"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "BICC1"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2719220	NM_001080512.3(BICC1):c.21C>T (p.Pro7=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2787162	NM_001080512.3(BICC1):c.26A>T (p.Tyr9Phe)	BICC1 (Y9F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1934585	NM_001080512.3(BICC1):c.28C>T (p.Leu10=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2992958	NM_001080512.3(BICC1):c.32C>G (p.Ala11Gly)	BICC1 (A11G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1383883	NM_001080512.3(BICC1):c.41C>T (p.Ser14Leu)	BICC1 (S14L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2017880	NM_001080512.3(BICC1):c.46C>A (p.Pro16Thr)	BICC1 (P16T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2782401	NM_001080512.3(BICC1):c.121C>T (p.Leu41=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2066224	NM_001080512.3(BICC1):c.131C>T (p.Pro44Leu)	BICC1 (P44L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2194261	NM_001080512.3(BICC1):c.171A>G (p.Lys57=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868359	NM_001080512.3(BICC1):c.181A>G (p.Met61Val)	BICC1 (M61V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1571190	NM_001080512.3(BICC1):c.191-18G>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1933239	NM_001080512.3(BICC1):c.207A>G (p.Lys69=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2088367	NM_001080512.3(BICC1):c.237G>A (p.Lys79=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2955429	NM_001080512.3(BICC1):c.237+8G>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2139140	NM_001080512.3(BICC1):c.288C>T (p.Ile96=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2063098	NM_001080512.3(BICC1):c.312C>G (p.Pro104=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2769545	NM_001080512.3(BICC1):c.387+14A>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 71078	NM_001080512.3(BICC1):c.444C>T (p.Ile148=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1946532	NM_001080512.3(BICC1):c.547-3T>C	BICC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2183691	NM_001080512.3(BICC1):c.549A>G (p.Val183=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2080767	NM_001080512.3(BICC1):c.553A>G (p.Ile185Val)	BICC1 (I185V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2904207	NM_001080512.3(BICC1):c.600+7A>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1934161	NM_001080512.3(BICC1):c.600+15C>G	BICC1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1625728	NM_001080512.3(BICC1):c.601-18C>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2200362	NM_001080512.3(BICC1):c.601-7A>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2052280	NM_001080512.3(BICC1):c.616G>A (p.Val206Met)	BICC1 (V206M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1206085	NM_001080512.3(BICC1):c.637A>G (p.Ile213Val)	BICC1 (I213V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2416779	NM_001080512.3(BICC1):c.656C>T (p.Pro219Leu)	BICC1 (P219L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2019353	NM_001080512.3(BICC1):c.707A>C (p.Asn236Thr)	BICC1 (N236T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 745084	NM_001080512.3(BICC1):c.738A>C (p.Arg246=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3016378	NM_001080512.3(BICC1):c.775A>G (p.Asn259Asp)	BICC1 (N259D)	Single nucleotide variant (missense variant)	Renal dysplasia, cystic, susceptibility to +2 more	GUncertain significance
Select item 1613202	NM_001080512.3(BICC1):c.796-14C>A	BICC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1930195	NM_001080512.3(BICC1):c.796-13C>T	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1943791	NM_001080512.3(BICC1):c.796-6T>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2145086	NM_001080512.3(BICC1):c.826G>T (p.Ala276Ser)	BICC1 (A276S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 786158	NM_001080512.3(BICC1):c.846T>C (p.Ala282=)	BICC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2009478	NM_001080512.3(BICC1):c.858C>T (p.Ser286=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1975369	NM_001080512.3(BICC1):c.863A>T (p.Gln288Leu)	BICC1 (Q288L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2779992	NM_001080512.3(BICC1):c.894T>C (p.Phe298=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1312347	NM_001080512.3(BICC1):c.974A>G (p.Asn325Ser)	BICC1 (N325S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2893123	NM_001080512.3(BICC1):c.990T>C (p.Ser330=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2710043	NM_001080512.3(BICC1):c.991A>G (p.Thr331Ala)	BICC1 (T331A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 383742	NM_001080512.3(BICC1):c.994G>A (p.Val332Ile)	BICC1 (V332I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1601688	NM_001080512.3(BICC1):c.1038A>G (p.Gln346=)	BICC1	Single nucleotide variant (synonymous variant)	Renal dysplasia, cystic, susceptibility to +1 more	GBenign
Select item 2846737	NM_001080512.3(BICC1):c.1048-19C>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1908512	NM_001080512.3(BICC1):c.1048-14G>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1544689	NM_001080512.3(BICC1):c.1065G>A (p.Val355=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2068962	NM_001080512.3(BICC1):c.1134T>C (p.Leu378=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045754	NM_001080512.3(BICC1):c.1148G>C (p.Ser383Thr)	BICC1 (S383T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2176158	NM_001080512.3(BICC1):c.1150A>G (p.Ile384Val)	BICC1 (I384V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1940896	NM_001080512.3(BICC1):c.1179+12G>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1617650	NM_001080512.3(BICC1):c.1180-4A>G	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2842176	NM_001080512.3(BICC1):c.1242_1366+680del	BICC1	Deletion (splice donor variant)	not provided	GUncertain significance
