ClinVar Miner

List of variants in gene combination COL4A3, MFF-DT reported by Myriad Genetics, Inc.

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Gene type:
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Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_000091.5(COL4A3):c.1295C>T (p.Pro432Leu) rs534253913 0.00002
NM_000091.5(COL4A3):c.2197G>T (p.Gly733Ter) rs2071839316 0.00001
NM_000091.5(COL4A3):c.2452G>A (p.Gly818Arg) rs868002181 0.00001
NM_000091.5(COL4A3):c.1015_1016insTGAAA (p.Gly339fs)
NM_000091.5(COL4A3):c.1042_1043delinsT (p.Asp348fs)
NM_000091.5(COL4A3):c.1066G>T (p.Glu356Ter)
NM_000091.5(COL4A3):c.1188G>A (p.Trp396Ter) rs1348174898
NM_000091.5(COL4A3):c.1213G>T (p.Glu405Ter) rs2070736908
NM_000091.5(COL4A3):c.1361del (p.Pro454fs)
NM_000091.5(COL4A3):c.1408G>T (p.Gly470Ter) rs2070901479
NM_000091.5(COL4A3):c.1507A>T (p.Arg503Ter)
NM_000091.5(COL4A3):c.151A>T (p.Lys51Ter) rs2068937789
NM_000091.5(COL4A3):c.1531G>T (p.Gly511Ter) rs921768118
NM_000091.5(COL4A3):c.1572dup (p.Pro525fs)
NM_000091.5(COL4A3):c.1615G>T (p.Glu539Ter) rs2071189852
NM_000091.5(COL4A3):c.1645C>T (p.Gln549Ter)
NM_000091.5(COL4A3):c.1662_1663del (p.Asp555fs)
NM_000091.5(COL4A3):c.1682_1685del (p.Gln561fs)
NM_000091.5(COL4A3):c.1729A>T (p.Lys577Ter)
NM_000091.5(COL4A3):c.1747A>T (p.Lys583Ter) rs920504687
NM_000091.5(COL4A3):c.1767_1773del (p.Ser589fs)
NM_000091.5(COL4A3):c.1855G>T (p.Gly619Ter) rs773515249
NM_000091.5(COL4A3):c.1879del (p.Gln627fs)
NM_000091.5(COL4A3):c.2076_2077del (p.Glu693fs)
NM_000091.5(COL4A3):c.2170G>T (p.Gly724Ter)
NM_000091.5(COL4A3):c.2192T>A (p.Leu731Ter)
NM_000091.5(COL4A3):c.2444dup (p.Ala816fs)
NM_000091.5(COL4A3):c.2456_2457insACTGTCTCTTA (p.Pro820fs)
NM_000091.5(COL4A3):c.2590C>T (p.Gln864Ter) rs2072046147
NM_000091.5(COL4A3):c.2591_2592insT (p.Gln864fs)
NM_000091.5(COL4A3):c.2602G>T (p.Gly868Ter)
NM_000091.5(COL4A3):c.2617A>T (p.Arg873Ter) rs2072047738
NM_000091.5(COL4A3):c.2673_2676delinsATTTTCGA (p.Gly892fs)
NM_000091.5(COL4A3):c.280G>T (p.Gly94Ter) rs2069240492
NM_000091.5(COL4A3):c.2830_2831delinsG (p.Pro944fs)
NM_000091.5(COL4A3):c.2834C>A (p.Ser945Ter) rs2072184526
NM_000091.5(COL4A3):c.2870del (p.Pro957fs)
NM_000091.5(COL4A3):c.2950A>T (p.Lys984Ter)
NM_000091.5(COL4A3):c.2953G>T (p.Gly985Ter) rs2072530756
NM_000091.5(COL4A3):c.304dup (p.Ser102fs)
NM_000091.5(COL4A3):c.3176C>A (p.Ser1059Ter) rs2072651666
NM_000091.5(COL4A3):c.3206del (p.Pro1069fs)
NM_000091.5(COL4A3):c.3292G>T (p.Gly1098Ter)
NM_000091.5(COL4A3):c.3312AAGTCCTGG[1] (p.1105SPG[1]) rs756539994
NM_000091.5(COL4A3):c.3327_3330del (p.Gly1110fs)
NM_000091.5(COL4A3):c.3362T>A (p.Leu1121Ter) rs2072936269
NM_000091.5(COL4A3):c.3370A>T (p.Lys1124Ter) rs2072936529
NM_000091.5(COL4A3):c.3373G>T (p.Gly1125Ter) rs2072936636
NM_000091.5(COL4A3):c.3561_3562del (p.Gln1188fs)
NM_000091.5(COL4A3):c.3565G>T (p.Gly1189Ter) rs2072983130
NM_000091.5(COL4A3):c.3647del (p.Gly1216fs)
NM_000091.5(COL4A3):c.3749del (p.Pro1250fs)
NM_000091.5(COL4A3):c.3915del (p.Arg1306fs)
NM_000091.5(COL4A3):c.3952A>T (p.Lys1318Ter) rs2073363435
NM_000091.5(COL4A3):c.3968_3970delinsTT (p.Asn1323fs)
NM_000091.5(COL4A3):c.4004del (p.Pro1335fs)
NM_000091.5(COL4A3):c.4036G>T (p.Gly1346Ter) rs2073400756
NM_000091.5(COL4A3):c.4054A>T (p.Lys1352Ter) rs2073401408
NM_000091.5(COL4A3):c.4100del (p.Gly1367fs)
NM_000091.5(COL4A3):c.4207G>T (p.Gly1403Ter)
NM_000091.5(COL4A3):c.4240A>T (p.Lys1414Ter)
NM_000091.5(COL4A3):c.4270G>T (p.Gly1424Ter) rs2073567181
NM_000091.5(COL4A3):c.4298del (p.Gly1433fs)
NM_000091.5(COL4A3):c.4307del (p.Gly1436fs)
NM_000091.5(COL4A3):c.4429C>T (p.Gln1477Ter)
NM_000091.5(COL4A3):c.4515C>A (p.Cys1505Ter) rs2073628823
NM_000091.5(COL4A3):c.4559C>A (p.Ser1520Ter)
NM_000091.5(COL4A3):c.4566G>A (p.Trp1522Ter) rs2073630720
NM_000091.5(COL4A3):c.4615A>T (p.Arg1539Ter)
NM_000091.5(COL4A3):c.4625_4626del (p.Glu1542fs)
NM_000091.5(COL4A3):c.4634_4635del (p.Ile1545fs)
NM_000091.5(COL4A3):c.4710T>A (p.Cys1570Ter)
NM_000091.5(COL4A3):c.570del (p.Pro191fs)
NM_000091.5(COL4A3):c.615del (p.Pro206fs)
NM_000091.5(COL4A3):c.643A>T (p.Lys215Ter)
NM_000091.5(COL4A3):c.700_701del (p.Leu234fs)
NM_000091.5(COL4A3):c.737_738insATGTGTATAAGAGACA (p.Val246_Thr247insCysValTer)
NM_000091.5(COL4A3):c.803dup (p.Glu269fs)
NM_000091.5(COL4A3):c.894del (p.Lys298fs) rs2070145822
NM_000091.5(COL4A3):c.94_95del (p.Val32fs)
NM_000091.5(COL4A3):c.991C>T (p.Gln331Ter) rs768527987

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