ClinVar Miner

List of variants in gene SCN4B studied for Cardiovascular phenotype

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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_174934.4(SCN4B):c.174C>T (p.Cys58=) rs45539032 0.03816
NM_174934.4(SCN4B):c.639C>T (p.Asn213=) rs72544155 0.00341
NM_174934.4(SCN4B):c.480C>T (p.Asn160=) rs72546675 0.00083
NM_174934.4(SCN4B):c.542T>C (p.Leu181Pro) rs61065977 0.00047
NM_174934.4(SCN4B):c.607G>A (p.Val203Met) rs150312046 0.00031
NM_174934.4(SCN4B):c.194A>T (p.His65Leu) rs112363898 0.00025
NM_174934.4(SCN4B):c.18C>A (p.Asp6Glu) rs149979176 0.00021
NM_174934.4(SCN4B):c.520A>G (p.Ile174Val) rs377730779 0.00019
NM_174934.4(SCN4B):c.617C>T (p.Ser206Leu) rs140348243 0.00010
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser) rs149868494 0.00009
NM_174934.4(SCN4B):c.469G>C (p.Glu157Gln) rs746647997 0.00006
NM_174934.4(SCN4B):c.640G>A (p.Gly214Ser) rs367988277 0.00006
NM_174934.4(SCN4B):c.633G>A (p.Thr211=) rs111905160 0.00005
NM_174934.4(SCN4B):c.199C>T (p.Arg67Trp) rs775614261 0.00003
NM_174934.4(SCN4B):c.482C>G (p.Thr161Arg) rs750329453 0.00003
NM_174934.4(SCN4B):c.34G>A (p.Ala12Thr) rs752598271 0.00002
NM_174934.4(SCN4B):c.533T>C (p.Ile178Thr) rs746641404 0.00002
NM_174934.4(SCN4B):c.594-2A>G rs375535030 0.00002
NM_174934.4(SCN4B):c.618G>A (p.Ser206=) rs773921790 0.00002
NM_174934.4(SCN4B):c.115A>G (p.Thr39Ala) rs756210130 0.00001
NM_174934.4(SCN4B):c.21A>G (p.Gly7=) rs1332884912 0.00001
NM_174934.4(SCN4B):c.33G>C (p.Pro11=) rs755861941 0.00001
NM_174934.4(SCN4B):c.40T>G (p.Trp14Gly) rs946169910 0.00001
NM_174934.4(SCN4B):c.513C>T (p.Gly171=) rs368141412 0.00001
NM_174934.4(SCN4B):c.546G>A (p.Leu182=) rs1306208725 0.00001
NM_174934.4(SCN4B):c.579G>A (p.Lys193=) rs202087057 0.00001
NM_174934.4(SCN4B):c.624T>C (p.Asn208=) rs770446500 0.00001
NM_174934.4(SCN4B):c.630C>T (p.Asn210=) rs1418864816 0.00001
NM_174934.4(SCN4B):c.649G>T (p.Gly217Cys) rs371609756 0.00001
NM_174934.4(SCN4B):c.78C>T (p.Pro26=) rs1326784999 0.00001
NM_174934.4(SCN4B):c.102T>C (p.Ser34=)
NM_174934.4(SCN4B):c.104T>C (p.Val35Ala)
NM_174934.4(SCN4B):c.112G>C (p.Ala38Pro) rs777894412
NM_174934.4(SCN4B):c.183C>G (p.Phe61Leu)
NM_174934.4(SCN4B):c.183C>T (p.Phe61=)
NM_174934.4(SCN4B):c.200G>A (p.Arg67Gln)
NM_174934.4(SCN4B):c.222C>T (p.Asp74=)
NM_174934.4(SCN4B):c.223G>A (p.Ala75Thr)
NM_174934.4(SCN4B):c.231G>C (p.Lys77Asn)
NM_174934.4(SCN4B):c.234+1G>A rs1341627207
NM_174934.4(SCN4B):c.234+1G>C
NM_174934.4(SCN4B):c.234+1G>T
NM_174934.4(SCN4B):c.23_24delinsAA (p.Gly8Glu)
NM_174934.4(SCN4B):c.24C>A (p.Gly8=)
NM_174934.4(SCN4B):c.2T>G (p.Met1Arg) rs764844756
NM_174934.4(SCN4B):c.36G>A (p.Ala12=)
NM_174934.4(SCN4B):c.491T>A (p.Leu164His)
NM_174934.4(SCN4B):c.491_492delinsAG (p.Leu164Gln)
NM_174934.4(SCN4B):c.492C>G (p.Leu164=)
NM_174934.4(SCN4B):c.492C>T (p.Leu164=)
NM_174934.4(SCN4B):c.501G>A (p.Leu167=)
NM_174934.4(SCN4B):c.505G>A (p.Val169Ile)
NM_174934.4(SCN4B):c.508G>A (p.Val170Met)
NM_174934.4(SCN4B):c.538A>C (p.Ile180Leu)
NM_174934.4(SCN4B):c.556C>G (p.Leu186Val)
NM_174934.4(SCN4B):c.55_56delinsGA (p.Leu19Asp)
NM_174934.4(SCN4B):c.570C>A (p.Ile190=)
NM_174934.4(SCN4B):c.583C>T (p.Arg195Trp) rs945490950
NM_174934.4(SCN4B):c.589A>T (p.Lys197Ter)
NM_174934.4(SCN4B):c.600G>A (p.Glu200=)
NM_174934.4(SCN4B):c.610A>G (p.Ser204Gly)
NM_174934.4(SCN4B):c.632C>G (p.Thr211Arg) rs201454653
NM_174934.4(SCN4B):c.633G>C (p.Thr211=)
NM_174934.4(SCN4B):c.636_637dup (p.Asn213fs)
NM_174934.4(SCN4B):c.641G>T (p.Gly214Val)
NM_174934.4(SCN4B):c.673C>G (p.Pro225Ala)
NM_174934.4(SCN4B):c.686G>C (p.Ter229Ser)
NM_174934.4(SCN4B):c.75C>G (p.Leu25=)
NM_174934.4(SCN4B):c.78C>G (p.Pro26=)
NM_174934.4(SCN4B):c.7G>A (p.Gly3Arg)
NM_174934.4(SCN4B):c.90G>T (p.Ser30=)

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