List of variants in gene combination AIP, LOC130006206 reported as not provided 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003977.4(AIP):c.145G>A (p.Val49Met)	rs1063385	0.00006
NM_003977.4(AIP):c.135C>T (p.Asp45=)	rs181969066	0.00004
NM_003977.4(AIP):c.174G>C (p.Lys58Asn)	rs267606539	0.00001
NM_003977.4(AIP):c.140_163del (p.Gly47_Arg54del)	rs267606537
NM_003977.4(AIP):c.166C>A (p.Arg56Ser)	rs267606538
NM_003977.4(AIP):c.241C>T (p.Arg81Ter)	rs267606541
NM_003977.4(AIP):c.245_249del (p.Glu82fs)	rs267606542
NM_003977.4(AIP):c.249G>T (p.Gly83=)	rs104895072
NM_003977.4(AIP):c.250G>A (p.Glu84Lys)	rs267606543

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