ClinVar Miner

List of variants in gene SCN4B reported as likely benign for congenital heart disease

Included ClinVar conditions (289):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_174934.4(SCN4B):c.*3054T>C rs3741315 0.59553
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.*924_*934dup rs1370870059 0.30565
NM_174934.4(SCN4B):c.*2120A>C rs45460396 0.24417
NM_174934.4(SCN4B):c.*2879T>C rs45584835 0.24415
NM_174934.4(SCN4B):c.*2623A>G rs868344 0.24112
NM_174934.4(SCN4B):c.174C>T (p.Cys58=) rs45539032 0.03816
NM_174934.4(SCN4B):c.*1962C>T rs7934994 0.01416
NM_174934.4(SCN4B):c.*979C>A rs541268607 0.01330
NM_174934.4(SCN4B):c.*2952G>A rs76776242 0.01280
NM_174934.4(SCN4B):c.*1071T>C rs117263855 0.01170
NM_174934.4(SCN4B):c.*2496C>T rs114345754 0.01089
NM_174934.4(SCN4B):c.*889G>A rs113579428 0.01073
NM_174934.4(SCN4B):c.*1164G>A rs1793158 0.00807
NM_174934.4(SCN4B):c.*1842G>C rs117471801 0.00566
NM_174934.4(SCN4B):c.*2785C>T rs77548426 0.00502
NM_174934.4(SCN4B):c.*988_*989insA rs5795119 0.00318
NM_174934.4(SCN4B):c.*362G>T rs72546681 0.00269
NM_174934.4(SCN4B):c.*905C>G rs565174265 0.00189
NM_174934.4(SCN4B):c.*3279G>A rs145392070 0.00156
NM_174934.3(SCN4B):c.-222T>A rs191321129 0.00084
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.*1053T>C rs191989669 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.*2918A>G rs570654511 0.00004
NM_174934.4(SCN4B):c.*471A>T rs539487703 0.00004
NM_174934.4(SCN4B):c.507C>T (p.Val169=) rs759761004 0.00004
NM_174934.4(SCN4B):c.593+10T>C rs751802844 0.00002
NM_174934.4(SCN4B):c.627C>T (p.Asp209=) rs371872353 0.00002
NM_174934.4(SCN4B):c.21A>G (p.Gly7=) rs1332884912 0.00001
NM_174934.4(SCN4B):c.234+14G>A rs1300967093 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.606C>T (p.Leu202=) rs1047192753 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.*3607_*3611del rs569520041
NM_174934.4(SCN4B):c.*524dup rs66491110
NM_174934.4(SCN4B):c.*812A>G rs1317544
NM_174934.4(SCN4B):c.*986C>G rs28675746
NM_174934.4(SCN4B):c.*987C>G rs559032799
NM_174934.4(SCN4B):c.112G>C (p.Ala38Pro) rs777894412
NM_174934.4(SCN4B):c.156C>G (p.Pro52=) rs1263610504
NM_174934.4(SCN4B):c.33G>A (p.Pro11=) rs755861941
NM_174934.4(SCN4B):c.464-14C>T
NM_174934.4(SCN4B):c.501G>A (p.Leu167=)
NM_174934.4(SCN4B):c.555A>G (p.Lys185=) rs2135501534
NM_174934.4(SCN4B):c.570C>A (p.Ile190=)
NM_174934.4(SCN4B):c.594-15T>C
NM_174934.4(SCN4B):c.594-17TC[2] rs745759292
NM_174934.4(SCN4B):c.594-7T>A
NM_174934.4(SCN4B):c.597G>A (p.Lys199=) rs372596382
NM_174934.4(SCN4B):c.61+14A>G
NM_174934.4(SCN4B):c.61+15G>C
NM_174934.4(SCN4B):c.75C>T (p.Leu25=) rs1277058252

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