List of variants in gene combination CHAT, SLC18A3 reported as likely benign for not provided

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: 98

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HGVS	dbSNP	gnomAD frequency
NM_003055.3(SLC18A3):c.85C>T (p.Arg29Trp)	rs8187734	0.00207
NM_003055.3(SLC18A3):c.32G>A (p.Arg11Gln)	rs8187732	0.00062
NM_003055.3(SLC18A3):c.208G>A (p.Gly70Ser)	rs758567871	0.00030
NM_003055.3(SLC18A3):c.1035C>G (p.Thr345=)	rs138830933	0.00016
NM_003055.3(SLC18A3):c.825C>T (p.Asn275=)	rs145315435	0.00016
NM_003055.3(SLC18A3):c.1479G>A (p.Leu493=)	rs376281494	0.00015
NM_003055.3(SLC18A3):c.1030C>G (p.Leu344Val)	rs78571038	0.00014
NM_003055.3(SLC18A3):c.924C>A (p.Leu308=)	rs200094927	0.00010
NM_003055.3(SLC18A3):c.1500T>C (p.Arg500=)	rs200368763	0.00006
NM_003055.3(SLC18A3):c.915C>A (p.Leu305=)	rs8187728	0.00006
NM_003055.3(SLC18A3):c.687G>T (p.Pro229=)	rs755075120	0.00004
NM_003055.3(SLC18A3):c.1453C>T (p.Leu485=)	rs376743590	0.00002
NM_003055.3(SLC18A3):c.1455G>A (p.Leu485=)	rs751093639	0.00002
NM_003055.3(SLC18A3):c.510C>A (p.Ala170=)	rs750306476	0.00002
NM_003055.3(SLC18A3):c.543G>T (p.Ala181=)	rs745946207	0.00002
NM_003055.3(SLC18A3):c.1143G>T (p.Ala381=)	rs777864075	0.00001
NM_003055.3(SLC18A3):c.1206G>T (p.Leu402=)	rs1838309883	0.00001
NM_003055.3(SLC18A3):c.1302C>G (p.Leu434=)	rs748705960	0.00001
NM_003055.3(SLC18A3):c.1308C>T (p.Pro436=)	rs1838313296	0.00001
NM_003055.3(SLC18A3):c.261G>A (p.Pro87=)	rs773239597	0.00001
NM_003055.3(SLC18A3):c.393G>A (p.Lys131=)	rs757816248	0.00001
NM_003055.3(SLC18A3):c.525C>T (p.Tyr175=)	rs375171478	0.00001
NM_003055.3(SLC18A3):c.534G>A (p.Leu178=)	rs749642076	0.00001
NM_003055.3(SLC18A3):c.642G>A (p.Leu214=)	rs759417045	0.00001
NM_003055.3(SLC18A3):c.651G>A (p.Ala217=)	rs760191637	0.00001
NM_003055.3(SLC18A3):c.708T>C (p.Tyr236=)	rs1270083337	0.00001
NM_003055.3(SLC18A3):c.855C>T (p.Leu285=)	rs551042891	0.00001
NM_003055.3(SLC18A3):c.999G>A (p.Pro333=)	rs1323911631	0.00001
NM_003055.3(SLC18A3):c.1044G>A (p.Leu348=)	rs1404084769
NM_003055.3(SLC18A3):c.1063C>T (p.Leu355=)
NM_003055.3(SLC18A3):c.1074G>A (p.Leu358=)
NM_003055.3(SLC18A3):c.1083G>T (p.Ala361=)
NM_003055.3(SLC18A3):c.108T>A (p.Leu36=)
NM_003055.3(SLC18A3):c.1092G>C (p.Leu364=)
NM_003055.3(SLC18A3):c.1101C>T (p.Ile367=)	rs2132688096
NM_003055.3(SLC18A3):c.1113G>T (p.Ser371=)	rs1360779629
NM_003055.3(SLC18A3):c.1122G>C (p.Val374=)
NM_003055.3(SLC18A3):c.114C>T (p.Ile38=)
NM_003055.3(SLC18A3):c.1155C>T (p.Val385=)
NM_003055.3(SLC18A3):c.1164C>T (p.Cys388=)
NM_003055.3(SLC18A3):c.1185C>A (p.Ala395=)	rs1215490692
NM_003055.3(SLC18A3):c.1185C>T (p.Ala395=)	rs1215490692
