List of variants in gene SLMAP reported as uncertain significance for Brugada syndrome

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: 178

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HGVS	dbSNP	gnomAD frequency
NM_001377540.1(SLMAP):c.2042A>G (p.Lys681Arg)	rs150439110	0.00028
NM_001377540.1(SLMAP):c.2020+5A>G	rs199881493	0.00017
NM_001377540.1(SLMAP):c.1063G>A (p.Glu355Lys)	rs149548827	0.00015
NM_001377540.1(SLMAP):c.1703A>G (p.Gln568Arg)	rs141727742	0.00015
NM_001377540.1(SLMAP):c.615+6C>T	rs200859030	0.00015
NM_001377540.1(SLMAP):c.787C>G (p.Gln263Glu)	rs765000724	0.00013
NM_001377540.1(SLMAP):c.346+6G>T	rs371736233	0.00010
NM_001377540.1(SLMAP):c.191C>T (p.Thr64Met)	rs149291683	0.00009
NM_001377540.1(SLMAP):c.31C>T (p.Arg11Cys)	rs767298958	0.00007
NM_001377540.1(SLMAP):c.1284A>G (p.Gln428=)	rs1465764372	0.00006
NM_001377540.1(SLMAP):c.1904G>A (p.Arg635Gln)	rs139032332	0.00006
NM_001377540.1(SLMAP):c.2402A>G (p.Gln801Arg)	rs142778041	0.00005
NM_001377540.1(SLMAP):c.1289T>C (p.Ile430Thr)	rs375841302	0.00004
NM_001377540.1(SLMAP):c.1516G>T (p.Ala506Ser)	rs76544609	0.00004
NM_001377540.1(SLMAP):c.198+5T>C	rs759043349	0.00004
NM_001377540.1(SLMAP):c.2431G>C (p.Glu811Gln)	rs751083292	0.00004
NM_001377540.1(SLMAP):c.722T>C (p.Ile241Thr)	rs772627783	0.00004
NM_001377540.1(SLMAP):c.830G>A (p.Arg277Gln)	rs756718350	0.00004
NM_001377540.1(SLMAP):c.1270A>G (p.Thr424Ala)	rs746146243	0.00003
NM_001377540.1(SLMAP):c.1747A>G (p.Lys583Glu)	rs1260232243	0.00003
NM_001377540.1(SLMAP):c.2065G>A (p.Glu689Lys)	rs147989677	0.00003
NM_001377540.1(SLMAP):c.407G>A (p.Arg136Gln)	rs142516364	0.00003
NM_001377540.1(SLMAP):c.710G>A (p.Arg237Gln)	rs767174100	0.00003
NM_001377540.1(SLMAP):c.1312G>A (p.Val438Ile)	rs751946618	0.00002
NM_001377540.1(SLMAP):c.1624+1G>T	rs140490085	0.00002
NM_001377540.1(SLMAP):c.1655G>A (p.Arg552Gln)	rs372758327	0.00002
NM_001377540.1(SLMAP):c.1814A>G (p.His605Arg)	rs746778162	0.00002
NM_001377540.1(SLMAP):c.2189T>A (p.Met730Lys)	rs371314097	0.00002
NM_001377540.1(SLMAP):c.2243G>A (p.Arg748Gln)	rs141277984	0.00002
NM_001377540.1(SLMAP):c.4C>T (p.Pro2Ser)	rs973236515	0.00002
NM_001377540.1(SLMAP):c.646C>T (p.Arg216Trp)	rs367733735	0.00002
NM_001377540.1(SLMAP):c.940A>G (p.Ile314Val)	rs776232087	0.00002
NM_001377540.1(SLMAP):c.*38C>T	rs771357380	0.00001
NM_001377540.1(SLMAP):c.*55G>A	rs1210310709	0.00001
NM_001377540.1(SLMAP):c.1036A>G (p.Ile346Val)	rs945147965	0.00001
NM_001377540.1(SLMAP):c.1048G>A (p.Glu350Lys)	rs1205218778	0.00001
