ClinVar Miner

List of variants in gene KRIT1 reported as likely benign by Invitae

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_194454.3(KRIT1):c.77G>A (p.Arg26Gln) rs34358665 0.00097
NM_194454.3(KRIT1):c.2207C>T (p.Ser736Leu) rs151059782 0.00081
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.235A>G (p.Ile79Val) rs116801031 0.00038
NM_194454.3(KRIT1):c.845+10C>T rs372125478 0.00026
NM_194454.3(KRIT1):c.587C>G (p.Ala196Gly) rs549707288 0.00024
NM_194454.3(KRIT1):c.1326C>G (p.Thr442=) rs150912644 0.00023
NM_194454.3(KRIT1):c.1914A>G (p.Ala638=) rs146106391 0.00019
NM_194454.3(KRIT1):c.510A>G (p.Gln170=) rs200684252 0.00018
NM_194454.3(KRIT1):c.444T>C (p.His148=) rs746035680 0.00014
NM_194454.3(KRIT1):c.845+9T>G rs140152251 0.00014
NM_194454.3(KRIT1):c.1752C>T (p.Ile584=) rs148836047 0.00011
NM_194454.3(KRIT1):c.2068T>C (p.Leu690=) rs370766145 0.00009
NM_194454.3(KRIT1):c.582A>G (p.Ala194=) rs369744043 0.00008
NM_194454.3(KRIT1):c.1355G>A (p.Arg452His) rs201272513 0.00006
NM_194454.3(KRIT1):c.264A>G (p.Gly88=) rs201877439 0.00006
NM_194454.3(KRIT1):c.1428A>G (p.Pro476=) rs781533650 0.00003
NM_194454.3(KRIT1):c.1134A>T (p.Pro378=) rs752464613 0.00002
NM_194454.3(KRIT1):c.1176A>G (p.Pro392=) rs538610091 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.276A>G (p.Val92=) rs573853526 0.00001
NM_194454.3(KRIT1):c.675A>T (p.Ala225=) rs770622492 0.00001
NM_194454.3(KRIT1):c.729+8T>C rs1208375976 0.00001
NM_194454.3(KRIT1):c.885C>T (p.Ser295=) rs761571988 0.00001
NM_194454.3(KRIT1):c.1023A>G (p.Leu341=)
NM_194454.3(KRIT1):c.103-7A>T
NM_194454.3(KRIT1):c.126T>C (p.Ile42=)
NM_194454.3(KRIT1):c.1299T>G (p.Ser433=)
NM_194454.3(KRIT1):c.1326C>T (p.Thr442=) rs150912644
NM_194454.3(KRIT1):c.1329A>G (p.Thr443=)
NM_194454.3(KRIT1):c.1359C>T (p.Leu453=) rs1584881048
NM_194454.3(KRIT1):c.1377A>G (p.Gln459=)
NM_194454.3(KRIT1):c.1384A>G (p.Thr462Ala)
NM_194454.3(KRIT1):c.1411+14T>C rs1450901829
NM_194454.3(KRIT1):c.1411+20_1411+24del rs886038758
NM_194454.3(KRIT1):c.1419A>C (p.Gln473His) rs748732288
NM_194454.3(KRIT1):c.1440C>T (p.Pro480=) rs1321821110
NM_194454.3(KRIT1):c.1480T>C (p.Leu494=)
NM_194454.3(KRIT1):c.1680A>G (p.Gln560=)
NM_194454.3(KRIT1):c.168G>A (p.Thr56=)
NM_194454.3(KRIT1):c.1731-14A>C
NM_194454.3(KRIT1):c.1860C>T (p.His620=)
NM_194454.3(KRIT1):c.2007C>T (p.Leu669=) rs1584794752
NM_194454.3(KRIT1):c.2026-20del rs763882887
NM_194454.3(KRIT1):c.213C>T (p.Tyr71=)
NM_194454.3(KRIT1):c.228C>T (p.Thr76=)
NM_194454.3(KRIT1):c.30A>G (p.Ala10=)
NM_194454.3(KRIT1):c.387C>T (p.Cys129=) rs2131676285
NM_194454.3(KRIT1):c.477C>T (p.Ala159=) rs1584988756
NM_194454.3(KRIT1):c.485+12C>T
NM_194454.3(KRIT1):c.485+13G>A
NM_194454.3(KRIT1):c.485+13G>T
NM_194454.3(KRIT1):c.525A>G (p.Pro175=) rs753361614
NM_194454.3(KRIT1):c.567T>C (p.Asn189=)
NM_194454.3(KRIT1):c.594A>G (p.Glu198=)
NM_194454.3(KRIT1):c.612C>T (p.Asn204=)
NM_194454.3(KRIT1):c.615A>G (p.Ser205=) rs2131662377
NM_194454.3(KRIT1):c.636A>G (p.Ala212=)
NM_194454.3(KRIT1):c.730-4del
NM_194454.3(KRIT1):c.845+10C>G rs372125478
NM_194454.3(KRIT1):c.918T>C (p.Arg306=) rs2131642409
NM_194454.3(KRIT1):c.990-22GTTT[4]
NM_194454.3(KRIT1):c.990-5T>C

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