List of variants in gene CTNNA3 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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys)	rs41274090	0.01060
NM_013266.4(CTNNA3):c.33C>T (p.Ile11=)	rs61735044	0.00206
NM_013266.4(CTNNA3):c.2172A>C (p.Pro724=)	rs116662854	0.00191
NM_013266.4(CTNNA3):c.580-8C>T	rs141983252	0.00170
NM_013266.4(CTNNA3):c.1453A>T (p.Thr485Ser)	rs140913916	0.00130
NM_013266.4(CTNNA3):c.1132C>T (p.Arg378Cys)	rs187752783	0.00044
NM_013266.4(CTNNA3):c.935C>T (p.Ala312Val)	rs758173783	0.00003
NM_013266.4(CTNNA3):c.767C>T (p.Ser256Leu)	rs1864559262	0.00001
GRCh37/hg19 10q21.3(chr10:68199177-68348456)x1
NM_013266.4(CTNNA3):c.1048-7T>C
NM_013266.4(CTNNA3):c.1836G>T (p.Lys612Asn)	rs774209973
NM_013266.4(CTNNA3):c.1903G>T (p.Asp635Tyr)
NM_013266.4(CTNNA3):c.2265+2T>G
NM_013266.4(CTNNA3):c.240T>C (p.Ala80=)
NM_013266.4(CTNNA3):c.580-59152G>A
NM_013266.4(CTNNA3):c.722T>C (p.Val241Ala)
NM_013266.4(CTNNA3):c.946del (p.Asp316fs)	rs2132138021
NM_013266.4(CTNNA3):c.969dup (p.His324fs)	rs1212779512
NM_013266.4(CTNNA3):c.987C>T (p.Ile329=)

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.