ClinVar Miner

List of variants in gene GLI2 reported as uncertain significance for not specified

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001374353.1(GLI2):c.3672G>A (p.Met1224Ile) rs138191075 0.00041
NM_001374353.1(GLI2):c.4402C>G (p.Pro1468Ala) rs145958673 0.00009
NM_001374353.1(GLI2):c.2253G>A (p.Leu751=) rs140033553 0.00004
NM_001374353.1(GLI2):c.2284C>T (p.Pro762Ser) rs773216992 0.00002
NM_001374353.1(GLI2):c.3035C>T (p.Pro1012Leu) rs765093621 0.00001
GRCh37/hg19 2q14.2(chr2:121570407-121739448)x3
GRCh37/hg19 2q14.2(chr2:121728206-121799987)
GRCh37/hg19 2q14.2(chr2:121728275-121792474)
GRCh37/hg19 2q14.2(chr2:121733319-121923165)
NM_001374353.1(GLI2):c.1010C>T (p.Thr337Met)
NM_001374353.1(GLI2):c.1298C>T (p.Thr433Ile)
NM_001374353.1(GLI2):c.1394A>C (p.Lys465Thr)
NM_001374353.1(GLI2):c.1518C>A (p.His506Gln)
NM_001374353.1(GLI2):c.1639T>G (p.Tyr547Asp) rs1015526827
NM_001374353.1(GLI2):c.1672T>C (p.Tyr558His) rs763503195
NM_001374353.1(GLI2):c.1676C>T (p.Thr559Ile)
NM_001374353.1(GLI2):c.178G>C (p.Ala60Pro)
NM_001374353.1(GLI2):c.1861G>A (p.Glu621Lys)
NM_001374353.1(GLI2):c.2118G>A (p.Met706Ile)
NM_001374353.1(GLI2):c.2939C>T (p.Pro980Leu)
NM_001374353.1(GLI2):c.3190G>T (p.Gly1064Cys)
NM_001374353.1(GLI2):c.3367A>G (p.Asn1123Asp)
NM_001374353.1(GLI2):c.4027G>C (p.Gly1343Arg)
NM_001374353.1(GLI2):c.649C>G (p.Arg217Gly) rs149819397

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