List of variants in gene JAK3 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000215.4(JAK3):c.1255-79A>G	rs370696028	0.02585
NM_000215.4(JAK3):c.2978+88G>T	rs527281163	0.01772
NM_000215.4(JAK3):c.2351-58C>G	rs73922623	0.01554
NM_000215.4(JAK3):c.1787-84C>T	rs28493430	0.01388
NM_000215.4(JAK3):c.2805+71C>T	rs73020668	0.01216
NM_000215.4(JAK3):c.2978+110C>T	rs3212778	0.01199
NM_000215.4(JAK3):c.566+73G>A	rs3212727	0.01031
NM_000215.4(JAK3):c.1441+131T>C	rs3212746	0.01027
NM_000215.4(JAK3):c.1786+14A>C	rs756976635	0.00925
NM_000215.4(JAK3):c.2164G>A (p.Val722Ile)	rs3213409	0.00743
NM_000215.4(JAK3):c.452C>G (p.Pro151Arg)	rs55778349	0.00647
NM_000215.4(JAK3):c.3208-74C>T	rs115332460	0.00548
NM_000215.4(JAK3):c.-26C>T	rs199713123	0.00411
NM_000215.4(JAK3):c.631A>C (p.Arg211=)	rs56269787	0.00207
NM_000215.4(JAK3):c.108G>C (p.Gly36=)	rs149701114	0.00201
NM_000215.4(JAK3):c.3268G>A (p.Ala1090Thr)	rs144968714	0.00150
NM_000215.4(JAK3):c.1581G>A (p.Leu527=)	rs3213408	0.00121
NM_000215.4(JAK3):c.1929G>A (p.Leu643=)	rs138645044	0.00119
NM_000215.4(JAK3):c.252G>A (p.Pro84=)	rs139738701	0.00102
NM_000215.4(JAK3):c.1551T>A (p.Pro517=)	rs143936463	0.00075
NM_000215.4(JAK3):c.2235G>A (p.Pro745=)	rs149207170	0.00026
NM_000215.4(JAK3):c.1352G>A (p.Arg451Gln)	rs145751599	0.00005
NM_000215.4(JAK3):c.2772C>T (p.Ser924=)	rs199939250	0.00004
NM_000215.4(JAK3):c.2529G>A (p.Pro843=)	rs775003661	0.00002
NM_000215.4(JAK3):c.2163C>T (p.Gly721=)	rs200715301	0.00001
NM_000215.4(JAK3):c.267C>A (p.Ser89=)	rs754716735	0.00001
NM_000215.4(JAK3):c.1269T>C (p.Pro423=)	rs1555744931
NM_000215.4(JAK3):c.1914+77G>C
NM_000215.4(JAK3):c.2478A>C (p.Ser826=)	rs1599868483
NM_000215.4(JAK3):c.2643T>C (p.Asp881=)	rs1599868171
NM_000215.4(JAK3):c.291C>T (p.Val97=)
NM_000215.4(JAK3):c.741A>C (p.Pro247=)
NM_000215.4(JAK3):c.744C>G (p.Ala248=)

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.