List of variants in gene IFNGR1 reported by OMIM

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000416.3(IFNGR1):c.-56T>C	rs2234711	0.42896
NM_000416.3(IFNGR1):c.2T>A (p.Met1Lys)	rs387906593	0.00002
NM_000416.3(IFNGR1):c.260T>C (p.Ile87Thr)	rs104893973	0.00001
NM_000416.3(IFNGR1):c.104_107dup (p.Ile37fs)	rs587776854
NM_000416.3(IFNGR1):c.131del (p.Pro44fs)	rs587776853
NM_000416.3(IFNGR1):c.182T>A (p.Val61Glu)	rs121912715
NM_000416.3(IFNGR1):c.200+1G>A	rs587776855
NM_000416.3(IFNGR1):c.230G>A (p.Cys77Tyr)	rs104893974
NM_000416.3(IFNGR1):c.295_306del (p.Trp99_Val102del)	rs587776857
NM_000416.3(IFNGR1):c.446C>A (p.Ser149Ter)	rs387906572
NM_000416.3(IFNGR1):c.653_655del (p.Glu218del)	rs587776858
NM_000416.3(IFNGR1):c.794del (p.Phe265fs)	rs587776860
NM_000416.3(IFNGR1):c.819_822del (p.Asn274fs)	rs587776856
NM_000416.3(IFNGR1):c.819del (p.Asn274fs)	rs587776859

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.