ClinVar Miner

List of variants reported as likely benign for Brugada syndrome 5

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 129
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HGVS dbSNP gnomAD frequency
NM_001037.5(SCN1B):c.591-14C>A rs28365109 0.00920
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027 0.00249
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982 0.00232
NM_001037.5(SCN1B):c.448+321G>A rs72558028 0.00173
NM_001037.5(SCN1B):c.588T>C (p.Asn196=) rs77244433 0.00117
NM_001037.5(SCN1B):c.448+320C>T rs570257058 0.00033
NM_001037.5(SCN1B):c.348G>A (p.Ser116=) rs375050816 0.00021
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582 0.00021
NM_001037.5(SCN1B):c.207+7G>A rs374588869 0.00016
NM_001037.5(SCN1B):c.471C>T (p.Ile157=) rs765269835 0.00014
NM_001037.5(SCN1B):c.96T>C (p.Tyr32=) rs143453040 0.00008
NM_001037.5(SCN1B):c.448+8G>C rs200222933 0.00006
NM_001037.5(SCN1B):c.566C>T (p.Thr189Met) rs2305748 0.00006
NM_001037.5(SCN1B):c.448+140G>A rs775648401 0.00005
NM_001037.5(SCN1B):c.208-14C>T rs72550272 0.00004
NM_001037.5(SCN1B):c.258C>T (p.Phe86=) rs751009774 0.00004
NM_001037.5(SCN1B):c.448+299A>G rs1027861663 0.00004
NM_001037.5(SCN1B):c.448+48A>C rs757515975 0.00004
NM_001037.5(SCN1B):c.366C>T (p.His122=) rs761207251 0.00003
NM_001037.5(SCN1B):c.414C>T (p.Val138=) rs757116018 0.00003
NM_001037.5(SCN1B):c.448+219C>G rs754870200 0.00003
NM_001037.5(SCN1B):c.448+257G>C rs1040023313 0.00003
NM_001037.5(SCN1B):c.448+308C>A rs986180682 0.00003
NM_001037.5(SCN1B):c.448+311G>A rs1019053238 0.00003
NM_001037.5(SCN1B):c.591-5C>T rs1555721514 0.00003
NM_001037.5(SCN1B):c.90C>T (p.Ala30=) rs753994622 0.00003
NM_001037.5(SCN1B):c.408C>T (p.Thr136=) rs200126026 0.00002
NM_001037.5(SCN1B):c.546C>T (p.Tyr182=) rs775659068 0.00002
NM_001037.5(SCN1B):c.63C>T (p.Cys21=) rs200339565 0.00002
NM_001037.5(SCN1B):c.84C>T (p.Thr28=) rs147616219 0.00002
NM_001037.5(SCN1B):c.141C>T (p.Ser47=) rs769535020 0.00001
NM_001037.5(SCN1B):c.150C>T (p.Asn50=) rs147073518 0.00001
NM_001037.5(SCN1B):c.165C>T (p.Thr55=) rs768325106 0.00001
NM_001037.5(SCN1B):c.249T>C (p.Asp83=) rs1234271758 0.00001
NM_001037.5(SCN1B):c.273G>A (p.Val91=) rs16969926 0.00001
NM_001037.5(SCN1B):c.357C>T (p.Tyr119=) rs1266621411 0.00001
NM_001037.5(SCN1B):c.387C>T (p.Phe129=) rs891588693 0.00001
NM_001037.5(SCN1B):c.396C>T (p.Tyr132=) rs181115510 0.00001
NM_001037.5(SCN1B):c.40+7G>T rs1600361053 0.00001
NM_001037.5(SCN1B):c.41-14T>C rs778258172 0.00001
NM_001037.5(SCN1B):c.41-8C>T rs2064220267 0.00001
NM_001037.5(SCN1B):c.448+125G>T rs2064231271 0.00001
NM_001037.5(SCN1B):c.448+137G>A rs1220622612 0.00001
NM_001037.5(SCN1B):c.448+161C>A rs1477139588 0.00001
NM_001037.5(SCN1B):c.448+163A>G rs761312032 0.00001
NM_001037.5(SCN1B):c.448+215C>G rs1015574605 0.00001
NM_001037.5(SCN1B):c.448+230C>T rs769132369 0.00001
NM_001037.5(SCN1B):c.448+77C>T rs2064230789 0.00001
NM_001037.5(SCN1B):c.448+92C>A rs750396627 0.00001
NM_001037.5(SCN1B):c.54C>T (p.Cys18=) rs1005312276 0.00001
NM_001037.5(SCN1B):c.594G>A (p.Ser198=) rs112564234 0.00001
NM_001037.5(SCN1B):c.105C>T (p.Thr35=)
