ClinVar Miner

List of variants in gene MLH3 studied for endometrial disorder

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile) rs41555714 0.00048
NM_001040108.2(MLH3):c.4011+15T>G rs139032600 0.00031
NM_001040108.2(MLH3):c.3137G>A (p.Arg1046Gln) rs201303087 0.00018
NM_001040108.2(MLH3):c.2638C>G (p.Leu880Val) rs201453923 0.00010
NM_001040108.2(MLH3):c.873T>G (p.Asn291Lys) rs767413852 0.00009
NM_001040108.2(MLH3):c.2000G>C (p.Gly667Ala) rs200093225 0.00004
NM_001040108.2(MLH3):c.3676G>A (p.Ala1226Thr) rs747817741 0.00003
NM_001040108.2(MLH3):c.443T>C (p.Val148Ala) rs1484161045 0.00003
NM_001040108.2(MLH3):c.278G>A (p.Arg93Gln) rs781779034 0.00002
NM_001040108.2(MLH3):c.132G>T (p.Arg44Ser)
NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr) rs148409389
NM_001040108.2(MLH3):c.2021dup (p.Asn674fs) rs767782578
NM_001040108.2(MLH3):c.2799del (p.Val934fs)
NM_001040108.2(MLH3):c.885del (p.His296fs) rs1431264077

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