ClinVar Miner

List of variants in gene SYN1 reported as likely benign for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 172
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HGVS dbSNP gnomAD frequency
NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala) rs200533370 0.01462
NM_006950.3(SYN1):c.1325T>C (p.Leu442Pro) rs375440874 0.00058
NM_006950.3(SYN1):c.1615G>A (p.Gly539Ser) rs794727076 0.00058
NM_006950.3(SYN1):c.1701A>T (p.Thr567=) rs770195822 0.00046
NM_006950.3(SYN1):c.1063C>T (p.Leu355=) rs191822319 0.00025
NM_006950.3(SYN1):c.1569G>A (p.Ala523=) rs587781185 0.00022
NM_006950.3(SYN1):c.939C>T (p.Asp313=) rs373928763 0.00020
NM_006950.3(SYN1):c.1968G>A (p.Pro656=) rs199844514 0.00018
NM_006950.3(SYN1):c.1369G>C (p.Ala457Pro) rs748323076 0.00017
NM_006950.3(SYN1):c.319G>A (p.Gly107Ser) rs765045862 0.00012
NM_006950.3(SYN1):c.1158+17G>T rs769125543 0.00010
NM_006950.3(SYN1):c.987G>A (p.Thr329=) rs371126022 0.00008
NM_006950.3(SYN1):c.564C>T (p.His188=) rs768956462 0.00007
NM_006950.3(SYN1):c.1137C>T (p.Asp379=) rs762471804 0.00006
NM_006950.3(SYN1):c.249G>T (p.Ala83=) rs780753887 0.00006
NM_006950.3(SYN1):c.436-12T>C rs1057120503 0.00006
NM_006950.3(SYN1):c.897G>A (p.Lys299=) rs142297702 0.00006
NM_006950.3(SYN1):c.1026G>A (p.Ala342=) rs777301855 0.00005
NM_006950.3(SYN1):c.108T>C (p.Gly36=) rs758180955 0.00005
NM_006950.3(SYN1):c.360C>A (p.Asp120Glu) rs372165835 0.00005
NM_006950.3(SYN1):c.720G>A (p.Gly240=) rs149166420 0.00005
NM_006950.3(SYN1):c.1065G>A (p.Leu355=) rs1410566216 0.00004
NM_006950.3(SYN1):c.1263G>A (p.Gln421=) rs746903128 0.00004
NM_006950.3(SYN1):c.1692C>T (p.Thr564=) rs1463522576 0.00004
NM_006950.3(SYN1):c.435+10G>A rs771547188 0.00004
NM_006950.3(SYN1):c.630C>T (p.Ile210=) rs35944641 0.00004
NM_006950.3(SYN1):c.540G>A (p.Pro180=) rs769771865 0.00003
NM_006950.3(SYN1):c.585C>T (p.Asn195=) rs746025499 0.00003
NM_006950.3(SYN1):c.678C>T (p.Pro226=) rs1331758208 0.00003
NM_006950.3(SYN1):c.838-12G>A rs373591101 0.00003
NM_006950.3(SYN1):c.1122G>A (p.Ala374=) rs757867825 0.00002
NM_006950.3(SYN1):c.1159-4C>T rs897051260 0.00002
NM_006950.3(SYN1):c.1179G>A (p.Pro393=) rs1471942298 0.00002
NM_006950.3(SYN1):c.1251C>A (p.Ala417=) rs765003722 0.00002
NM_006950.3(SYN1):c.1305+13G>C rs749347824 0.00002
NM_006950.3(SYN1):c.1356C>T (p.Pro452=) rs749470625 0.00002
NM_006950.3(SYN1):c.1362G>A (p.Gly454=) rs778151348 0.00002
NM_006950.3(SYN1):c.1971C>T (p.His657=) rs201236500 0.00002
NM_006950.3(SYN1):c.646T>C (p.Leu216=) rs1386366470 0.00002
NM_006950.3(SYN1):c.1159-7C>T rs767722750 0.00001
NM_006950.3(SYN1):c.1394-7C>T rs1411087897 0.00001
NM_006950.3(SYN1):c.1425G>A (p.Gln475=) rs1372197618 0.00001
NM_006950.3(SYN1):c.1455G>A (p.Pro485=) rs1302222032 0.00001
NM_006950.3(SYN1):c.1578C>G (p.Thr526=) rs367796785 0.00001
