415078)x3	APOBR, ATP2A1 +72 more	Copy number gain	See cases	GUncertain significance
Select item 148782	GRCh38/hg38 16p12.1-11.2(chr16:28327346-29342070)x1	ATP2A1, APOBR +70 more	Copy number loss	See cases	GPathogenic
Select item 545197	NC_000016.10:g.(?_28351819)_(29325073_?)del	APOBR, ATP2A1 +68 more	Deletion	Schizophrenia	GPathogenic
Select item 60446	GRCh38/hg38 16p12.1-11.2(chr16:28366111-30183432)x3	LOC125146439, LOC125146440 +179 more	Copy number gain	See cases	GPathogenic
Select item 150351	GRCh38/hg38 16p12.1-11.2(chr16:28392026-29170879)x3	APOBR, ATP2A1 +61 more	Copy number gain	See cases	GUncertain significance
Select item 152023	GRCh38/hg38 16p12.1-11.2(chr16:28392832-29170875)x1	APOBR, ATP2A1 +61 more	Copy number loss	See cases	GPathogenic
Select item 151177	GRCh38/hg38 16p12.1-11.2(chr16:28392832-30320693)x1	ALDOA, APOBR +187 more	Copy number loss	See cases	GPathogenic
Select item 150642	GRCh38/hg38 16p12.1-11.2(chr16:28392832-29320029)x1	APOBR, ATP2A1 +66 more	Copy number loss	See cases	GPathogenic
Select item 148886	GRCh38/hg38 16p12.1-11.2(chr16:28392832-29342070)x1	APOBR, ATP2A1 +67 more	Copy number loss	See cases	GPathogenic
Select item 148506	GRCh38/hg38 16p12.1-11.2(chr16:28392832-30186020)x1	ALDOA, APOBR +180 more	Copy number loss	See cases	GPathogenic
Select item 58735	GRCh38/hg38 16p12.1-11.2(chr16:28456967-30295107)x1	ALDOA, APOBR +186 more	Copy number loss	See cases	GPathogenic
Select item 148497	GRCh38/hg38 16p12.1-11.2(chr16:28487211-29202837)x3	APOBR, ATP2A1 +61 more	Copy number gain	See cases	GUncertain significance
Select item 154502	GRCh38/hg38 16p12.1-11.2(chr16:28492482-29170875)x3	APOBR, ATP2A1 +57 more	Copy number gain	See cases	GUncertain significance
Select item 146479	GRCh38/hg38 16p12.1-11.2(chr16:28492482-30179247)x3	ALDOA, APOBR +171 more	Copy number gain	See cases	GPathogenic
Select item 146471	GRCh38/hg38 16p12.1-11.2(chr16:28492482-29170875)x1	LOC130058739, LOC130058740 +57 more	Copy number loss	See cases	GLikely pathogenic
Select item 146463	GRCh38/hg38 16p12.1-11.2(chr16:28492482-29320029)x3	APOBR, ATP2A1 +62 more	Copy number gain	See cases	GUncertain significance
Select item 34150	GRCh38/hg38 16p12.1-11.2(chr16:28492482-30179247)x1	ALDOA, APOBR +171 more	Copy number loss	See cases	GPathogenic
Select item 60372	GRCh38/hg38 16p11.2(chr16:28531783-30183432)x1	LOC130058756, LOC130058757 +170 more	Copy number loss	See cases	GPathogenic
Select item 59641	GRCh38/hg38 16p11.2(chr16:28531783-29025786)x1	ATP2A1, ATP2A1-AS1 +48 more	Copy number loss	See cases	GPathogenic
Select item 145658	GRCh38/hg38 16p11.2(chr16:28584316-29019738)x3	ATP2A1, ATP2A1-AS1 +44 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 160911	GRCh38/hg38 16p11.2(chr16:28589904-29030797)x3	ATP2A1, ATP2A1-AS1 +45 more	Copy number gain	See cases	GUncertain significance
Select item 59293	GRCh38/hg38 16p11.2(chr16:28589904-29030797)x3	ATP2A1, ATP2A1-AS1 +45 more	Copy number gain	See cases	GUncertain significance
Select item 59294	GRCh38/hg38 16p11.2(chr16:28592408-29025786)x3	ATP2A1, ATP2A1-AS1 +43 more	Copy number gain	See cases	GUncertain significance
Select item 59295	GRCh38/hg38 16p11.2(chr16:28599237-29025786)x3	ATP2A1, ATP2A1-AS1 +41 more	Copy number gain	See cases	GUncertain significance
Select item 1679691	Single allele	LAT, LOC112340393 +44 more	Deletion	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 155233	GRCh38/hg38 16p11.2(chr16:28677764-29039870)x1	ATP2A1, ATP2A1-AS1 +37 more	Copy number loss	See cases	GPathogenic
Select item 153218	GRCh38/hg38 16p11.2(chr16:28696852-29039870)x1	ATP2A1, ATP2A1-AS1 +37 more	Copy number loss	See cases	GPathogenic
Select item 59643	GRCh38/hg38 16p11.2(chr16:28710478-29025786)x1	ATP2A1, ATP2A1-AS1 +36 more	Copy number loss	See cases	GPathogenic
Select item 59642	GRCh38/hg38 16p11.2(chr16:28710478-29025786)x3	ATP2A1, ATP2A1-AS1 +36 more	Copy number gain	See cases	GUncertain significance
