ClinVar Miner

List of variants in gene SCN4B reported as likely benign for Cardiovascular phenotype

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
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.617C>T (p.Ser206Leu) rs140348243 0.00010
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser) rs149868494 0.00009
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.482C>G (p.Thr161Arg) rs750329453 0.00003
NM_174934.4(SCN4B):c.618G>A (p.Ser206=) rs773921790 0.00002
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.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.78C>T (p.Pro26=) rs1326784999 0.00001
NM_174934.4(SCN4B):c.102T>C (p.Ser34=)
NM_174934.4(SCN4B):c.183C>T (p.Phe61=)
NM_174934.4(SCN4B):c.222C>T (p.Asp74=)
NM_174934.4(SCN4B):c.24C>A (p.Gly8=)
NM_174934.4(SCN4B):c.36G>A (p.Ala12=)
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.570C>A (p.Ile190=)
NM_174934.4(SCN4B):c.600G>A (p.Glu200=)
NM_174934.4(SCN4B):c.632C>G (p.Thr211Arg) rs201454653
NM_174934.4(SCN4B):c.633G>C (p.Thr211=)
NM_174934.4(SCN4B):c.75C>G (p.Leu25=)
NM_174934.4(SCN4B):c.78C>G (p.Pro26=)

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