ClinVar Miner

List of variants in gene KRIT1 reported as benign

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_194454.3(KRIT1):c.989+63C>G rs2027950 0.57036
NM_194454.3(KRIT1):c.1818+146A>G rs74603220 0.10873
NM_194454.3(KRIT1):c.1980A>G (p.Val660=) rs11542682 0.10861
NM_194456.1(KRIT1):c.*1385A>G rs62467792 0.09950
NM_194454.3(KRIT1):c.729+240G>T rs73407588 0.03646
NM_194456.1(KRIT1):c.*1444T>G rs10240962 0.02684
NM_194454.3(KRIT1):c.*272G>A rs28502064 0.02669
NM_194454.3(KRIT1):c.*320C>T rs112567410 0.02314
NM_194454.3(KRIT1):c.486-193T>C rs75654928 0.01703
NM_194454.3(KRIT1):c.-356G>A rs117169559 0.00762
NM_194454.3(KRIT1):c.*141C>T rs117325194 0.00554
NM_194456.1(KRIT1):c.*1363T>G rs148980420 0.00355
NM_194454.3(KRIT1):c.2044A>C (p.Lys682Gln) rs138763545 0.00264
NM_194454.3(KRIT1):c.1095A>G (p.Gly365=) rs143710815 0.00238
NM_194454.3(KRIT1):c.-43C>T rs193080208 0.00220
NM_194454.3(KRIT1):c.846-5dup rs373763254 0.00219
NM_194454.3(KRIT1):c.1245T>G (p.Ile415Met) rs41278788 0.00194
NM_194456.1(KRIT1):c.*1750C>T rs188612683 0.00188
NM_194454.3(KRIT1):c.1140G>A (p.Thr380=) rs140009885 0.00187
NM_194456.1(KRIT1):c.*1702A>G rs192818018 0.00163
NM_194454.3(KRIT1):c.*132T>G rs572414111 0.00138
NM_194454.3(KRIT1):c.*137del rs543954194 0.00138
NM_194454.3(KRIT1):c.1819-12G>C rs199748245 0.00097
NM_194454.3(KRIT1):c.77G>A (p.Arg26Gln) rs34358665 0.00097
NM_194454.3(KRIT1):c.1146+8A>T rs182762651 0.00093
NM_194454.3(KRIT1):c.2046G>A (p.Lys682=) rs144960332 0.00080
NM_194454.3(KRIT1):c.1782A>G (p.Ala594=) rs145605400 0.00054
NM_194454.3(KRIT1):c.2085T>A (p.Thr695=) rs149437256 0.00051
NM_194454.3(KRIT1):c.302G>T (p.Gly101Val) rs147568834 0.00044
NM_194454.3(KRIT1):c.1412-9G>A rs199932606 0.00043
NM_194454.3(KRIT1):c.*46G>A rs369227523 0.00029
NM_194454.3(KRIT1):c.-2-7T>C rs550533414 0.00029
NM_194454.3(KRIT1):c.845+10C>T rs372125478 0.00026
NM_194454.3(KRIT1):c.1326C>G (p.Thr442=) rs150912644 0.00023
NM_194454.3(KRIT1):c.*234G>A rs574668355 0.00016
NM_194454.3(KRIT1):c.444T>C (p.His148=) rs746035680 0.00014
NM_194454.3(KRIT1):c.1809T>C (p.His603=) rs149754162 0.00011
NM_194454.3(KRIT1):c.1063C>T (p.Leu355Phe) rs182763805 0.00004
NM_194454.3(KRIT1):c.846-15C>T rs527439925 0.00003
NM_194454.3(KRIT1):c.*57G>A rs529937203 0.00001
NM_194454.3(KRIT1):c.-312A>G rs538102163 0.00001
NM_194454.3(KRIT1):c.1139C>T (p.Thr380Met) rs533696377 0.00001
NM_194454.3(KRIT1):c.262+68A>G rs1554536465 0.00001
NM_194456.1(KRIT1):c.*1530T>C rs75182503 0.00001
NM_194454.3(KRIT1):c.*378dup rs34910226
NM_194454.3(KRIT1):c.1147-20dup
NM_194454.3(KRIT1):c.1255-296del rs568078150
NM_194454.3(KRIT1):c.1411+181G>A rs112410984
NM_194454.3(KRIT1):c.1564-316A>T rs10271533
NM_194454.3(KRIT1):c.485+65G>C rs17164451
NM_194454.3(KRIT1):c.730-93A>G rs73407587
NM_194456.1(KRIT1):c.*1335T>C rs17164414

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