List of variants in gene MLH3 studied for carcinoma

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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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.2482G>T (p.Glu828Ter)	rs587776622
NM_001040108.2(MLH3):c.2799del (p.Val934fs)
NM_001040108.2(MLH3):c.3034G>A (p.Ala1012Thr)	rs1057518875

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