List of variants in gene combination CTSC, LOC130006572 reported as uncertain significance for immune system disorder

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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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001814.6(CTSC):c.-48G>A	rs200415443	0.00033
NM_001814.6(CTSC):c.29C>T (p.Ala10Val)	rs765499436	0.00010
NM_001814.6(CTSC):c.-49C>T	rs779871521	0.00009
NM_001814.6(CTSC):c.12G>A (p.Gly4=)	rs755959403	0.00001
NM_001814.6(CTSC):c.1A>G (p.Met1Val)	rs886048742	0.00001
NM_001814.6(CTSC):c.81T>G (p.Pro27=)	rs1370319468	0.00001
NM_001814.6(CTSC):c.-23C>G	rs886048743
NM_001814.6(CTSC):c.-55C>T
NM_001814.6(CTSC):c.-7C>A	rs770352776
NM_001814.6(CTSC):c.127G>T (p.Val43Leu)
NM_001814.6(CTSC):c.134C>T (p.Ser45Phe)
NM_001814.6(CTSC):c.140G>T (p.Gly47Val)
NM_001814.6(CTSC):c.16T>G (p.Ser6Ala)
NM_001814.6(CTSC):c.21G>C (p.Leu7Phe)
NM_001814.6(CTSC):c.21G>T (p.Leu7Phe)
NM_001814.6(CTSC):c.37C>A (p.Leu13Met)
NM_001814.6(CTSC):c.43C>T (p.Leu15Phe)
NM_001814.6(CTSC):c.4G>C (p.Gly2Arg)
NM_001814.6(CTSC):c.53G>A (p.Gly18Asp)
NM_001814.6(CTSC):c.71G>A (p.Cys24Tyr)
NM_001814.6(CTSC):c.94T>C (p.Tyr32His)
NM_001814.6(CTSC):c.95A>G (p.Tyr32Cys)

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