NM_001377540.1(SLMAP):c.1094C>A (p.Ala365Asp)	rs375002159	0.00001
NM_001377540.1(SLMAP):c.1109C>G (p.Thr370Ser)	rs766605023	0.00001
NM_001377540.1(SLMAP):c.1261G>A (p.Gly421Arg)	rs1203771969	0.00001
NM_001377540.1(SLMAP):c.1271C>T (p.Thr424Ile)	rs1423544190	0.00001
NM_001377540.1(SLMAP):c.1300+4A>G	rs1317261965	0.00001
NM_001377540.1(SLMAP):c.1334C>T (p.Ala445Val)	rs757740736	0.00001
NM_001377540.1(SLMAP):c.1354T>C (p.Ser452Pro)	rs373548009	0.00001
NM_001377540.1(SLMAP):c.1390T>A (p.Phe464Ile)	rs772143236	0.00001
NM_001377540.1(SLMAP):c.1690G>A (p.Val564Ile)	rs570222284	0.00001
NM_001377540.1(SLMAP):c.1700-5T>C	rs1056223038	0.00001
NM_001377540.1(SLMAP):c.1810C>T (p.Leu604Phe)	rs777679999	0.00001
NM_001377540.1(SLMAP):c.1843C>T (p.Arg615Trp)	rs1379169914	0.00001
NM_001377540.1(SLMAP):c.1919C>T (p.Ala640Val)	rs762174645	0.00001
NM_001377540.1(SLMAP):c.2117G>A (p.Arg706Gln)	rs762620820	0.00001
NM_001377540.1(SLMAP):c.2167A>G (p.Ser723Gly)	rs764100894	0.00001
NM_001377540.1(SLMAP):c.2213A>T (p.Gln738Leu)	rs754097857	0.00001
NM_001377540.1(SLMAP):c.2235G>C (p.Gln745His)	rs758343458	0.00001
NM_001377540.1(SLMAP):c.2286C>A (p.Asn762Lys)	rs975284095	0.00001
NM_001377540.1(SLMAP):c.2394G>T (p.Glu798Asp)	rs750893840	0.00001
NM_001377540.1(SLMAP):c.304A>G (p.Ile102Val)	rs756212703	0.00001
NM_001377540.1(SLMAP):c.346+4C>T	rs201859602	0.00001
NM_001377540.1(SLMAP):c.412C>T (p.Arg138Cys)	rs748820617	0.00001
NM_001377540.1(SLMAP):c.480G>C (p.Met160Ile)	rs770086716	0.00001
NM_001377540.1(SLMAP):c.519+6A>C	rs2094439140	0.00001
NM_001377540.1(SLMAP):c.532C>T (p.Arg178Trp)	rs766644866	0.00001
NM_001377540.1(SLMAP):c.563C>T (p.Thr188Met)	rs763740777	0.00001
NM_001377540.1(SLMAP):c.572G>A (p.Arg191Gln)	rs756779633	0.00001
NM_001377540.1(SLMAP):c.723A>G (p.Ile241Met)	rs760182153	0.00001
NM_001377540.1(SLMAP):c.824T>C (p.Val275Ala)	rs138336324	0.00001
NM_001377540.1(SLMAP):c.880G>A (p.Glu294Lys)	rs770596419	0.00001
NC_000003.11:g.(?_57743379)_(57817277_?)dup
NC_000003.11:g.(?_57847666)_(57847823_?)dup
NC_000003.11:g.(?_57893591)_(57893753_?)del
NM_001377540.1(SLMAP):c.*37G>A
NM_001377540.1(SLMAP):c.*70G>A
NM_001377540.1(SLMAP):c.*94C>G
NM_001377540.1(SLMAP):c.1009G>A (p.Ala337Thr)
NM_001377540.1(SLMAP):c.1012G>C (p.Glu338Gln)	rs2153604748
NM_001377540.1(SLMAP):c.1084G>T (p.Ala362Ser)
NM_001377540.1(SLMAP):c.1105T>G (p.Phe369Val)
NM_001377540.1(SLMAP):c.1112A>G (p.Asn371Ser)