NM_001037.5(SCN1B):c.123C>T (p.Ile41=)
NM_001037.5(SCN1B):c.147C>A (p.Thr49=)
NM_001037.5(SCN1B):c.147C>T (p.Thr49=)
NM_001037.5(SCN1B):c.189C>G (p.Gly63=)
NM_001037.5(SCN1B):c.201T>C (p.Phe67=)
NM_001037.5(SCN1B):c.207+10T>C rs1057523254
NM_001037.5(SCN1B):c.207+13C>G rs373809858
NM_001037.5(SCN1B):c.207+13C>T rs373809858
NM_001037.5(SCN1B):c.207+14G>C
NM_001037.5(SCN1B):c.207+16G>A rs1159911277
NM_001037.5(SCN1B):c.207+19C>A rs201872896
NM_001037.5(SCN1B):c.207+19C>T rs201872896
NM_001037.5(SCN1B):c.207+20G>A
NM_001037.5(SCN1B):c.207+20G>C
NM_001037.5(SCN1B):c.207+9del
NM_001037.5(SCN1B):c.208-18C>G
NM_001037.5(SCN1B):c.213G>A (p.Leu71=)
NM_001037.5(SCN1B):c.238C>T (p.Leu80=)
NM_001037.5(SCN1B):c.27C>A (p.Val9=) rs2151745350
NM_001037.5(SCN1B):c.286C>A (p.Arg96=)
NM_001037.5(SCN1B):c.291C>T (p.Gly97=)
NM_001037.5(SCN1B):c.330T>C (p.Asn110=)
NM_001037.5(SCN1B):c.339C>T (p.Tyr113=)
NM_001037.5(SCN1B):c.33G>C (p.Ala11=)
NM_001037.5(SCN1B):c.399G>A (p.Glu133=)
NM_001037.5(SCN1B):c.40+11G>C
NM_001037.5(SCN1B):c.40+15G>A rs72556351
NM_001037.5(SCN1B):c.40+17C>T
NM_001037.5(SCN1B):c.40+8C>T rs1600361056
NM_001037.5(SCN1B):c.41-11T>C
NM_001037.5(SCN1B):c.41-12del rs2064220229
NM_001037.5(SCN1B):c.41-19G>A
NM_001037.5(SCN1B):c.41-4dup
NM_001037.5(SCN1B):c.41-5C>T
NM_001037.5(SCN1B):c.41-7C>T rs2151745957
NM_001037.5(SCN1B):c.411C>T (p.Ser137=) rs202053988
NM_001037.5(SCN1B):c.414C>G (p.Val138=) rs757116018
NM_001037.5(SCN1B):c.429C>T (p.His143=) rs1600364945
NM_001037.5(SCN1B):c.444C>T (p.Asp148=) rs2151746505
NM_001037.5(SCN1B):c.448+113C>G
NM_001037.5(SCN1B):c.448+131G>A rs2151746593
NM_001037.5(SCN1B):c.448+152C>T
NM_001037.5(SCN1B):c.448+158A>C
NM_001037.5(SCN1B):c.448+164G>A rs781215295
NM_001037.5(SCN1B):c.448+167C>G rs529053826
NM_001037.5(SCN1B):c.448+17C>T
NM_001037.5(SCN1B):c.448+191A>G
NM_001037.5(SCN1B):c.448+211C>G rs749830952
NM_001037.5(SCN1B):c.448+215C>A
NM_001037.5(SCN1B):c.448+221C>T
NM_001037.5(SCN1B):c.448+233G>A
NM_001037.5(SCN1B):c.448+236C>T rs779470587
NM_001037.5(SCN1B):c.448+278G>A rs1057521627
NM_001037.5(SCN1B):c.448+287G>C
NM_001037.5(SCN1B):c.448+305T>C
NM_001037.5(SCN1B):c.448+308C>T rs986180682
NM_001037.5(SCN1B):c.448+337G>A rs369032304
NM_001037.5(SCN1B):c.448+39C>A
NM_001037.5(SCN1B):c.448+41G>A
NM_001037.5(SCN1B):c.448+71A>G
NM_001037.5(SCN1B):c.448+8G>A rs200222933
NM_001037.5(SCN1B):c.448+8G>T
NM_001037.5(SCN1B):c.448+92C>G rs750396627
NM_001037.5(SCN1B):c.449-14C>T rs1355096099
NM_001037.5(SCN1B):c.449-17C>T rs1279969842
NM_001037.5(SCN1B):c.508T>C (p.Leu170=) rs748491132
NM_001037.5(SCN1B):c.522C>A (p.Leu174=) rs35478147
NM_001037.5(SCN1B):c.522C>T (p.Leu174=) rs35478147
NM_001037.5(SCN1B):c.555C>T (p.Ile185=) rs1291900478
NM_001037.5(SCN1B):c.561C>G (p.Ala187=) rs587781152
NM_001037.5(SCN1B):c.627G>A (p.Glu209=)
NM_001037.5(SCN1B):c.651C>T (p.Ala217=)
NM_001037.5(SCN1B):c.69G>A (p.Glu23=) rs762553865
NM_001037.5(SCN1B):c.72G>A (p.Val24=)
NM_001037.5(SCN1B):c.78G>A (p.Ser26=) rs774401364
NM_001037.5(SCN1B):c.90C>A (p.Ala30=) rs753994622
NM_001037.5(SCN1B):c.99G>T (p.Gly33=)

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