ClinVar Miner

List of variants in gene TMC6 reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001127198.5(TMC6):c.1082+5T>C rs2613522 0.39238
NM_001127198.5(TMC6):c.373T>C (p.Trp125Arg) rs2748427 0.29034
NM_001127198.5(TMC6):c.457C>T (p.Leu153Phe) rs12449858 0.09127
NM_001127198.5(TMC6):c.1083-4C>G rs2057188 0.07968
NM_001127198.5(TMC6):c.1716-6del rs3841687 0.05439
NM_001127198.5(TMC6):c.2021+11C>T rs143140501 0.02510
NM_001127198.5(TMC6):c.859G>A (p.Val287Ile) rs8078238 0.01692
NM_001127198.5(TMC6):c.1482C>T (p.Ala494=) rs61739261 0.01419
NM_001127198.5(TMC6):c.2355-4G>A rs79153946 0.01119
NM_001127198.5(TMC6):c.1228-8G>A rs150703149 0.00990
NM_001127198.5(TMC6):c.1505C>T (p.Pro502Leu) rs75400929 0.00763
NM_001127198.5(TMC6):c.1471C>T (p.Arg491Cys) rs114853749 0.00494
NM_001127198.5(TMC6):c.1276G>A (p.Gly426Arg) rs61744921 0.00430
NM_001127198.5(TMC6):c.181+6C>T rs186208897 0.00362
NM_001127198.5(TMC6):c.891+17A>G rs201082179 0.00353
NM_001127198.5(TMC6):c.838G>A (p.Ala280Thr) rs146371375 0.00335
NM_001127198.5(TMC6):c.393C>T (p.Tyr131=) rs143883680 0.00290
NM_001127198.5(TMC6):c.2022-14G>A rs188155233 0.00270
NM_001127198.5(TMC6):c.1536-4G>A rs117553598 0.00265
NM_001127198.5(TMC6):c.1592G>A (p.Arg531His) rs146998467 0.00178
NM_001127198.5(TMC6):c.858C>T (p.Pro286=) rs199827221 0.00159
NM_001127198.5(TMC6):c.2354+10C>T rs199765733 0.00121
NM_001127198.5(TMC6):c.846G>A (p.Pro282=) rs375656448 0.00061
NM_001127198.5(TMC6):c.1842C>T (p.Pro614=) rs150820026 0.00055
NM_001127198.5(TMC6):c.1536-5C>T rs201780305 0.00051
NM_001127198.5(TMC6):c.969G>A (p.Leu323=) rs139035008 0.00029
NM_001127198.5(TMC6):c.666C>T (p.Ser222=) rs371379212 0.00026
NM_001127198.5(TMC6):c.1146C>T (p.Thr382=) rs3818144 0.00020
NM_001127198.5(TMC6):c.1332C>T (p.Thr444=) rs373324506 0.00011
NM_001127198.5(TMC6):c.1888-13C>G rs758762200 0.00004
NM_001127198.5(TMC6):c.156G>A (p.Leu52=) rs201282273 0.00001
NM_001127198.5(TMC6):c.430+17T>C rs760918274 0.00001
NM_001127198.5(TMC6):c.1383+16del rs778386990
NM_001127198.5(TMC6):c.1715+9del
NM_001127198.5(TMC6):c.1950C>T (p.Thr650=) rs2613516
NM_001127198.5(TMC6):c.57-18C>T rs202180344
NM_001127198.5(TMC6):c.57-18dup rs771219760
NM_001127198.5(TMC6):c.704A>G (p.Lys235Arg) rs80354176

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