ClinVar Miner

List of variants in gene combination LOC130067574, TNFRSF13C reported as likely benign for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_052945.4(TNFRSF13C):c.62C>G (p.Pro21Arg) rs77874543 0.05538
NM_052945.4(TNFRSF13C):c.191G>T (p.Gly64Val) rs547352394 0.00722
NM_052945.4(TNFRSF13C):c.192C>T (p.Gly64=) rs529563231 0.00721
NM_052945.4(TNFRSF13C):c.282C>T (p.Val94=) rs190252814 0.00351
NM_052945.4(TNFRSF13C):c.317G>A (p.Arg106Gln) rs150374940 0.00202
NM_052945.4(TNFRSF13C):c.102C>T (p.Ala34=) rs567541615 0.00147
NM_052945.4(TNFRSF13C):c.177G>T (p.Pro59=) rs1019575191 0.00019
NM_052945.4(TNFRSF13C):c.213G>A (p.Ala71=) rs767759337 0.00019
NM_052945.4(TNFRSF13C):c.132A>G (p.Lys44=) rs920471641 0.00006
NM_052945.4(TNFRSF13C):c.137-7del rs1299671576 0.00004
NM_052945.4(TNFRSF13C):c.307C>A (p.Arg103=) rs369626832 0.00004
NM_052945.4(TNFRSF13C):c.82C>T (p.Leu28=) rs1341767498 0.00004
NM_052945.4(TNFRSF13C):c.120G>A (p.Thr40=) rs2077634351 0.00001
NM_052945.4(TNFRSF13C):c.174G>A (p.Gln58=) rs1336911972 0.00001
NM_052945.4(TNFRSF13C):c.195G>A (p.Ala65=) rs1408228920 0.00001
NM_052945.4(TNFRSF13C):c.240C>T (p.Gly80=) rs776184560 0.00001
NM_052945.4(TNFRSF13C):c.264A>G (p.Ala88=) rs778024793 0.00001
NM_052945.4(TNFRSF13C):c.27G>C (p.Arg9=) rs1220980554 0.00001
NM_052945.4(TNFRSF13C):c.33G>A (p.Arg11=) rs1041505676 0.00001
NM_052945.4(TNFRSF13C):c.123G>A (p.Pro41=)
NM_052945.4(TNFRSF13C):c.126G>A (p.Arg42=) rs2146589962
NM_052945.4(TNFRSF13C):c.129G>T (p.Pro43=)
NM_052945.4(TNFRSF13C):c.136+17G>A rs2146589907
NM_052945.4(TNFRSF13C):c.137-15C>T
NM_052945.4(TNFRSF13C):c.137-41_137-19dup
NM_052945.4(TNFRSF13C):c.138C>G (p.Ala46=)
NM_052945.4(TNFRSF13C):c.156G>A (p.Ala52=)
NM_052945.4(TNFRSF13C):c.15C>A (p.Pro5=)
NM_052945.4(TNFRSF13C):c.204C>T (p.Gly68=)
NM_052945.4(TNFRSF13C):c.225C>G (p.Pro75=)
NM_052945.4(TNFRSF13C):c.228G>T (p.Gly76=)
NM_052945.4(TNFRSF13C):c.22C>T (p.Leu8=)
NM_052945.4(TNFRSF13C):c.231G>A (p.Leu77=)
NM_052945.4(TNFRSF13C):c.237T>C (p.Phe79=)
NM_052945.4(TNFRSF13C):c.252G>A (p.Leu84=) rs886057589
NM_052945.4(TNFRSF13C):c.255G>C (p.Leu85=) rs544076556
NM_052945.4(TNFRSF13C):c.276G>C (p.Ala92=) rs752794297
NM_052945.4(TNFRSF13C):c.288G>C (p.Val96=)
NM_052945.4(TNFRSF13C):c.36C>T (p.Asp12=)
NM_052945.4(TNFRSF13C):c.39G>A (p.Ala13=)
NM_052945.4(TNFRSF13C):c.51G>T (p.Thr17=) rs988308951
NM_052945.4(TNFRSF13C):c.81G>T (p.Leu27=)
NM_052945.4(TNFRSF13C):c.87C>T (p.Val29=)

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.