ClinVar Miner

List of variants in gene APLP1 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001024807.3(APLP1):c.1841G>C (p.Ser614Thr) rs143425453 0.00023
NM_001024807.3(APLP1):c.1097C>G (p.Ser366Cys) rs201351812 0.00010
NM_001024807.3(APLP1):c.1897G>C (p.Glu633Gln) rs147200750 0.00010
NM_001024807.3(APLP1):c.1036G>A (p.Asp346Asn) rs753937698 0.00005
NM_001024807.3(APLP1):c.1208C>T (p.Pro403Leu) rs953366526 0.00005
NM_001024807.3(APLP1):c.685C>T (p.Arg229Trp) rs375123845 0.00004
NM_001024807.3(APLP1):c.1016C>A (p.Ser339Tyr) rs144628787 0.00003
NM_001024807.3(APLP1):c.1340T>C (p.Phe447Ser) rs1281922690 0.00003
NM_001024807.3(APLP1):c.245G>A (p.Arg82Gln) rs201483792 0.00002
NM_001024807.3(APLP1):c.623T>C (p.Val208Ala) rs769779680 0.00002
NM_001024807.3(APLP1):c.686G>A (p.Arg229Gln) rs778700083 0.00002
NM_001024807.3(APLP1):c.1198C>A (p.Gln400Lys) rs1029454156 0.00001
NM_001024807.3(APLP1):c.1513G>A (p.Glu505Lys) rs142258705 0.00001
NM_001024807.3(APLP1):c.1637A>G (p.Gln546Arg) rs771302083 0.00001
NM_001024807.3(APLP1):c.1792G>T (p.Val598Phe) rs1309406965 0.00001
NM_001024807.3(APLP1):c.1861G>A (p.Asp621Asn) rs1054963511 0.00001
NM_001024807.3(APLP1):c.374G>A (p.Ser125Asn) rs1023376553 0.00001
NM_001024807.3(APLP1):c.416G>A (p.Arg139His) rs775672735 0.00001
NM_001024807.3(APLP1):c.41G>A (p.Arg14His) rs1407343890 0.00001
NM_001024807.3(APLP1):c.709G>A (p.Val237Ile) rs1974158791 0.00001
NM_001024807.3(APLP1):c.1172C>T (p.Ala391Val)
NM_001024807.3(APLP1):c.1240C>T (p.Arg414Trp)
NM_001024807.3(APLP1):c.1253G>A (p.Arg418His)
NM_001024807.3(APLP1):c.1285C>T (p.Arg429Cys)
NM_001024807.3(APLP1):c.1432C>T (p.Arg478Trp)
NM_001024807.3(APLP1):c.1433G>A (p.Arg478Gln) rs200760118
NM_001024807.3(APLP1):c.1543T>A (p.Ser515Thr)
NM_001024807.3(APLP1):c.1585A>G (p.Thr529Ala)
NM_001024807.3(APLP1):c.1691C>T (p.Ser564Leu)
NM_001024807.3(APLP1):c.1698T>G (p.Ile566Met)
NM_001024807.3(APLP1):c.170C>T (p.Ala57Val)
NM_001024807.3(APLP1):c.1718C>A (p.Pro573Gln)
NM_001024807.3(APLP1):c.1718C>T (p.Pro573Leu)
NM_001024807.3(APLP1):c.1738C>G (p.Arg580Gly)
NM_001024807.3(APLP1):c.1820A>G (p.Lys607Arg) rs144655560
NM_001024807.3(APLP1):c.1847G>A (p.Gly616Asp) rs2513899679
NM_001024807.3(APLP1):c.190A>G (p.Thr64Ala) rs2513872215
NM_001024807.3(APLP1):c.202G>A (p.Asp68Asn) rs1307330477
NM_001024807.3(APLP1):c.332C>G (p.Thr111Arg) rs757097521
NM_001024807.3(APLP1):c.370C>T (p.Arg124Trp)
NM_001024807.3(APLP1):c.391C>A (p.Pro131Thr) rs960256475
NM_001024807.3(APLP1):c.446C>A (p.Ala149Asp)
NM_001024807.3(APLP1):c.481C>G (p.Gln161Glu)
NM_001024807.3(APLP1):c.694C>T (p.Pro232Ser) rs369442773
NM_001024807.3(APLP1):c.698C>G (p.Pro233Arg) rs367773519
NM_001024807.3(APLP1):c.757G>T (p.Val253Leu) rs1431429331
NM_001024807.3(APLP1):c.787G>A (p.Ala263Thr) rs2513880992
NM_001024807.3(APLP1):c.808G>A (p.Val270Ile) rs892180063
NM_001024807.3(APLP1):c.908A>G (p.Glu303Gly) rs2513883007
NM_001024807.3(APLP1):c.959G>A (p.Arg320His)
NM_001024807.3(APLP1):c.988C>A (p.Arg330Ser) rs1475297217

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.