Select item 148525	GRCh38/hg38 16p11.2(chr16:28722418-29033455)x1	ATP2A1, ATP2A1-AS1 +37 more	Copy number loss	See cases	GPathogenic
Select item 155463	GRCh38/hg38 16p11.2(chr16:28807707-29039870)x1	ATP2A1, ATP2A1-AS1 +34 more	Copy number loss	See cases	GPathogenic
Select item 151536	GRCh38/hg38 16p11.2(chr16:28809422-29033455)x1	ATP2A1, ATP2A1-AS1 +34 more	Copy number loss	See cases	GPathogenic
Select item 1184309	NC_000016.10:g.28812342_29035950dup	LOC130058735, ATP2A1 +34 more	Duplication	not provided	GUncertain significance
Select item 149412	GRCh38/hg38 16p11.2(chr16:28813473-29033455)x1	ATP2A1, ATP2A1-AS1 +34 more	Copy number loss	See cases	GPathogenic
Select item 149239	GRCh38/hg38 16p11.2(chr16:28813473-29032639)x1	ATP2A1, ATP2A1-AS1 +34 more	Copy number loss	See cases	GPathogenic
Select item 148483	GRCh38/hg38 16p11.2(chr16:28813473-29122414)x1	ATP2A1, ATP2A1-AS1 +36 more	Copy number loss	See cases	GLikely pathogenic
Select item 145955	GRCh38/hg38 16p11.2(chr16:28813473-29032580)x3	ATP2A1, ATP2A1-AS1 +34 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 59296	GRCh38/hg38 16p11.2(chr16:28813473-28981076)x3	ATP2A1, ATP2A1-AS1 +28 more	Copy number gain	See cases	GUncertain significance
Select item 1326293	GRCh38/hg38 16p11.2(chr16:28814284-29129367)x3	NFATC2IP-AS1, RABEP2 +36 more	Copy number gain	not provided	Gnot provided
Select item 3132247	NM_007245.4(ATXN2L):c.22C>A (p.Gln8Lys)	ATXN2L, LOC130058734 (Q8K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531876	NM_007245.4(ATXN2L):c.52C>A (p.Pro18Thr)	ATXN2L, LOC130058734 (P18T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460967	NM_007245.4(ATXN2L):c.88G>T (p.Gly30Cys)	ATXN2L, LOC130058734 (G30C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467036	NM_007245.4(ATXN2L):c.110G>A (p.Gly37Asp)	ATXN2L, LOC130058734 (G37D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462855	NM_007245.4(ATXN2L):c.131C>A (p.Thr44Asn)	ATXN2L, LOC130058734 (T44N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333139	NM_007245.4(ATXN2L):c.175C>G (p.Leu59Val)	ATXN2L, LOC130058734 (L59V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132245	NM_007245.4(ATXN2L):c.199A>G (p.Ser67Gly)	ATXN2L, LOC130058734 (S67G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276710	NM_007245.4(ATXN2L):c.224G>A (p.Gly75Asp)	ATXN2L, LOC130058734 (G75D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 583588	NC_000016.10:g.(?_28824392)_(28904205_?)del	ATP2A1, ATP2A1-AS1 +13 more	Deletion	Brody myopathy	GPathogenic
Select item 3024379	GRCh38/hg38 16p11.2(chr16:28825316-29028291)	ATP2A1, ATP2A1-AS1 +32 more	Copy number loss	Autism spectrum disorder	GPathogenic
Select item 2282543	NM_007245.4(ATXN2L):c.362C>G (p.Ser121Cys)	ATXN2L (S121C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775041	NM_007245.4(ATXN2L):c.393+8G>A	ATXN2L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 59644	GRCh38/hg38 16p11.2(chr16:28826129-29030797)x1	ATP2A1, ATP2A1-AS1 +33 more	Copy number loss	See cases	GPathogenic
Select item 3132251	NM_007245.4(ATXN2L):c.484G>A (p.Ala162Thr)	ATXN2L (A162T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132252	NM_007245.4(ATXN2L):c.493C>T (p.Arg165Trp)	ATXN2L (R165W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132253	NM_007245.4(ATXN2L):c.523C>T (p.Arg175Cys)	ATXN2L (R175C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540781	NM_007245.4(ATXN2L):c.620A>G (p.Lys207Arg)	ATXN2L (K207R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132254	NM_007245.4(ATXN2L):c.645G>A (p.Met215Ile)	ATXN2L (M215I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546612	NM_007245.4(ATXN2L):c.688C>T (p.Arg230Cys)	ATXN2L (R230C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256214	NM_007245.4(ATXN2L):c.689G>T (p.Arg230Leu)	ATXN2L (R230L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132255	NM_007245.4(ATXN2L):c.877G>C (p.Glu293Gln)	ATXN2L (E237D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255343	NM_007245.4(ATXN2L):c.929G>A (p.Arg310His)	ATXN2L (R310H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333834	NM_007245.4(ATXN2L):c.937A>G (p.Ile313Val)	ATXN2L (I313V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 689662	NM_007245.4(ATXN2L):c.944T>C (p.Met315Thr)	ATXN2L (M315T +1 more)	Single nucleotide variant (missense variant)	Marfanoid habitus and intellectual disability	GUncertain significance
