List of variants in gene SLC25A11 reported as pathogenic for central nervous system neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003562.5(SLC25A11):c.107_108del (p.Thr36fs)	rs1374026152
NM_003562.5(SLC25A11):c.421G>A (p.Glu141Lys)	rs1567651815
NM_003562.5(SLC25A11):c.439A>G (p.Met147Val)	rs1203876038
NM_003562.5(SLC25A11):c.708C>T (p.Ala236=)	rs1567650874
NM_003562.5(SLC25A11):c.715C>A (p.Pro239Thr)	rs1567650859

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