List of variants in gene KCND3 reported as likely benign for Spinocerebellar ataxia type 19/22

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: 123

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1456A>G (p.Thr486Ala)	rs149008060	0.00077
NM_001378969.1(KCND3):c.1573A>G (p.Met525Val)	rs145890206	0.00076
NM_001378969.1(KCND3):c.5C>A (p.Ala2Glu)	rs201340369	0.00066
NM_001378969.1(KCND3):c.1959C>T (p.Ser653=)	rs147087785	0.00027
NM_001378969.1(KCND3):c.1106+10C>T	rs377267051	0.00016
NM_001378969.1(KCND3):c.1292G>A (p.Arg431His)	rs771703569	0.00015
NM_001378969.1(KCND3):c.696G>A (p.Ala232=)	rs370453605	0.00014
NM_001378969.1(KCND3):c.1865C>T (p.Ala622Val)	rs199663609	0.00012
NM_001378969.1(KCND3):c.1702C>T (p.Arg568Cys)	rs144120746	0.00011
NM_001378969.1(KCND3):c.1062C>A (p.Ile354=)	rs150934088	0.00009
NM_001378969.1(KCND3):c.1149C>T (p.Phe383=)	rs760817061	0.00009
NM_001378969.1(KCND3):c.1766+3G>A	rs748524463	0.00009
NM_001378969.1(KCND3):c.207G>A (p.Thr69=)	rs751347311	0.00009
NM_001378969.1(KCND3):c.1348C>T (p.Leu450Phe)	rs150401343	0.00006
NM_001378969.1(KCND3):c.651G>A (p.Pro217=)	rs186974111	0.00006
NM_001378969.1(KCND3):c.1173C>T (p.Gly391=)	rs533201615	0.00004
NM_001378969.1(KCND3):c.1269+18G>A	rs372005674	0.00004
NM_001378969.1(KCND3):c.519C>T (p.Phe173=)	rs144600384	0.00004
NM_001378969.1(KCND3):c.618G>A (p.Pro206=)	rs200611538	0.00004
NM_001378969.1(KCND3):c.1314G>A (p.Ser438=)	rs1247179970	0.00003
NM_001378969.1(KCND3):c.1524C>T (p.His508=)	rs765916708	0.00003
NM_001378969.1(KCND3):c.339C>T (p.Ala113=)	rs371366472	0.00003
NM_001378969.1(KCND3):c.693G>C (p.Thr231=)	rs749849320	0.00003
NM_001378969.1(KCND3):c.1353C>T (p.Asn451=)	rs148320813	0.00002
NM_001378969.1(KCND3):c.1368G>A (p.Leu456=)	rs17215451	0.00002
NM_001378969.1(KCND3):c.1519-5C>T	rs376408039	0.00002
NM_001378969.1(KCND3):c.1752C>A (p.Pro584=)	rs771385731	0.00002
NM_001378969.1(KCND3):c.1794C>T (p.Asp598=)	rs181971539	0.00002
NM_001378969.1(KCND3):c.318G>A (p.Pro106=)	rs770807162	0.00002
NM_001378969.1(KCND3):c.321C>A (p.Arg107=)	rs746952612	0.00002
NM_001378969.1(KCND3):c.348C>T (p.Asp116=)	rs756600533	0.00002
NM_001378969.1(KCND3):c.576C>T (p.Phe192=)	rs759120826	0.00002
NM_001378969.1(KCND3):c.879C>T (p.Arg293=)	rs147739517	0.00002
NM_001378969.1(KCND3):c.9C>T (p.Ala3=)	rs777097802	0.00002
NM_001378969.1(KCND3):c.1146C>A (p.Ile382=)	rs185723423	0.00001
NM_001378969.1(KCND3):c.1359G>A (p.Ala453=)	rs762936059	0.00001
NM_001378969.1(KCND3):c.1362G>A (p.Leu454=)	rs765815341	0.00001
NM_001378969.1(KCND3):c.1372-6T>C	rs765435324	0.00001
NM_001378969.1(KCND3):c.1462-13T>C	rs766769240	0.00001
NM_001378969.1(KCND3):c.1492T>C (p.Leu498=)	rs762528364	0.00001
NM_001378969.1(KCND3):c.1518+18T>C	rs377356478	0.00001
NM_001378969.1(KCND3):c.186G>A (p.Pro62=)	rs1411627342	0.00001
NM_001378969.1(KCND3):c.1917C>A (p.Asn639Lys)	rs777172603	0.00001
NM_001378969.1(KCND3):c.324C>T (p.Tyr108=)	rs777559132	0.00001
NM_001378969.1(KCND3):c.399C>T (p.Tyr133=)	rs144184587	0.00001
NM_001378969.1(KCND3):c.609G>A (p.Glu203=)	rs1171946587	0.00001
NM_001378969.1(KCND3):c.727C>T (p.Leu243=)	rs769885163	0.00001
NM_001378969.1(KCND3):c.837C>T (p.Asn279=)	rs761397595	0.00001
NM_001378969.1(KCND3):c.96C>T (p.Ala32=)	rs767230824	0.00001
NM_001378969.1(KCND3):c.999C>T (p.Ile333=)	rs1250316713	0.00001
