List of variants in gene AICDA reported by CeGaT Center for Human Genetics Tuebingen

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020661.4(AICDA):c.210A>G (p.Leu70=)	rs104894984	0.00916
NM_020661.4(AICDA):c.48A>G (p.Lys16=)	rs186739900	0.00117
NM_020661.4(AICDA):c.428-4G>T	rs77429608	0.00081
NM_020661.4(AICDA):c.441C>A (p.Cys147Ter)	rs104894323	0.00001
NM_020661.4(AICDA):c.160G>C (p.Gly54Arg)	rs1565509771
NM_020661.4(AICDA):c.203G>A (p.Trp68Ter)	rs104894325
NM_020661.4(AICDA):c.415A>G (p.Met139Val)	rs104894322
NM_020661.4(AICDA):c.428-13_428-5del
NM_020661.4(AICDA):c.428-1G>T	rs766361035
NM_020661.4(AICDA):c.568C>G (p.Arg190Gly)	rs769399833
NM_020661.4(AICDA):c.568C>T (p.Arg190Ter)	rs769399833
NM_020661.4(AICDA):c.92A>G (p.Tyr31Cys)	rs1057519097

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.