"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DDX41"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2811517	NM_016222.4(DDX41):c.1868G>A (p.Ter623=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2877539	NM_016222.4(DDX41):c.1854C>T (p.Ser618=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2762106	NM_016222.4(DDX41):c.1836G>A (p.Lys612=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1337686	NM_016222.4(DDX41):c.1827C>T (p.Ile609=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 2958373	NM_016222.4(DDX41):c.1794C>T (p.Leu598=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1720235	NM_016222.4(DDX41):c.1789A>G (p.Lys597Glu)	DDX41 (K471E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2186096	NM_016222.4(DDX41):c.1755C>T (p.Cys585=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2969582	NM_016222.4(DDX41):c.1740C>T (p.Arg580=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2442413	NM_016222.4(DDX41):c.1739G>A (p.Arg580His)	DDX41 (R454H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1980118	NM_016222.4(DDX41):c.1733-3C>T	DDX41	Single nucleotide variant (intron variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2992817	NM_016222.4(DDX41):c.1733-17del	DDX41	Deletion (intron variant)	not provided	GLikely benign
Select item 1908592	NM_016222.4(DDX41):c.1733-18_1733-17del	DDX41	Deletion (intron variant)	not provided	GLikely benign
Select item 2792789	NM_016222.4(DDX41):c.1733-20C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1896836	NM_016222.4(DDX41):c.1732+19C>A	DDX41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2868469	NM_016222.4(DDX41):c.1732+14G>A	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1905854	NM_016222.4(DDX41):c.1732+13C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881112	NM_016222.4(DDX41):c.1732+6T>G	DDX41	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1954657	NM_016222.4(DDX41):c.1704C>T (p.Cys568=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2005966	NM_016222.4(DDX41):c.1693G>T (p.Val565Leu)	DDX41 (V439L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1982762	NM_016222.4(DDX41):c.1684G>A (p.Val562Met)	DDX41 (V562M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 434912	NM_016222.4(DDX41):c.1683C>T (p.Pro561=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 3018084	NM_016222.4(DDX41):c.1680G>A (p.Pro560=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2794854	NM_016222.4(DDX41):c.1679C>T (p.Pro560Leu)	DDX41 (P560L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 977491	NM_016222.4(DDX41):c.1668G>T (p.Lys556Asn)	DDX41 (K430N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 434913	NM_016222.4(DDX41):c.1665C>T (p.Ala555=)	DDX41	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1337040	NM_016222.4(DDX41):c.1650G>A (p.Ala550=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2712709	NM_016222.4(DDX41):c.1644C>T (p.Leu548=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1337816	NM_016222.4(DDX41):c.1622-3C>T	DDX41	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1336019	NM_016222.4(DDX41):c.1622-5C>G	DDX41	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 1248286	NM_016222.4(DDX41):c.1622-20C>G	DDX41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2100229	NM_016222.4(DDX41):c.1621+18G>A	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2190208	NM_016222.4(DDX41):c.1621+9G>A	DDX41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2993156	NM_016222.4(DDX41):c.1621+6T>C	DDX41	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1901278	NM_016222.4(DDX41):c.1621+3G>A	DDX41	Single nucleotide variant (intron variant)	DDX41-related hematologic malignancy predisposition syndrome +1 more	GUncertain significance
Select item 2030306	NM_016222.4(DDX41):c.1611C>T (p.Asn537=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1928156	NM_016222.4(DDX41):c.1602C>T (p.Thr534=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2783996	NM_016222.4(DDX41):c.1599T>G (p.Thr533=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2500222	NM_016222.4(DDX41):c.1589G>A (p.Gly530Asp)	DDX41 (G404D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 978204	NM_016222.4(DDX41):c.1586_1587del (p.Thr529fs)	DDX41 (T403fs +1 more)	Microsatellite (frameshift variant)	DDX41-related hematologic malignancy predisposition syndrome +1 more	GPathogenic
Select item 2779370	NM_016222.4(DDX41):c.1585A>G (p.Thr529Ala)	DDX41 (T529A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1901432	NM_016222.4(DDX41):c.1577C>T (p.Ser526Leu)	DDX41 (S400L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 224634	NM_016222.4(DDX41):c.1574G>A (p.Arg525His)	DDX41 (R525H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2835738	NM_016222.4(DDX41):c.1570G>A (p.Gly524Arg)	DDX41 (G398R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2197018	NM_016222.4(DDX41):c.1569C>T (p.Thr523=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3014347	NM_016222.4(DDX41):c.1565G>A (p.Arg522His)	DDX41 (R522H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2580837	NM_016222.4(DDX41):c.1563C>T (p.Gly521=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 2760377	NM_016222.4(DDX41):c.1550-4G>C	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2982992	NM_016222.4(DDX41):c.1550-11_1550-9del	DDX41	Deletion (intron variant)	not provided	GLikely benign