NM_001378969.1(KCND3):c.1026C>G (p.Ala342=)	rs1216276887
NM_001378969.1(KCND3):c.1041G>A (p.Ser347=)	rs369361457
NM_001378969.1(KCND3):c.1050G>A (p.Lys350=)
NM_001378969.1(KCND3):c.1053C>T (p.Phe351=)
NM_001378969.1(KCND3):c.1062C>T (p.Ile354=)
NM_001378969.1(KCND3):c.1065T>A (p.Pro355=)	rs1467256846
NM_001378969.1(KCND3):c.1098C>A (p.Thr366=)
NM_001378969.1(KCND3):c.1106+11G>A
NM_001378969.1(KCND3):c.1106+11G>T	rs1437557964
NM_001378969.1(KCND3):c.1107-21_1107-20del
NM_001378969.1(KCND3):c.1131G>A (p.Thr377=)
NM_001378969.1(KCND3):c.1158C>T (p.Ile386=)
NM_001378969.1(KCND3):c.1167G>A (p.Leu389=)	rs1571636426
NM_001378969.1(KCND3):c.1173C>A (p.Gly391=)	rs533201615
NM_001378969.1(KCND3):c.1194A>G (p.Pro398=)
NM_001378969.1(KCND3):c.1197C>T (p.Val399=)
NM_001378969.1(KCND3):c.1269+14G>A	rs369047161
NM_001378969.1(KCND3):c.1270-20dup
NM_001378969.1(KCND3):c.1270-6T>C	rs1195309269
NM_001378969.1(KCND3):c.1305A>T (p.Thr435=)
NM_001378969.1(KCND3):c.1324C>T (p.Leu442=)
NM_001378969.1(KCND3):c.1329C>T (p.His443=)
NM_001378969.1(KCND3):c.1371+19T>G
NM_001378969.1(KCND3):c.1372-14T>C
NM_001378969.1(KCND3):c.1372-17T>C
NM_001378969.1(KCND3):c.1372-4C>T
NM_001378969.1(KCND3):c.1372-6T>G
NM_001378969.1(KCND3):c.1413C>A (p.Leu471=)
NM_001378969.1(KCND3):c.1434C>T (p.His478=)
NM_001378969.1(KCND3):c.1461+7C>A
NM_001378969.1(KCND3):c.1461+9C>T
NM_001378969.1(KCND3):c.1462-10T>G	rs2101462550
NM_001378969.1(KCND3):c.1462-16G>T
NM_001378969.1(KCND3):c.1462-4G>A
NM_001378969.1(KCND3):c.1518+17A>C
NM_001378969.1(KCND3):c.1519-10C>T	rs1664168851
NM_001378969.1(KCND3):c.1519-17_1519-15del
NM_001378969.1(KCND3):c.1519-20_1519-18del	rs775978779
NM_001378969.1(KCND3):c.1536T>C (p.Asp512=)
NM_001378969.1(KCND3):c.1560C>T (p.Cys520=)
NM_001378969.1(KCND3):c.1587A>G (p.Pro529=)
NM_001378969.1(KCND3):c.159C>T (p.Thr53=)
NM_001378969.1(KCND3):c.1641C>T (p.Cys547=)
NM_001378969.1(KCND3):c.1683C>T (p.Asn561=)
NM_001378969.1(KCND3):c.1692T>G (p.Ala564=)
NM_001378969.1(KCND3):c.1701G>A (p.Leu567=)
NM_001378969.1(KCND3):c.1725G>A (p.Thr575=)
NM_001378969.1(KCND3):c.1740C>A (p.Gly580=)
NM_001378969.1(KCND3):c.1743T>C (p.Ser581=)
NM_001378969.1(KCND3):c.1767-17A>C
NM_001378969.1(KCND3):c.1767-4C>G
NM_001378969.1(KCND3):c.1803G>A (p.Leu601=)
NM_001378969.1(KCND3):c.1866G>A (p.Ala622=)
NM_001378969.1(KCND3):c.186G>C (p.Pro62=)
NM_001378969.1(KCND3):c.18G>A (p.Ala6=)
NM_001378969.1(KCND3):c.1920G>A (p.Thr640=)
NM_001378969.1(KCND3):c.1950C>A (p.Val650=)
NM_001378969.1(KCND3):c.36C>T (p.Ala12=)	rs2102000445
NM_001378969.1(KCND3):c.447C>T (p.Asp149=)	rs1553187519
NM_001378969.1(KCND3):c.486G>A (p.Ser162=)
NM_001378969.1(KCND3):c.492C>T (p.Ser164=)	rs1170371506
NM_001378969.1(KCND3):c.522G>A (p.Glu174=)	rs2101997545
NM_001378969.1(KCND3):c.561C>T (p.Tyr187=)
NM_001378969.1(KCND3):c.600C>T (p.Asn200=)	rs1674984825
NM_001378969.1(KCND3):c.633G>A (p.Pro211=)	rs35131566
NM_001378969.1(KCND3):c.660G>A (p.Glu220=)	rs2101996879
NM_001378969.1(KCND3):c.663C>T (p.Arg221=)
NM_001378969.1(KCND3):c.693G>A (p.Thr231=)
NM_001378969.1(KCND3):c.714C>A (p.Thr238=)
NM_001378969.1(KCND3):c.84C>T (p.Pro28=)
NM_001378969.1(KCND3):c.87G>A (p.Leu29=)
NM_001378969.1(KCND3):c.957C>T (p.Ser319=)	rs61733426
NM_001378969.1(KCND3):c.969T>C (p.Phe323=)	rs757012715

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