NM_003055.3(SLC18A3):c.1200A>T (p.Ala400=)	rs1243378683
NM_003055.3(SLC18A3):c.1212G>T (p.Thr404=)
NM_003055.3(SLC18A3):c.1215C>T (p.Leu405=)
NM_003055.3(SLC18A3):c.1230C>T (p.Asp410=)
NM_003055.3(SLC18A3):c.1248C>G (p.Val416=)
NM_003055.3(SLC18A3):c.1251T>C (p.Tyr417=)
NM_003055.3(SLC18A3):c.1293C>T (p.Ala431=)	rs1838312632
NM_003055.3(SLC18A3):c.1296C>T (p.Tyr432=)
NM_003055.3(SLC18A3):c.1299G>C (p.Ala433=)
NM_003055.3(SLC18A3):c.1299G>T (p.Ala433=)
NM_003055.3(SLC18A3):c.12G>A (p.Ala4=)
NM_003055.3(SLC18A3):c.1302C>A (p.Leu434=)
NM_003055.3(SLC18A3):c.1329G>A (p.Val443=)	rs2132688687
NM_003055.3(SLC18A3):c.1392C>G (p.Pro464=)
NM_003055.3(SLC18A3):c.1461T>C (p.Asp487=)	rs974690319
NM_003055.3(SLC18A3):c.1542G>C (p.Pro514=)	rs1045968094
NM_003055.3(SLC18A3):c.1551T>G (p.Pro517=)	rs2132689381
NM_003055.3(SLC18A3):c.1591C>T (p.Arg531Cys)	rs148062083
NM_003055.3(SLC18A3):c.183C>T (p.Ile61=)
NM_003055.3(SLC18A3):c.195C>T (p.Arg65=)
NM_003055.3(SLC18A3):c.216C>A (p.Thr72=)	rs1235546648
NM_003055.3(SLC18A3):c.225C>T (p.Pro75=)
NM_003055.3(SLC18A3):c.240C>T (p.Pro80=)	rs2132685994
NM_003055.3(SLC18A3):c.244C>T (p.Leu82=)
NM_003055.3(SLC18A3):c.249G>A (p.Pro83=)
NM_003055.3(SLC18A3):c.249G>T (p.Pro83=)	rs150436609
NM_003055.3(SLC18A3):c.288C>T (p.Asn96=)
NM_003055.3(SLC18A3):c.318A>G (p.Pro106=)
NM_003055.3(SLC18A3):c.351G>A (p.Thr117=)	rs1258093533
NM_003055.3(SLC18A3):c.36G>A (p.Ala12=)
NM_003055.3(SLC18A3):c.379C>T (p.Leu127=)
NM_003055.3(SLC18A3):c.39G>A (p.Ala13=)
NM_003055.3(SLC18A3):c.513C>T (p.Phe171=)
NM_003055.3(SLC18A3):c.519G>A (p.Glu173=)
NM_003055.3(SLC18A3):c.534G>C (p.Leu178=)	rs749642076
NM_003055.3(SLC18A3):c.570C>T (p.Ala190=)
NM_003055.3(SLC18A3):c.600C>T (p.Ile200=)
NM_003055.3(SLC18A3):c.603C>G (p.Ala201=)	rs148566667
NM_003055.3(SLC18A3):c.669C>T (p.Phe223=)
NM_003055.3(SLC18A3):c.717C>T (p.Ala239=)
NM_003055.3(SLC18A3):c.741G>T (p.Val247=)
NM_003055.3(SLC18A3):c.765C>T (p.Asp255=)
NM_003055.3(SLC18A3):c.768G>A (p.Ala256=)
NM_003055.3(SLC18A3):c.769C>T (p.Leu257=)
NM_003055.3(SLC18A3):c.811C>A (p.Arg271=)
NM_003055.3(SLC18A3):c.816T>A (p.Ala272=)	rs2132687364
NM_003055.3(SLC18A3):c.840T>A (p.Thr280=)
NM_003055.3(SLC18A3):c.843C>G (p.Pro281=)
NM_003055.3(SLC18A3):c.861A>G (p.Leu287=)	rs1564466482
NM_003055.3(SLC18A3):c.864C>T (p.Asp288=)
NM_003055.3(SLC18A3):c.867C>T (p.Pro289=)
NM_003055.3(SLC18A3):c.90G>A (p.Arg30=)	rs140489850
NM_003055.3(SLC18A3):c.915C>T (p.Leu305=)	rs8187728
NM_003055.3(SLC18A3):c.957G>A (p.Thr319=)
NM_003055.3(SLC18A3):c.972G>A (p.Glu324=)
NM_003055.3(SLC18A3):c.9C>T (p.Ser3=)

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