ClinVar Miner

List of variants in gene GTF3C4 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012204.4(GTF3C4):c.935C>T (p.Ser312Phe) rs150601105 0.00044
NM_012204.4(GTF3C4):c.328C>T (p.Pro110Ser) rs144693888 0.00030
NM_012204.4(GTF3C4):c.1805A>C (p.Glu602Ala) rs1294771949 0.00003
NM_012204.4(GTF3C4):c.1811C>T (p.Ser604Leu) rs370378462 0.00003
NM_012204.4(GTF3C4):c.2297A>G (p.Asn766Ser) rs763842441 0.00003
NM_012204.4(GTF3C4):c.2294C>G (p.Ser765Cys) rs776781321 0.00002
NM_012204.4(GTF3C4):c.143G>A (p.Arg48His) rs765083568 0.00001
NM_012204.4(GTF3C4):c.1586C>T (p.Ser529Leu) rs1024343600 0.00001
NM_012204.4(GTF3C4):c.340A>G (p.Asn114Asp) rs749149752 0.00001
NM_012204.4(GTF3C4):c.457C>T (p.Pro153Ser) rs965874077 0.00001
NM_012204.4(GTF3C4):c.8C>T (p.Thr3Met) rs1311171799 0.00001
NM_012204.4(GTF3C4):c.971A>G (p.Asn324Ser) rs1835897031 0.00001
NM_012204.4(GTF3C4):c.1046C>T (p.Ala349Val)
NM_012204.4(GTF3C4):c.127C>T (p.Pro43Ser)
NM_012204.4(GTF3C4):c.1456G>A (p.Gly486Ser) rs755530765
NM_012204.4(GTF3C4):c.1480A>G (p.Thr494Ala)
NM_012204.4(GTF3C4):c.1498G>A (p.Gly500Ser) rs1387221677
NM_012204.4(GTF3C4):c.155C>G (p.Thr52Ser) rs751151981
NM_012204.4(GTF3C4):c.157C>T (p.Arg53Trp)
NM_012204.4(GTF3C4):c.1794A>C (p.Lys598Asn)
NM_012204.4(GTF3C4):c.182A>G (p.Gln61Arg) rs1835717192
NM_012204.4(GTF3C4):c.1872A>C (p.Glu624Asp)
NM_012204.4(GTF3C4):c.1880C>A (p.Ser627Tyr) rs2539967294
NM_012204.4(GTF3C4):c.1910A>T (p.Gln637Leu)
NM_012204.4(GTF3C4):c.1963A>C (p.Thr655Pro)
NM_012204.4(GTF3C4):c.196G>A (p.Gly66Ser) rs778934641
NM_012204.4(GTF3C4):c.2276G>A (p.Arg759His) rs1393540102
NM_012204.4(GTF3C4):c.302A>G (p.Asp101Gly)
NM_012204.4(GTF3C4):c.319A>T (p.Thr107Ser)
NM_012204.4(GTF3C4):c.32C>T (p.Pro11Leu)
NM_012204.4(GTF3C4):c.40G>A (p.Asp14Asn) rs757913856
NM_012204.4(GTF3C4):c.47C>T (p.Pro16Leu) rs756998341
NM_012204.4(GTF3C4):c.481A>G (p.Met161Val)
NM_012204.4(GTF3C4):c.500C>G (p.Thr167Ser)
NM_012204.4(GTF3C4):c.565A>G (p.Asn189Asp)
NM_012204.4(GTF3C4):c.599T>C (p.Leu200Pro)
NM_012204.4(GTF3C4):c.6C>A (p.Asn2Lys) rs1022128165
NM_012204.4(GTF3C4):c.859G>A (p.Val287Met)
NM_012204.4(GTF3C4):c.878C>T (p.Pro293Leu) rs2539966176
NM_012204.4(GTF3C4):c.941G>A (p.Ser314Asn)
NM_012204.4(GTF3C4):c.974A>G (p.Asn325Ser)
NM_012204.4(GTF3C4):c.976C>G (p.Arg326Gly)

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.