ClinVar Miner

List of variants in gene combination LOC129933707, MSH6 studied for not provided

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.260+22C>G rs55927047 0.13136
NM_000179.3(MSH6):c.257C>T (p.Thr86Ile) rs768444916 0.00002
NM_000179.3(MSH6):c.246T>C (p.Pro82=) rs786201527 0.00001
NM_000179.3(MSH6):c.251C>T (p.Ala84Val) rs878853717 0.00001
NM_000179.3(MSH6):c.260+3A>G rs1553408474 0.00001
NM_000179.3(MSH6):c.260+7G>A rs774479750 0.00001
NM_000179.3(MSH6):c.-4_259del (p.Met1*) rs2103930283
NM_000179.3(MSH6):c.248C>A (p.Ala83Asp) rs876661197
NM_000179.3(MSH6):c.248C>G (p.Ala83Gly) rs876661197
NM_000179.3(MSH6):c.253C>T (p.Pro85Ser) rs779664343
NM_000179.3(MSH6):c.254C>T (p.Pro85Leu) rs1060502945
NM_000179.3(MSH6):c.255C>A (p.Pro85=) rs587779242
NM_000179.3(MSH6):c.255C>G (p.Pro85=) rs587779242
NM_000179.3(MSH6):c.255del (p.Thr86fs) rs1064793183
NM_000179.3(MSH6):c.256A>C (p.Thr86Pro) rs1553408451
NM_000179.3(MSH6):c.257C>G (p.Thr86Ser) rs768444916
NM_000179.3(MSH6):c.259A>T (p.Ser87Cys) rs1064793939
NM_000179.3(MSH6):c.260+2T>A rs1553408469
NM_000179.3(MSH6):c.260+2_260+3delinsAG rs1064794075
NM_000179.3(MSH6):c.260G>C (p.Ser87Thr) rs1114167734

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