ClinVar Miner

List of variants in gene ALG9 reported as uncertain significance for congenital disorder of glycosylation type I

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 112
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024740.2(ALG9):c.*2473A>T rs2554994 0.69652
NM_024740.2(ALG9):c.*2474A>T rs376483443 0.04275
NM_024740.2(ALG9):c.*1607C>T rs117488631 0.00826
NM_024740.2(ALG9):c.*1680G>T rs563719515 0.00575
NM_024740.2(ALG9):c.*1624A>C rs117091304 0.00485
NM_024740.2(ALG9):c.*2230A>C rs116530919 0.00264
NM_024740.2(ALG9):c.*3471A>G rs186742619 0.00264
NM_024740.2(ALG9):c.*1722C>T rs186477879 0.00192
NM_024740.2(ALG9):c.*3423T>C rs78243190 0.00176
NM_024740.2(ALG9):c.1603-509A>G rs115136012 0.00163
NM_024740.2(ALG9):c.*3519C>A rs569799426 0.00145
NM_024740.2(ALG9):c.*1420C>G rs143933458 0.00121
NM_024740.2(ALG9):c.*3757T>C rs530143933 0.00093
NM_024740.2(ALG9):c.*3175G>A rs146182772 0.00078
NM_024740.2(ALG9):c.*314G>A rs781928817 0.00077
NM_024740.2(ALG9):c.*823A>G rs528387467 0.00058
NM_024740.2(ALG9):c.*1977A>G rs181231005 0.00043
NM_024740.2(ALG9):c.*2114C>T rs45452093 0.00034
NM_024740.2(ALG9):c.*2287A>G rs185264895 0.00034
NM_024740.2(ALG9):c.*2414T>G rs189536081 0.00034
NM_024740.2(ALG9):c.*1536T>C rs782678326 0.00032
NM_024740.2(ALG9):c.694G>C (p.Ala232Pro) rs36111204 0.00032
NM_024740.2(ALG9):c.741G>T (p.Arg247Ser) rs200946042 0.00026
NM_024740.2(ALG9):c.1489A>G (p.Ile497Val) rs138584071 0.00025
NM_024740.2(ALG9):c.*2472T>A rs886047667 0.00023
NM_024740.2(ALG9):c.*2457G>T rs201995459 0.00022
NM_024740.2(ALG9):c.*3213G>A rs939244636 0.00021
NM_024740.2(ALG9):c.*1832A>C rs772136205 0.00017
NM_024740.2(ALG9):c.*906C>A rs147670080 0.00010
NM_024740.2(ALG9):c.-58A>G rs782440068 0.00010
NM_024740.2(ALG9):c.*2233A>G rs886047674 0.00009
NM_024740.2(ALG9):c.*229A>G rs781789551 0.00009
NM_024740.2(ALG9):c.*2907A>T rs782731018 0.00008
NM_024740.2(ALG9):c.*305C>T rs782183793 0.00006
NM_024740.2(ALG9):c.*523T>C rs536072357 0.00006
NM_024740.2(ALG9):c.*4141G>C rs541035545 0.00004
NM_024740.2(ALG9):c.*763T>C rs886047680 0.00004
NM_024740.2(ALG9):c.*1687A>T rs367569393 0.00003
NM_024740.2(ALG9):c.*2339T>G rs886047673 0.00003
NM_024740.2(ALG9):c.*306G>A rs886047683 0.00003
NM_024740.2(ALG9):c.*773A>G rs886047679 0.00003
NM_024740.2(ALG9):c.1660C>T (p.Arg554Trp) rs782084496 0.00003
NM_024740.2(ALG9):c.*1311A>G rs912924184 0.00002
NM_024740.2(ALG9):c.188A>G (p.Lys63Arg) rs781991188 0.00002
NM_024740.2(ALG9):c.388A>G (p.Ile130Val) rs782298472 0.00002
NM_024740.2(ALG9):c.*2342G>A rs532591210 0.00001
NM_024740.2(ALG9):c.*3079C>T rs886047660 0.00001
NM_024740.2(ALG9):c.*3125A>T rs547384257 0.00001
NM_024740.2(ALG9):c.*3212C>T rs528920657 0.00001
NM_024740.2(ALG9):c.*365A>G rs886047682 0.00001
