ClinVar Miner

List of variants studied for Lynch syndrome; Mismatch repair cancer syndrome 4 by GenomeConnect - Invitae Patient Insights Network

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000535.7(PMS2):c.2012C>T (p.Thr671Met) rs587780046 0.00017
NM_000535.7(PMS2):c.857A>G (p.Asp286Gly) rs116788608 0.00011
NM_000535.7(PMS2):c.1714G>A (p.Ala572Thr) rs63751023 0.00009
NM_000535.7(PMS2):c.2559C>G (p.Ile853Met) rs371673459 0.00007
NM_000535.7(PMS2):c.883C>T (p.Arg295Trp) rs182246929 0.00003
NM_000535.7(PMS2):c.608C>G (p.Thr203Ser) rs779946576 0.00001
NM_000535.7(PMS2):c.1949C>T (p.Ala650Val) rs886062399

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