NM_001377540.1(SLMAP):c.1131_1132delinsCA (p.Leu377_Gln378delinsPheLys)	rs1577969548
NM_001377540.1(SLMAP):c.1135+6T>G
NM_001377540.1(SLMAP):c.113G>T (p.Arg38Leu)
NM_001377540.1(SLMAP):c.119C>T (p.Ala40Val)	rs1228536991
NM_001377540.1(SLMAP):c.1238-9_1238-6del
NM_001377540.1(SLMAP):c.1249T>G (p.Ser417Ala)	rs2095481948
NM_001377540.1(SLMAP):c.1258G>A (p.Gly420Ser)
NM_001377540.1(SLMAP):c.1260C>T (p.Gly420=)
NM_001377540.1(SLMAP):c.1301-7T>G
NM_001377540.1(SLMAP):c.1315G>A (p.Glu439Lys)	rs747337211
NM_001377540.1(SLMAP):c.1315G>C (p.Glu439Gln)
NM_001377540.1(SLMAP):c.1337T>C (p.Val446Ala)
NM_001377540.1(SLMAP):c.1343A>G (p.Glu448Gly)	rs755917730
NM_001377540.1(SLMAP):c.1368G>T (p.Gln456His)
NM_001377540.1(SLMAP):c.1382A>C (p.Glu461Ala)	rs901233405
NM_001377540.1(SLMAP):c.1429G>A (p.Asp477Asn)
NM_001377540.1(SLMAP):c.1432G>A (p.Asp478Asn)	rs1016820088
NM_001377540.1(SLMAP):c.1435A>G (p.Thr479Ala)
NM_001377540.1(SLMAP):c.1440A>C (p.Thr480=)
NM_001377540.1(SLMAP):c.1442-3T>C
NM_001377540.1(SLMAP):c.1462G>T (p.Asp488Tyr)
NM_001377540.1(SLMAP):c.1477C>T (p.Leu493Phe)
NM_001377540.1(SLMAP):c.1483A>C (p.Lys495Gln)
NM_001377540.1(SLMAP):c.1501+1del	rs1446668420
NM_001377540.1(SLMAP):c.1501+4C>T	rs539985706
NM_001377540.1(SLMAP):c.1528A>G (p.Ile510Val)	rs2096607019
NM_001377540.1(SLMAP):c.1559G>A (p.Arg520Gln)	rs765688735
NM_001377540.1(SLMAP):c.1569G>T (p.Leu523Phe)
NM_001377540.1(SLMAP):c.1580A>C (p.Gln527Pro)
NM_001377540.1(SLMAP):c.1686A>G (p.Ile562Met)	rs2096633047
NM_001377540.1(SLMAP):c.1693C>G (p.Leu565Val)
NM_001377540.1(SLMAP):c.1699+4T>G
NM_001377540.1(SLMAP):c.1720A>G (p.Ile574Val)
NM_001377540.1(SLMAP):c.1723G>A (p.Asp575Asn)
NM_001377540.1(SLMAP):c.1739G>A (p.Arg580Gln)	rs138744399
NM_001377540.1(SLMAP):c.1747_1749del (p.Lys583del)
NM_001377540.1(SLMAP):c.1753A>C (p.Ser585Arg)	rs370779290
NM_001377540.1(SLMAP):c.1784T>C (p.Leu595Pro)
NM_001377540.1(SLMAP):c.1790C>T (p.Ala597Val)
NM_001377540.1(SLMAP):c.1806G>T (p.Leu602Phe)
NM_001377540.1(SLMAP):c.1831G>T (p.Val611Phe)
NM_001377540.1(SLMAP):c.1844G>A (p.Arg615Gln)
NM_001377540.1(SLMAP):c.1872A>C (p.Glu624Asp)
NM_001377540.1(SLMAP):c.1896G>T (p.Glu632Asp)
NM_001377540.1(SLMAP):c.1910G>A (p.Arg637Gln)
NM_001377540.1(SLMAP):c.1916C>T (p.Ala639Val)
NM_001377540.1(SLMAP):c.1988A>T (p.Asp663Val)	rs140982905
NM_001377540.1(SLMAP):c.1992G>T (p.Gln664His)
NM_001377540.1(SLMAP):c.1997G>A (p.Arg666Lys)
NM_001377540.1(SLMAP):c.205C>A (p.Leu69Ile)
NM_001377540.1(SLMAP):c.211G>T (p.Asp71Tyr)	rs2093330967
