ClinVar Miner

List of variants in gene SCN4B studied for not provided

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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_174934.4(SCN4B):c.593+146C>T rs668468 0.65832
NM_174934.4(SCN4B):c.*3054T>C rs3741315 0.59944
NM_174934.4(SCN4B):c.*785G>A rs1814964 0.57662
NM_174934.4(SCN4B):c.*1334G>A rs7124127 0.51745
NM_174934.4(SCN4B):c.464-259C>T rs11216781 0.38247
NM_174934.4(SCN4B):c.464-113C>T rs656445 0.35324
NM_174934.4(SCN4B):c.593+117G>A rs644287 0.35005
NM_174934.4(SCN4B):c.*2879T>C rs45584835 0.24415
NM_174934.4(SCN4B):c.*2120A>C rs45460396 0.24260
NM_174934.4(SCN4B):c.*2623A>G rs868344 0.24112
NM_174934.4(SCN4B):c.593+62C>T rs12804550 0.16572
NM_174934.4(SCN4B):c.174C>T (p.Cys58=) rs45539032 0.03816
NM_174934.4(SCN4B):c.463+270G>C rs7124973 0.03399
NM_174934.4(SCN4B):c.464-127G>A rs656469 0.03256
NM_174934.4(SCN4B):c.464-243T>C rs12269828 0.02825
NM_174934.4(SCN4B):c.464-101G>A rs114725203 0.02714
NM_174934.4(SCN4B):c.464-100G>A rs115987164 0.02713
NM_174934.4(SCN4B):c.594-80A>C rs66549461 0.02604
NM_174934.4(SCN4B):c.593+274C>T rs76447720 0.00795
NC_000011.10:g.118153182dup rs141649734 0.00711
NC_000011.10:g.118152998G>C rs72544161 0.00637
NC_000011.10:g.118152965G>A rs753866716 0.00459
NM_174934.4(SCN4B):c.61+42A>T rs200187535 0.00424
NM_174934.4(SCN4B):c.639C>T (p.Asn213=) rs72544155 0.00328
NM_174934.4(SCN4B):c.*208A>C rs574719547 0.00293
NM_174934.4(SCN4B):c.*362G>T rs72546681 0.00269
NM_174934.3(SCN4B):c.-222T>A rs191321129 0.00084
NM_174934.4(SCN4B):c.*2939G>C rs757631990 0.00077
NM_174934.4(SCN4B):c.*125C>T rs567025946 0.00066
NM_174934.4(SCN4B):c.*961A>G rs561492722 0.00058
NM_174934.4(SCN4B):c.62-260G>A rs113939995 0.00054
NM_174934.4(SCN4B):c.542T>C (p.Leu181Pro) rs61065977 0.00048
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.-29C>A rs367975000 0.00023
NM_174934.4(SCN4B):c.18C>A (p.Asp6Glu) rs149979176 0.00019
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser) rs149868494 0.00015
NM_174934.4(SCN4B):c.617C>T (p.Ser206Leu) rs140348243 0.00009
NM_174934.4(SCN4B):c.*7C>T rs79071006 0.00007
NM_174934.4(SCN4B):c.34G>A (p.Ala12Thr) rs752598271 0.00002
NM_174934.4(SCN4B):c.482C>G (p.Thr161Arg) rs750329453 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.*10C>T rs759936364 0.00001
NM_174934.4(SCN4B):c.*328G>A rs1167630754 0.00001
NM_174934.4(SCN4B):c.103G>A (p.Val35Met) rs1322792651 0.00001
NM_174934.4(SCN4B):c.208T>C (p.Tyr70His) rs1029021066 0.00001
NM_174934.4(SCN4B):c.649G>T (p.Gly217Cys) rs371609756 0.00001
NC_000011.10:g.118152851G>C rs865930367
NM_174934.3(SCN4B):c.-178C>T rs865930367
NM_174934.4(SCN4B):c.*158C>T rs1948017682
NM_174934.4(SCN4B):c.*812A>G rs1317544
NM_174934.4(SCN4B):c.*986C>G rs28675746
NM_174934.4(SCN4B):c.*987_*989dup rs5795117
NM_174934.4(SCN4B):c.-144T>G rs1440882337
NM_174934.4(SCN4B):c.-49C>T rs2135510535
NM_174934.4(SCN4B):c.-91T>G rs1354339534
NM_174934.4(SCN4B):c.112G>C (p.Ala38Pro) rs777894412
NM_174934.4(SCN4B):c.174del (p.Phe59fs) rs2135505174
NM_174934.4(SCN4B):c.196T>C (p.Phe66Leu) rs1057524836
NM_174934.4(SCN4B):c.463+205_463+206insCTCTTAGC rs45555339
NM_174934.4(SCN4B):c.464-132del rs146941709
NM_174934.4(SCN4B):c.468del (p.Glu157fs) rs2135501698
NM_174934.4(SCN4B):c.589A>G (p.Lys197Glu) rs1230446349
NM_174934.4(SCN4B):c.632C>G (p.Thr211Arg) rs201454653
NM_174934.4(SCN4B):c.632C>T (p.Thr211Met) rs201454653
NM_174934.4(SCN4B):c.644_648del (p.Leu215fs) rs778693616
NM_174934.4(SCN4B):c.647C>T (p.Pro216Leu) rs1001219641
NM_174934.4(SCN4B):c.679A>G (p.Lys227Glu) rs1555096401

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