ClinVar Miner

List of variants in gene UNC93B1 reported as benign for central nervous system infectious disorder

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_030930.4(UNC93B1):c.1557C>G (p.Arg519=) rs7149 0.34645
NM_030930.4(UNC93B1):c.1206G>C (p.Pro402=) rs112284414 0.02461
NM_030930.4(UNC93B1):c.1163C>T (p.Ala388Val) rs11543208 0.01149
NM_030930.4(UNC93B1):c.1155C>T (p.Gly385=) rs200930438 0.00844
NM_030930.4(UNC93B1):c.1725C>G (p.Pro575=) rs568350079 0.00509
NM_030930.4(UNC93B1):c.907-5C>T rs144979304 0.00332
NM_030930.4(UNC93B1):c.1772G>A (p.Gly591Glu) rs531159136 0.00330
NM_030930.4(UNC93B1):c.393-10C>T rs117183629 0.00314
NM_030930.4(UNC93B1):c.626C>T (p.Pro209Leu) rs144399212 0.00265
NM_030930.4(UNC93B1):c.385C>A (p.Leu129Ile) rs146593182 0.00262
NM_030930.4(UNC93B1):c.1453G>A (p.Val485Met) rs199824078 0.00237
NM_030930.4(UNC93B1):c.239-6C>T rs182093266 0.00183
NM_030930.4(UNC93B1):c.96+10G>A rs188940236 0.00090
NM_030930.4(UNC93B1):c.1713T>C (p.Pro571=) rs565846179 0.00025
NM_030930.4(UNC93B1):c.1449C>T (p.Phe483=) rs371738908 0.00019
NM_030930.4(UNC93B1):c.1183C>T (p.Leu395=) rs776764518 0.00016
NM_030930.4(UNC93B1):c.1090-10dup rs760132599
NM_030930.4(UNC93B1):c.1221C>T (p.Ala407=) rs12660
NM_030930.4(UNC93B1):c.1495G>A (p.Val499Met) rs4014596
NM_030930.4(UNC93B1):c.1724_1725delinsAG (p.Pro575Gln) rs1554984685
NM_030930.4(UNC93B1):c.1768G>T (p.Gly590Trp) rs2375182
NM_030930.4(UNC93B1):c.888dup (p.Phe297fs) rs5792426

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