NM_001377540.1(SLMAP):c.2123A>G (p.Glu708Gly)
NM_001377540.1(SLMAP):c.2137A>G (p.Asn713Asp)
NM_001377540.1(SLMAP):c.2141C>A (p.Ser714Tyr)
NM_001377540.1(SLMAP):c.2145G>C (p.Gln715His)
NM_001377540.1(SLMAP):c.2180T>C (p.Ile727Thr)
NM_001377540.1(SLMAP):c.2182C>T (p.Leu728Phe)	rs2153698213
NM_001377540.1(SLMAP):c.2190G>A (p.Met730Ile)
NM_001377540.1(SLMAP):c.2312A>G (p.Tyr771Cys)
NM_001377540.1(SLMAP):c.2353T>C (p.Phe785Leu)
NM_001377540.1(SLMAP):c.2357A>G (p.Glu786Gly)
NM_001377540.1(SLMAP):c.2361G>T (p.Met787Ile)
NM_001377540.1(SLMAP):c.2362A>T (p.Thr788Ser)
NM_001377540.1(SLMAP):c.238A>G (p.Ile80Val)	rs901486021
NM_001377540.1(SLMAP):c.2429G>A (p.Arg810Gln)
NM_001377540.1(SLMAP):c.2437G>A (p.Gly813Arg)	rs1444785203
NM_001377540.1(SLMAP):c.2440A>G (p.Asn814Asp)	rs1214562198
NM_001377540.1(SLMAP):c.2441A>G (p.Asn814Ser)
NM_001377540.1(SLMAP):c.258T>G (p.Ser86Arg)	rs2093332186
NM_001377540.1(SLMAP):c.265T>G (p.Ser89Ala)	rs2153547258
NM_001377540.1(SLMAP):c.275G>A (p.Ser92Asn)
NM_001377540.1(SLMAP):c.346+5G>A	rs2093334864
NM_001377540.1(SLMAP):c.347-1G>T	rs1060503190
NM_001377540.1(SLMAP):c.413G>C (p.Arg138Pro)
NM_001377540.1(SLMAP):c.419+3G>A
NM_001377540.1(SLMAP):c.421G>A (p.Val141Ile)
NM_001377540.1(SLMAP):c.436_441del (p.Leu146_Pro147del)
NM_001377540.1(SLMAP):c.440C>G (p.Pro147Arg)
NM_001377540.1(SLMAP):c.473C>T (p.Pro158Leu)
NM_001377540.1(SLMAP):c.482A>C (p.Tyr161Ser)
NM_001377540.1(SLMAP):c.563C>A (p.Thr188Lys)
NM_001377540.1(SLMAP):c.626A>G (p.Asp209Gly)
NM_001377540.1(SLMAP):c.652G>A (p.Glu218Lys)	rs1577820022
NM_001377540.1(SLMAP):c.655G>C (p.Val219Leu)
NM_001377540.1(SLMAP):c.703A>G (p.Ser235Gly)	rs774215191
NM_001377540.1(SLMAP):c.732del (p.Glu245fs)
NM_001377540.1(SLMAP):c.776G>A (p.Arg259Lys)	rs2153599158
NM_001377540.1(SLMAP):c.790G>C (p.Glu264Gln)	rs2153599173
NM_001377540.1(SLMAP):c.809G>C (p.Arg270Thr)
NM_001377540.1(SLMAP):c.820G>C (p.Glu274Gln)
NM_001377540.1(SLMAP):c.826G>A (p.Glu276Lys)
NM_001377540.1(SLMAP):c.832A>G (p.Ser278Gly)
NM_001377540.1(SLMAP):c.852T>G (p.Asp284Glu)	rs2153600640
NM_001377540.1(SLMAP):c.875T>C (p.Met292Thr)
NM_001377540.1(SLMAP):c.878A>G (p.Asn293Ser)
NM_001377540.1(SLMAP):c.928G>A (p.Ala310Thr)	rs754387957
NM_001377540.1(SLMAP):c.929C>T (p.Ala310Val)
NM_001377540.1(SLMAP):c.937G>A (p.Glu313Lys)
NM_001377540.1(SLMAP):c.941T>G (p.Ile314Ser)	rs779312973
NM_001377540.1(SLMAP):c.966+4T>A	rs2095093240
NM_001377540.1(SLMAP):c.990A>T (p.Glu330Asp)

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