NM_024740.2(ALG9):c.*726C>G rs1414677485 0.00001
NM_024740.2(ALG9):c.*77G>A rs984910253 0.00001
NM_024740.2(ALG9):c.*788A>G rs559698025 0.00001
NM_024740.2(ALG9):c.1166C>T (p.Ala389Val) rs1555122792 0.00001
NM_024740.2(ALG9):c.1384A>G (p.Ile462Val) rs782350313 0.00001
NM_024740.2(ALG9):c.1502T>A (p.Phe501Tyr) rs541537158 0.00001
NM_024740.2(ALG9):c.326A>G (p.Tyr109Cys) rs782251524 0.00001
NM_024740.2(ALG9):c.535C>T (p.Leu179Phe) rs782147690 0.00001
NM_024740.2(ALG9):c.879T>G (p.His293Gln) rs1285072714 0.00001
NM_024740.2(ALG9):c.*1297A>G rs577487864
NM_024740.2(ALG9):c.*1766A>G rs886047676
NM_024740.2(ALG9):c.*243G>A rs886047684
NM_024740.2(ALG9):c.*2443T>A rs146821834
NM_024740.2(ALG9):c.*2592T>C rs886047661
NM_024740.2(ALG9):c.*2597G>C rs1591752692
NM_024740.2(ALG9):c.*2648G>A rs1946165207
NM_024740.2(ALG9):c.*3798A>G rs1946041440
NM_024740.2(ALG9):c.*532C>T rs886047681
NM_024740.2(ALG9):c.1015C>T (p.His339Tyr)
NM_024740.2(ALG9):c.1060A>T (p.Met354Leu)
NM_024740.2(ALG9):c.1077A>G (p.Ile359Met)
NM_024740.2(ALG9):c.1091A>G (p.Gln364Arg) rs1956094478
NM_024740.2(ALG9):c.1174-19T>G
NM_024740.2(ALG9):c.1177A>C (p.Ser393Arg)
NM_024740.2(ALG9):c.1197A>G (p.Lys399=)
NM_024740.2(ALG9):c.1212G>T (p.Val404=)
NM_024740.2(ALG9):c.1226G>T (p.Arg409Leu) rs929508101
NM_024740.2(ALG9):c.1317G>C (p.Leu439=)
NM_024740.2(ALG9):c.1324+6T>G
NM_024740.2(ALG9):c.1325-17A>G
NM_024740.2(ALG9):c.1352C>G (p.Pro451Arg)
NM_024740.2(ALG9):c.1364G>T (p.Arg455Leu)
NM_024740.2(ALG9):c.1382C>T (p.Thr461Ile)
NM_024740.2(ALG9):c.1399G>A (p.Glu467Lys) rs782023699
NM_024740.2(ALG9):c.1406G>A (p.Arg469Lys)
NM_024740.2(ALG9):c.1431A>G (p.Lys477=)
NM_024740.2(ALG9):c.1469A>T (p.Asp490Val)
NM_024740.2(ALG9):c.1550G>A (p.Arg517Gln)
NM_024740.2(ALG9):c.1588G>A (p.Glu530Lys) rs121908022
NM_024740.2(ALG9):c.1598G>C (p.Arg533Thr)
NM_024740.2(ALG9):c.1604T>C (p.Ile535Thr)
NM_024740.2(ALG9):c.1645A>G (p.Met549Val)
NM_024740.2(ALG9):c.1682A>G (p.Asn561Ser)
NM_024740.2(ALG9):c.1753G>A (p.Ala585Thr)
NM_024740.2(ALG9):c.1760A>G (p.Tyr587Cys)
NM_024740.2(ALG9):c.1765C>G (p.Pro589Ala)
NM_024740.2(ALG9):c.1768T>C (p.Phe590Leu)
NM_024740.2(ALG9):c.1780C>T (p.Gln594Ter) rs1555064204
NM_024740.2(ALG9):c.1820G>A (p.Arg607Gln)
NM_024740.2(ALG9):c.222C>T (p.Leu74=)
NM_024740.2(ALG9):c.279C>T (p.Tyr93=)
NM_024740.2(ALG9):c.360T>C (p.His120=)
NM_024740.2(ALG9):c.482T>C (p.Val161Ala)
NM_024740.2(ALG9):c.596C>G (p.Thr199Ser)
NM_024740.2(ALG9):c.691G>A (p.Ala231Thr)
NM_024740.2(ALG9):c.739A>G (p.Arg247Gly)
NM_024740.2(ALG9):c.793C>T (p.Pro265Ser)
NM_024740.2(ALG9):c.880G>A (p.Gly294Arg)
NM_024740.2(ALG9):c.888T>G (p.Asp296Glu)
NM_024740.2(ALG9):c.910T>C (p.Tyr304His)
NM_024740.2(ALG9):c.917A>G (p.Tyr306Cys)
NM_024740.2(ALG9):c.966C>T (p.Leu322=)

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.