ClinVar Miner

List of variants in gene LOC130006235, UNC93B1 studied 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: 31
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HGVS dbSNP gnomAD frequency
NM_030930.4(UNC93B1):c.97-8G>T rs539458551 0.00220
NM_030930.4(UNC93B1):c.135G>A (p.Glu45=) rs572359733 0.00119
NM_030930.4(UNC93B1):c.193C>G (p.Leu65Val) rs376191930 0.00042
NM_030930.4(UNC93B1):c.151C>G (p.Arg51Gly) rs906974288 0.00039
NM_030930.4(UNC93B1):c.97-6T>C rs755041549 0.00025
NM_030930.4(UNC93B1):c.183C>T (p.Leu61=) rs1365228419 0.00008
NM_030930.4(UNC93B1):c.136G>A (p.Glu46Lys) rs781047243 0.00004
NM_030930.4(UNC93B1):c.148C>A (p.Arg50Ser) rs934872284 0.00004
NM_030930.4(UNC93B1):c.160C>A (p.Arg54Ser) rs979062164 0.00003
NM_030930.4(UNC93B1):c.190G>A (p.Val64Met) rs370865340 0.00002
NM_030930.4(UNC93B1):c.103G>A (p.Glu35Lys) rs1442663723 0.00001
NM_030930.4(UNC93B1):c.133G>C (p.Glu45Gln) rs1382458383 0.00001
NM_030930.4(UNC93B1):c.225C>T (p.Tyr75=) rs1358908162 0.00001
NM_030930.4(UNC93B1):c.226G>A (p.Gly76Ser) rs1266485931 0.00001
NM_030930.4(UNC93B1):c.97-12C>A rs1037340676 0.00001
NM_030930.4(UNC93B1):c.108G>A (p.Leu36=)
NM_030930.4(UNC93B1):c.125A>G (p.Asn42Ser) rs1590764715
NM_030930.4(UNC93B1):c.133GAG[4] (p.Glu49del) rs767892224
NM_030930.4(UNC93B1):c.155A>G (p.Tyr52Cys) rs1314833955
NM_030930.4(UNC93B1):c.161G>A (p.Arg54His)
NM_030930.4(UNC93B1):c.170G>T (p.Arg57Leu)
NM_030930.4(UNC93B1):c.177C>A (p.Gly59=)
NM_030930.4(UNC93B1):c.190G>C (p.Val64Leu) rs370865340
NM_030930.4(UNC93B1):c.198T>C (p.Ala66=)
NM_030930.4(UNC93B1):c.210G>A (p.Gly70=)
NM_030930.4(UNC93B1):c.214A>G (p.Met72Val)
NM_030930.4(UNC93B1):c.235C>T (p.Leu79=)
NM_030930.4(UNC93B1):c.238+17G>T
NM_030930.4(UNC93B1):c.238+4G>T rs1324720845
NM_030930.4(UNC93B1):c.97-15G>A
NM_030930.4(UNC93B1):c.97-19C>T

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