NM_006950.3(SYN1):c.1737G>T (p.Gly579=) rs1290669980 0.00001
NM_006950.3(SYN1):c.1818G>A (p.Gln606=) rs967215240 0.00001
NM_006950.3(SYN1):c.213G>A (p.Ser71=) rs774873821 0.00001
NM_006950.3(SYN1):c.438C>T (p.Ala146=) rs1445481586 0.00001
NM_006950.3(SYN1):c.513G>A (p.Gly171=) rs758981794 0.00001
NM_006950.3(SYN1):c.738A>G (p.Leu246=) rs184905398 0.00001
NM_006950.3(SYN1):c.84G>T (p.Pro28=) rs1197131143 0.00001
NM_006950.3(SYN1):c.102G>A (p.Pro34=)
NM_006950.3(SYN1):c.1055+11C>T
NM_006950.3(SYN1):c.1055+17C>G
NM_006950.3(SYN1):c.1055+9C>T
NM_006950.3(SYN1):c.1056-20C>T
NM_006950.3(SYN1):c.1077G>A (p.Thr359=)
NM_006950.3(SYN1):c.1134G>A (p.Lys378=)
NM_006950.3(SYN1):c.1149C>T (p.His383=)
NM_006950.3(SYN1):c.1158+15G>T
NM_006950.3(SYN1):c.1158+16G>A
NM_006950.3(SYN1):c.1159-10C>T
NM_006950.3(SYN1):c.1159-20G>A rs1045349354
NM_006950.3(SYN1):c.117C>T (p.Ser39=)
NM_006950.3(SYN1):c.120C>T (p.Pro40=)
NM_006950.3(SYN1):c.1215C>A (p.Leu405=)
NM_006950.3(SYN1):c.1218C>T (p.Ile406=)
NM_006950.3(SYN1):c.1227C>A (p.Leu409=) rs1603051010
NM_006950.3(SYN1):c.1227C>T (p.Leu409=) rs1603051010
NM_006950.3(SYN1):c.1236C>T (p.Asn412=)
NM_006950.3(SYN1):c.1239G>A (p.Lys413=)
NM_006950.3(SYN1):c.1264C>A (p.Arg422=) rs757027813
NM_006950.3(SYN1):c.1305+14C>T
NM_006950.3(SYN1):c.1305+18G>A
NM_006950.3(SYN1):c.1306-18T>C
NM_006950.3(SYN1):c.1306-5C>T
NM_006950.3(SYN1):c.1306-6C>T
NM_006950.3(SYN1):c.1306-9C>T rs1603050792
NM_006950.3(SYN1):c.1326G>A (p.Leu442=)
NM_006950.3(SYN1):c.132C>T (p.Pro44=)
NM_006950.3(SYN1):c.1335C>T (p.Gly445=) rs2147912475
NM_006950.3(SYN1):c.1338C>T (p.Arg446=)
NM_006950.3(SYN1):c.1371T>C (p.Ala457=)
NM_006950.3(SYN1):c.1374G>A (p.Gln458=)
NM_006950.3(SYN1):c.1380A>T (p.Arg460=) rs2147912444
NM_006950.3(SYN1):c.1383C>A (p.Pro461=)
NM_006950.3(SYN1):c.1389A>C (p.Pro463=) rs1435656023
NM_006950.3(SYN1):c.1389A>G (p.Pro463=)
NM_006950.3(SYN1):c.1394-10T>G rs1603050623
NM_006950.3(SYN1):c.1394-13C>T
NM_006950.3(SYN1):c.1398C>T (p.Gly466=)
NM_006950.3(SYN1):c.1404A>C (p.Pro468=)
NM_006950.3(SYN1):c.1410G>A (p.Pro470=)
NM_006950.3(SYN1):c.141G>C (p.Gly47=) rs2057941844
NM_006950.3(SYN1):c.141G>T (p.Gly47=)
NM_006950.3(SYN1):c.1470GCA[1] (p.Gln491del) rs775858141
NM_006950.3(SYN1):c.150T>G (p.Thr50=) rs1556861816
NM_006950.3(SYN1):c.1513C>T (p.Pro505Ser)
NM_006950.3(SYN1):c.1525C>T (p.Pro509Ser)
NM_006950.3(SYN1):c.1554C>T (p.Pro518=)
NM_006950.3(SYN1):c.1557G>A (p.Ala519=)
NM_006950.3(SYN1):c.1557G>T (p.Ala519=)
NM_006950.3(SYN1):c.1589G>A (p.Gly530Asp)
NM_006950.3(SYN1):c.1611G>A (p.Ala537=) rs2147912259
NM_006950.3(SYN1):c.1614A>T (p.Gly538=)
NM_006950.3(SYN1):c.1629T>C (p.Pro543=) rs1027134708
NM_006950.3(SYN1):c.1647C>T (p.Pro549=)
NM_006950.3(SYN1):c.1677C>G (p.Gly559=) rs2147912166