Select item 2843128	NM_001080512.3(BICC1):c.1245C>T (p.Leu415=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1992096	NM_001080512.3(BICC1):c.1270A>G (p.Ile424Val)	BICC1 (I424V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2346938	NM_001080512.3(BICC1):c.1271T>G (p.Ile424Arg)	BICC1 (I424R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2969493	NM_001080512.3(BICC1):c.1305C>T (p.Ala435=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2852868	NM_001080512.3(BICC1):c.1311G>A (p.Leu437=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1186376	NM_001080512.3(BICC1):c.1366+4T>C	BICC1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 2123611	NM_001080512.3(BICC1):c.1367-20T>C	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967914	NM_001080512.3(BICC1):c.1399A>G (p.Thr467Ala)	BICC1 (T467A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175444	NM_001080512.3(BICC1):c.1425G>C (p.Leu475Phe)	BICC1 (L475F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2149833	NM_001080512.3(BICC1):c.1457A>G (p.Gln486Arg)	BICC1 (Q486R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1968235	NM_001080512.3(BICC1):c.1507G>A (p.Ala503Thr)	BICC1 (A503T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2284094	NM_001080512.3(BICC1):c.1615G>A (p.Gly539Arg)	BICC1 (G539R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2358311	NM_001080512.3(BICC1):c.1622C>G (p.Thr541Arg)	BICC1 (T541R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1895854	NM_001080512.3(BICC1):c.1639C>G (p.Pro547Ala)	BICC1 (P547A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1980230	NM_001080512.3(BICC1):c.1659T>G (p.Asp553Glu)	BICC1 (D553E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1973759	NM_001080512.3(BICC1):c.1675A>G (p.Met559Val)	BICC1 (M559V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2896894	NM_001080512.3(BICC1):c.1683C>T (p.Thr561=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2995850	NM_001080512.3(BICC1):c.1717C>T (p.His573Tyr)	BICC1 (H573Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2987449	NM_001080512.3(BICC1):c.1725+17A>T	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2706707	NM_001080512.3(BICC1):c.1731A>G (p.Pro577=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2141175	NM_001080512.3(BICC1):c.1779G>A (p.Val593=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2118482	NM_001080512.3(BICC1):c.1795G>A (p.Gly599Arg)	BICC1 (G599R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094639	NM_001080512.3(BICC1):c.1854T>C (p.Thr618=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2397980	NM_001080512.3(BICC1):c.1859G>A (p.Gly620Asp)	BICC1 (G620D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1383427	NM_001080512.3(BICC1):c.1859G>T (p.Gly620Val)	BICC1 (G620V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2397836	NM_001080512.3(BICC1):c.1861T>G (p.Cys621Gly)	BICC1 (C621G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1952411	NM_001080512.3(BICC1):c.1970G>A (p.Arg657Lys)	BICC1 (R657K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2064075	NM_001080512.3(BICC1):c.1996A>G (p.Thr666Ala)	BICC1 (T666A)	Single nucleotide variant (missense variant)	Renal dysplasia, cystic, susceptibility to +2 more	GUncertain significance
Select item 2183790	NM_001080512.3(BICC1):c.2010C>G (p.His670Gln)	BICC1 (H670Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1636766	NM_001080512.3(BICC1):c.2016-19C>T	BICC1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1548216	NM_001080512.3(BICC1):c.2016-18C>T	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1899153	NM_001080512.3(BICC1):c.2016-12C>A	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 768366	NM_001080512.3(BICC1):c.2016-8T>C	BICC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 716212	NM_001080512.3(BICC1):c.2046A>T (p.Glu682Asp)	BICC1 (E682D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1526374	NM_001080512.3(BICC1):c.2047C>T (p.Leu683=)	BICC1	Single nucleotide variant (synonymous variant)	Renal dysplasia, cystic, susceptibility to +1 more	GBenign/Likely benign
Select item 2085268	NM_001080512.3(BICC1):c.2055T>G (p.Ala685=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1556879	NM_001080512.3(BICC1):c.2058C>T (p.Thr686=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1570101	NM_001080512.3(BICC1):c.2100C>T (p.Arg700=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1202567	NM_001080512.3(BICC1):c.2132A>C (p.Asn711Thr)	BICC1 (N711T)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1937848	NM_001080512.3(BICC1):c.2158C>T (p.Arg720Trp)	BICC1 (R720W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1661982	NM_001080512.3(BICC1):c.2159G>A (p.Arg720Gln)	BICC1 (R720Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1898909	NM_001080512.3(BICC1):c.2181+15A>T	BICC1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2414858	NM_001080512.3(BICC1):c.2190C>T (p.Asp730=)	BICC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2817147	NM_001080512.3(BICC1):c.2221G>A (p.Ala741Thr)	BICC1 (A741T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1990277	NM_001080512.3(BICC1):c.2221+19A>G	BICC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3010934	NM_001080512.3(BICC1):c.2235A>G (p.Lys745=)	BICC1, LOC126860938	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2722550	NM_001080512.3(BICC1):c.2247G>A (p.Thr749=)	BICC1, LOC126860938	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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