ClinVar Miner

List of variants in gene SUFU reported as likely pathogenic for central nervous system neoplasm

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NC_000010.10:g.(?_104352329)_(104377195_?)dup
NM_016169.4(SUFU):c.1023-2A>T rs1060501105
NM_016169.4(SUFU):c.1157+1G>A
NM_016169.4(SUFU):c.1365+1G>A rs2063794106
NM_016169.4(SUFU):c.1391G>A (p.Trp464Ter) rs2135959437
NM_016169.4(SUFU):c.182+1G>A rs2135598885
NM_016169.4(SUFU):c.182+3A>C rs1589970228
NM_016169.4(SUFU):c.183-1G>A rs1554841447
NM_016169.4(SUFU):c.183-1G>T
NM_016169.4(SUFU):c.183-2A>C rs2135619894
NM_016169.4(SUFU):c.183-4_247del
NM_016169.4(SUFU):c.317+1G>A rs2135621012
NM_016169.4(SUFU):c.318-1G>C rs2135742927
NM_016169.4(SUFU):c.597+1G>C rs1590062006
NM_016169.4(SUFU):c.683+1G>A rs2135870923
NM_016169.4(SUFU):c.684-2A>G rs1590063305
NM_016169.4(SUFU):c.911-1G>T
NM_016169.4(SUFU):c.911-2A>C

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