ClinVar Miner

List of variants in gene FTCD reported as uncertain significance for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_006657.3(FTCD):c.*113C>T rs886057173
NM_006657.3(FTCD):c.*114A>G rs886057172
NM_006657.3(FTCD):c.*55A>G rs752959852
NM_206965.2(FTCD):c.*1C>T rs144773622
NM_206965.2(FTCD):c.-42T>C rs372968557
NM_206965.2(FTCD):c.100G>A (p.Val34Met) rs750617099
NM_206965.2(FTCD):c.1015T>A (p.Ser339Thr) rs1195012799
NM_206965.2(FTCD):c.1122G>A (p.Val374=) rs376986639
NM_206965.2(FTCD):c.1166C>G (p.Thr389Arg) rs545214029
NM_206965.2(FTCD):c.1202C>T (p.Ala401Val) rs886057174
NM_206965.2(FTCD):c.1220C>A (p.Thr407Lys) rs148920158
NM_206965.2(FTCD):c.1261-13C>G rs372484759
NM_206965.2(FTCD):c.1271G>A (p.Arg424Lys) rs779369991
NM_206965.2(FTCD):c.1291del (p.Glu431fs) rs775788856
NM_206965.2(FTCD):c.1312G>A (p.Ala438Thr)
NM_206965.2(FTCD):c.1337G>A (p.Arg446Gln) rs79021510
NM_206965.2(FTCD):c.1352C>T (p.Pro451Leu) rs376845160
NM_206965.2(FTCD):c.1358C>T (p.Thr453Met) rs200283734
NM_206965.2(FTCD):c.1364C>T (p.Ala455Val)
NM_206965.2(FTCD):c.1408C>T (p.Arg470Trp) rs199807194
NM_206965.2(FTCD):c.1409G>A (p.Arg470Gln) rs61735839
NM_206965.2(FTCD):c.153C>T (p.Phe51=) rs779166982
NM_206965.2(FTCD):c.1589C>T (p.Ala530Val) rs759031386
NM_206965.2(FTCD):c.192C>T (p.Asn64=) rs148787454
NM_206965.2(FTCD):c.197C>T (p.Ala66Val) rs199867833
NM_206965.2(FTCD):c.250C>T (p.Arg84Cys) rs576603499
NM_206965.2(FTCD):c.267C>T (p.Asp89=) rs370444672
NM_206965.2(FTCD):c.285C>T (p.Pro95=) rs572661766
NM_206965.2(FTCD):c.319T>C (p.Cys107Arg)
NM_206965.2(FTCD):c.35C>T (p.Ser12Leu) rs201753824
NM_206965.2(FTCD):c.367+13C>T rs886057175
NM_206965.2(FTCD):c.368-15C>T rs368792878
NM_206965.2(FTCD):c.36G>A (p.Ser12=) rs150970653
NM_206965.2(FTCD):c.378C>T (p.Tyr126=) rs374724805
NM_206965.2(FTCD):c.382G>A (p.Glu128Lys) rs61729373
NM_206965.2(FTCD):c.425G>A (p.Arg142Gln) rs375990689
NM_206965.2(FTCD):c.430G>A (p.Gly144Arg) rs138139105
NM_206965.2(FTCD):c.439G>A (p.Glu147Lys) rs754659947
NM_206965.2(FTCD):c.469G>A (p.Asp157Asn)
NM_206965.2(FTCD):c.476C>T (p.Ala159Val) rs200652518
NM_206965.2(FTCD):c.48C>G (p.Asn16Lys) rs369544006
NM_206965.2(FTCD):c.49C>A (p.Gln17Lys) rs776696117
NM_206965.2(FTCD):c.571G>A (p.Gly191Ser) rs376603123
NM_206965.2(FTCD):c.600G>A (p.Ala200=) rs147306849
NM_206965.2(FTCD):c.622C>T (p.Arg208Cys) rs764331074
NM_206965.2(FTCD):c.625G>A (p.Gly209Arg) rs367906516
NM_206965.2(FTCD):c.636+9G>A rs370596374
NM_206965.2(FTCD):c.643C>T (p.Arg215Cys) rs149667449
NM_206965.2(FTCD):c.750C>T (p.Tyr250=) rs112148465
NM_206965.2(FTCD):c.763C>T (p.Arg255Ter) rs140217223
NM_206965.2(FTCD):c.764_765GA[1] (p.Glu256fs) rs1568979227
NM_206965.2(FTCD):c.857G>A (p.Cys286Tyr)
NM_206965.2(FTCD):c.92C>T (p.Pro31Leu) rs371619712
NM_206965.2(FTCD):c.959G>A (p.Arg320Gln)
NM_206965.2(FTCD):c.988G>A (p.Gly330Arg) rs774835292
NM_206965.2(FTCD):c.997del (p.Arg333fs) rs1568974130

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.