ClinVar Miner

List of variants in gene KRIT1 reported as likely benign for not provided

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_194456.1(KRIT1):c.*1363T>G rs148980420 0.00355
NM_194454.3(KRIT1):c.1095A>G (p.Gly365=) rs143710815 0.00238
NM_194454.3(KRIT1):c.1245T>G (p.Ile415Met) rs41278788 0.00194
NM_194454.3(KRIT1):c.1140G>A (p.Thr380=) rs140009885 0.00187
NM_194454.3(KRIT1):c.77G>A (p.Arg26Gln) rs34358665 0.00097
NM_194454.3(KRIT1):c.1782A>G (p.Ala594=) rs145605400 0.00054
NM_194454.3(KRIT1):c.845+10C>T rs372125478 0.00026
NM_194454.3(KRIT1):c.2068T>C (p.Leu690=) rs370766145 0.00016
NM_194454.3(KRIT1):c.1868G>A (p.Arg623His) rs143644029 0.00012
NM_194454.3(KRIT1):c.264A>G (p.Gly88=) rs201877439 0.00006
NM_194454.3(KRIT1):c.-346G>A rs1002702257 0.00001
NM_194454.3(KRIT1):c.1041T>C (p.Asn347=) rs373275660 0.00001
NM_194454.3(KRIT1):c.1306T>C (p.Leu436=) rs998452517 0.00001
NM_194454.3(KRIT1):c.1938A>G (p.Thr646=) rs369915828 0.00001
NM_194454.3(KRIT1):c.2160A>G (p.Lys720=) rs1178875536 0.00001
NM_194454.3(KRIT1):c.262+142T>G rs1485549584 0.00001
NM_194454.3(KRIT1):c.276A>G (p.Val92=) rs573853526 0.00001
NM_194454.3(KRIT1):c.1308G>A (p.Leu436=) rs1190790030
NM_194454.3(KRIT1):c.1359C>T (p.Leu453=) rs1584881048
NM_194454.3(KRIT1):c.1425A>G (p.Lys475=) rs1017236415
NM_194454.3(KRIT1):c.2007C>T (p.Leu669=) rs1584794752
NM_194454.3(KRIT1):c.477C>T (p.Ala159=) rs1584988756

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