List of variants in gene CYBB, LOC130068093 studied for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_000397.4(CYBB):c.30C>T (p.Leu10=)	rs781966553	0.00001
NM_000397.4(CYBB):c.43A>G (p.Ile15Val)	rs781809179	0.00001
NM_000397.4(CYBB):c.45+18A>G	rs781908342	0.00001
NC_000023.11:g.(?_37780009)_(37783620_?)del
NM_000397.4(CYBB):c.27G>A (p.Gly9=)
NM_000397.4(CYBB):c.27G>T (p.Gly9=)	rs979166608
NM_000397.4(CYBB):c.30C>A (p.Leu10=)	rs781966553
NM_000397.4(CYBB):c.32C>T (p.Ser11Phe)
NM_000397.4(CYBB):c.33C>T (p.Ser11=)
NM_000397.4(CYBB):c.37_45+2del	rs1556464116
NM_000397.4(CYBB):c.39T>C (p.Phe13=)
NM_000397.4(CYBB):c.40del (p.Val14fs)
NM_000397.4(CYBB):c.42C>A (p.Val14=)	rs1928916724
NM_000397.4(CYBB):c.43A>T (p.Ile15Phe)	rs781809179
NM_000397.4(CYBB):c.45+1G>T
NM_000397.4(CYBB):c.45+20A>G
NM_000397.4(CYBB):c.45+2del	rs1602173465
NM_000397.4(CYBB):c.45+2dup
NM_000397.4(CYBB):c.45+3A>C	rs1602173466
NM_000397.4(CYBB):c.45+6T>C	rs1569478551
NM_000397.4(CYBB):c.45+8C>T
NM_000397.4(CYBB):c.45+9C>G	rs2146802012

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