Select item 2325778	NM_007245.4(ATXN2L):c.986C>T (p.Ala329Val)	ATXN2L (A329V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519344	NM_007245.4(ATXN2L):c.1010G>A (p.Arg337Gln)	ATXN2L (G282R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132236	NM_007245.4(ATXN2L):c.1064G>A (p.Arg355Gln)	ATXN2L (E300K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132237	NM_007245.4(ATXN2L):c.1114G>A (p.Gly372Ser)	ATXN2L (G372S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132238	NM_007245.4(ATXN2L):c.1151C>T (p.Pro384Leu)	ATXN2L (L329F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333148	NM_007245.4(ATXN2L):c.1271C>T (p.Ser424Leu)	ATXN2L (S361L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486125	NM_007245.4(ATXN2L):c.1288T>C (p.Ser430Pro)	ATXN2L (S430P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559222	NM_007245.4(ATXN2L):c.1298C>T (p.Thr433Ile)	ATXN2L (T370I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132239	NM_007245.4(ATXN2L):c.1402G>A (p.Gly468Ser)	ATXN2L (G474S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214145	NM_007245.4(ATXN2L):c.1414C>T (p.Pro472Ser)	ATXN2L (P409S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132240	NM_007245.4(ATXN2L):c.1430C>G (p.Ser477Cys)	ATXN2L (S454C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537355	NM_007245.4(ATXN2L):c.1445C>T (p.Ser482Leu)	ATXN2L (S488L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132241	NM_007245.4(ATXN2L):c.1484C>G (p.Ala495Gly)	ATXN2L (A432G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 149864	GRCh38/hg38 16p11.2(chr16:28832433-29019750)x1	ATP2A1, ATP2A1-AS1 +32 more	Copy number loss	See cases	GPathogenic
Select item 149863	GRCh38/hg38 16p11.2(chr16:28832433-29019750)x3	ATP2A1, ATP2A1-AS1 +32 more	Copy number gain	See cases	GUncertain significance
Select item 2620995	NM_007245.4(ATXN2L):c.1529C>G (p.Ser510Cys)	ATXN2L (S447C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132242	NM_007245.4(ATXN2L):c.1541C>G (p.Pro514Arg)	ATXN2L (P514R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1342030	NM_007245.4(ATXN2L):c.1660-15G>A	ATXN2L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2462637	NM_007245.4(ATXN2L):c.1826A>G (p.Lys609Arg)	ATXN2L (K585R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603092	NM_007245.4(ATXN2L):c.1907C>T (p.Pro636Leu)	ATXN2L (P573L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132243	NM_007245.4(ATXN2L):c.1956A>G (p.Glu652=)	ATXN2L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3132244	NM_007245.4(ATXN2L):c.1984A>C (p.Asn662His)	ATXN2L (N639H +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646354	NM_007245.4(ATXN2L):c.1986T>C (p.Asn662=)	ATXN2L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2540460	NM_007245.4(ATXN2L):c.2151C>G (p.Ile717Met)	ATXN2L (I717M +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132246	NM_007245.4(ATXN2L):c.2159G>C (p.Gly720Ala)	ATXN2L (G657A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240864	NM_007245.4(ATXN2L):c.2161C>T (p.Pro721Ser)	ATXN2L (P697S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 714697	NM_007245.4(ATXN2L):c.2412C>T (p.Pro804=)	ATXN2L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3132248	NM_007245.4(ATXN2L):c.2449A>T (p.Met817Leu)	ATXN2L (M793L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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