NM_006950.3(SYN1):c.1677C>T (p.Gly559=) rs2147912166
NM_006950.3(SYN1):c.1680C>A (p.Pro560=)
NM_006950.3(SYN1):c.1683A>G (p.Pro561=) rs2147912160
NM_006950.3(SYN1):c.168G>C (p.Gly56=)
NM_006950.3(SYN1):c.1704C>G (p.Ser568=)
NM_006950.3(SYN1):c.1731C>T (p.Ala577=) rs2147912133
NM_006950.3(SYN1):c.1764G>A (p.Gln588=)
NM_006950.3(SYN1):c.1782C>T (p.Pro594=) rs2147912100
NM_006950.3(SYN1):c.1791A>G (p.Pro597=)
NM_006950.3(SYN1):c.1794C>G (p.Ala598=) rs2057769499
NM_006950.3(SYN1):c.1815C>T (p.Ser605=) rs1452773137
NM_006950.3(SYN1):c.1821G>A (p.Ala607=)
NM_006950.3(SYN1):c.1851C>A (p.Thr617=) rs2147912062
NM_006950.3(SYN1):c.1869C>T (p.Pro623=)
NM_006950.3(SYN1):c.1884C>T (p.Pro628=) rs2147912043
NM_006950.3(SYN1):c.189G>A (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.189G>T (p.Pro63=) rs371739376
NM_006950.3(SYN1):c.1944C>T (p.Ala648=) rs1556857414
NM_006950.3(SYN1):c.1947C>A (p.Thr649=)
NM_006950.3(SYN1):c.1950C>T (p.Ala650=)
NM_006950.3(SYN1):c.1959G>A (p.Gly653=) rs2147911994
NM_006950.3(SYN1):c.1982+10C>A rs752321936
NM_006950.3(SYN1):c.1982+8_1982+20delinsT
NM_006950.3(SYN1):c.1982+9_1982+20del
NM_006950.3(SYN1):c.249G>A (p.Ala83=) rs780753887
NM_006950.3(SYN1):c.255G>A (p.Lys85=) rs2147933415
NM_006950.3(SYN1):c.303C>T (p.Gly101=) rs1603078601
NM_006950.3(SYN1):c.351G>T (p.Leu117=)
NM_006950.3(SYN1):c.378-14T>C
NM_006950.3(SYN1):c.378-16T>C
NM_006950.3(SYN1):c.378-18G>A
NM_006950.3(SYN1):c.378-19T>A
NM_006950.3(SYN1):c.381A>G (p.Ala127=)
NM_006950.3(SYN1):c.432A>G (p.Glu144=) rs1142635
NM_006950.3(SYN1):c.436-4C>G rs1603071933
NM_006950.3(SYN1):c.441A>G (p.Glu147=)
NM_006950.3(SYN1):c.462G>C (p.Val154=)
NM_006950.3(SYN1):c.527+11G>T
NM_006950.3(SYN1):c.527+18A>G rs2147928548
NM_006950.3(SYN1):c.527+9A>T rs2147928550
NM_006950.3(SYN1):c.528-12C>T
NM_006950.3(SYN1):c.54A>G (p.Pro18=)
NM_006950.3(SYN1):c.579A>G (p.Ala193=) rs1556860653
NM_006950.3(SYN1):c.645C>A (p.Ser215=) rs1299304892
NM_006950.3(SYN1):c.645C>T (p.Ser215=)
NM_006950.3(SYN1):c.684+13A>C
NM_006950.3(SYN1):c.684+16G>A
NM_006950.3(SYN1):c.684+17G>T
NM_006950.3(SYN1):c.685-4A>G rs2147927610
NM_006950.3(SYN1):c.726A>G (p.Glu242=)
NM_006950.3(SYN1):c.744T>C (p.Asp248=)
NM_006950.3(SYN1):c.756C>T (p.Tyr252=) rs1556860614
NM_006950.3(SYN1):c.759C>G (p.Pro253=) rs2147927565
NM_006950.3(SYN1):c.759C>T (p.Pro253=) rs2147927565
NM_006950.3(SYN1):c.837+15G>A
NM_006950.3(SYN1):c.837+19T>C
NM_006950.3(SYN1):c.838-13C>T
NM_006950.3(SYN1):c.84G>A (p.Pro28=)
NM_006950.3(SYN1):c.873C>T (p.Ile291=)
NM_006950.3(SYN1):c.891G>A (p.Leu297=) rs2147913391
NM_006950.3(SYN1):c.900G>A (p.Thr300=)
NM_006950.3(SYN1):c.90G>T (p.Pro30=) rs2147933536
NM_006950.3(SYN1):c.924C>T (p.Ile308=)
NM_006950.3(SYN1):c.945T>C (p.Arg315=)

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