ClinVar Miner

List of variants in gene REST studied for mixed neoplasm

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_005612.5(REST):c.898+15C>T rs148949163 0.00026
NM_005612.5(REST):c.2065C>T (p.Pro689Ser) rs149486440 0.00014
NM_005612.5(REST):c.2989A>G (p.Met997Val) rs373733071 0.00011
NM_005612.5(REST):c.302G>A (p.Gly101Asp) rs150412877 0.00011
NM_005612.5(REST):c.527A>G (p.His176Arg) rs375735172 0.00006
NM_005612.5(REST):c.1344A>G (p.Ile448Met) rs778247936 0.00004
NM_005612.5(REST):c.843C>T (p.Cys281=) rs751201019 0.00003
NM_005612.5(REST):c.1747A>G (p.Thr583Ala) rs752454165 0.00002
NM_005612.5(REST):c.1902G>A (p.Met634Ile) rs777213931 0.00002
NM_005612.5(REST):c.2917A>G (p.Met973Val) rs773073831 0.00002
NM_005612.5(REST):c.416A>G (p.Asp139Gly) rs112115500 0.00002
NM_005612.5(REST):c.1639G>T (p.Val547Leu) rs754696564 0.00001
NM_005612.5(REST):c.2068C>T (p.Pro690Ser) rs1169375776 0.00001
NM_005612.5(REST):c.2780A>G (p.Asn927Ser) rs557500462 0.00001
NM_005612.5(REST):c.831_832del (p.Cys278fs) rs869025310 0.00001
NM_005612.5(REST):c.965A>G (p.His322Arg) rs869025312 0.00001
NM_005612.5(REST):c.1255A>G (p.Thr419Ala)
NM_005612.5(REST):c.1298G>A (p.Arg433Gln)
NM_005612.5(REST):c.1309T>A (p.Leu437Met)
NM_005612.5(REST):c.1313C>A (p.Pro438His)
NM_005612.5(REST):c.1367A>G (p.Asp456Gly)
NM_005612.5(REST):c.1435C>T (p.Pro479Ser)
NM_005612.5(REST):c.1436C>T (p.Pro479Leu)
NM_005612.5(REST):c.1583A>G (p.His528Arg)
NM_005612.5(REST):c.1690A>C (p.Lys564Gln)
NM_005612.5(REST):c.1701G>C (p.Glu567Asp)
NM_005612.5(REST):c.1881G>T (p.Gln627His) rs1720922537
NM_005612.5(REST):c.1882G>A (p.Val628Met)
NM_005612.5(REST):c.1919A>T (p.Glu640Val)
NM_005612.5(REST):c.2032G>T (p.Ala678Ser) rs367688230
NM_005612.5(REST):c.2050C>G (p.His684Asp) rs1720935811
NM_005612.5(REST):c.2053A>G (p.Met685Val)
NM_005612.5(REST):c.2063C>G (p.Pro688Arg)
NM_005612.5(REST):c.2076_2120del (p.Thr693_Glu707del)
NM_005612.5(REST):c.2093T>C (p.Val698Ala)
NM_005612.5(REST):c.2259_2306del (p.Met753_Pro768del) rs369803397
NM_005612.5(REST):c.2307A>G (p.Ile769Met) rs766485057
NM_005612.5(REST):c.2314G>A (p.Val772Ile)
NM_005612.5(REST):c.2741A>G (p.Asn914Ser)
NM_005612.5(REST):c.2743G>C (p.Glu915Gln)
NM_005612.5(REST):c.2753A>G (p.His918Arg)
NM_005612.5(REST):c.2936_2938del (p.Val979del)
NM_005612.5(REST):c.2945G>A (p.Arg982His)
NM_005612.5(REST):c.2992G>A (p.Ala998Thr) rs1720989281
NM_005612.5(REST):c.3098A>G (p.His1033Arg) rs572949989
NM_005612.5(REST):c.3107G>T (p.Arg1036Leu)
NM_005612.5(REST):c.3140C>G (p.Ala1047Gly)
NM_005612.5(REST):c.3239A>G (p.Asn1080Ser)
NM_005612.5(REST):c.412A>G (p.Lys138Glu)
NM_005612.5(REST):c.439G>A (p.Ala147Thr)
NM_005612.5(REST):c.458G>A (p.Ser153Asn)
NM_005612.5(REST):c.461C>T (p.Ser154Leu)
NM_005612.5(REST):c.608C>G (p.Ser203Cys)
NM_005612.5(REST):c.657C>G (p.Asp219Glu)
NM_005612.5(REST):c.737G>A (p.Arg246Gln)
NM_005612.5(REST):c.773_776del (p.Val258fs) rs869025311

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