Select item 2854783	NM_016222.4(DDX41):c.1549+19A>G	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1908897	NM_016222.4(DDX41):c.1549+15C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1969870	NM_016222.4(DDX41):c.1549+9C>G	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2044946	NM_016222.4(DDX41):c.1549+8C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1337840	NM_016222.4(DDX41):c.1547A>G (p.Tyr516Cys)	DDX41 (Y390C +1 more)	Single nucleotide variant (missense variant)	DDX41-related disorder +3 more	GUncertain significance
Select item 2864398	NM_016222.4(DDX41):c.1538T>C (p.Ile513Thr)	DDX41 (I387T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1910010	NM_016222.4(DDX41):c.1532A>G (p.Glu511Gly)	DDX41 (E385G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1981975	NM_016222.4(DDX41):c.1528C>T (p.Pro510Ser)	DDX41 (P384S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1907787	NM_016222.4(DDX41):c.1509C>T (p.His503=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1312513	NM_016222.4(DDX41):c.1496dup (p.Ala500fs)	DDX41 (A374fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2674795	NM_016222.4(DDX41):c.1496del (p.Pro499fs)	DDX41 (P373fs +1 more)	Deletion (frameshift variant)	DDX41-related hematologic malignancy predisposition syndrome +1 more	GPathogenic/Likely pathogenic
Select item 726954	NM_016222.4(DDX41):c.1479C>T (p.Ser493=)	DDX41	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1313184	NM_016222.4(DDX41):c.1471G>A (p.Val491Ile)	DDX41 (V365I +1 more)	Single nucleotide variant (missense variant)	DDX41-related hematologic malignancy predisposition syndrome +2 more	GUncertain significance
Select item 1337229	NM_016222.4(DDX41):c.1470C>T (p.Asp490=)	DDX41	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 2828163	NM_016222.4(DDX41):c.1465A>G (p.Thr489Ala)	DDX41 (T363A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2784023	NM_016222.4(DDX41):c.1441G>A (p.Gly481Ser)	DDX41 (G481S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 978208	NM_016222.4(DDX41):c.1436G>A (p.Arg479Gln)	DDX41 (R353Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 2111172	NM_016222.4(DDX41):c.1431del (p.Phe478fs)	DDX41 (F478fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2578173	NM_016222.4(DDX41):c.1415C>T (p.Thr472Ile)	DDX41 (T346I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2071639	NM_016222.4(DDX41):c.1411C>T (p.Arg471Trp)	DDX41 (R471W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2762854	NM_016222.4(DDX41):c.1400-16G>A	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1904433	NM_016222.4(DDX41):c.1400-19_1400-16del	DDX41	Deletion (intron variant)	not provided	GLikely benign
Select item 3022426	NM_016222.4(DDX41):c.1399+18A>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2005078	NM_016222.4(DDX41):c.1399+17C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1337873	NM_016222.4(DDX41):c.1399+10G>A	DDX41	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2446598	NM_016222.4(DDX41):c.1395C>T (p.Gly465=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1922261	NM_016222.4(DDX41):c.1377C>T (p.Ala459=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2989780	NM_016222.4(DDX41):c.1368G>C (p.Gly456=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1179260	NM_016222.4(DDX41):c.1354C>T (p.Leu452=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2170953	NM_016222.4(DDX41):c.1347C>T (p.His449=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969006	NM_016222.4(DDX41):c.1338C>T (p.Asp446=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1312353	NM_016222.4(DDX41):c.1334_1336del (p.Val445del)	DDX41 (V319del +1 more)	Deletion (inframe_deletion)	not provided	GConflicting classifications of pathogenicity
Select item 1337424	NM_016222.4(DDX41):c.1332C>T (p.Asp444=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1698327	NM_016222.4(DDX41):c.1308C>T (p.Leu436=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 2781869	NM_016222.4(DDX41):c.1303-3C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2705819	NM_016222.4(DDX41):c.1303-7C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993077	NM_016222.4(DDX41):c.1303-17T>G	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2180159	NM_016222.4(DDX41):c.1302+8C>T	DDX41	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1313715	NM_016222.4(DDX41):c.1301C>T (p.Pro434Leu)	DDX41 (P308L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1336306	NM_016222.4(DDX41):c.1299G>A (p.Pro433=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2853869	NM_016222.4(DDX41):c.1298C>T (p.Pro433Leu)	DDX41 (P433L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2169291	NM_016222.4(DDX41):c.1296C>G (p.Pro432=)	DDX41	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1336572	NM_016222.4(DDX41):c.1283T>C (p.Leu428Pro)	DDX41 (L302P +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1919893	NM_016222.4(DDX41):c.1276G>A (p.Glu426Lys)	DDX41 (E426K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1904793	NM_016222.4(DDX41):c.1275C>T (p.Leu425=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2704359	NM_016222.4(DDX41):c.1273C>T (p.Leu425Phe)	DDX41 (L425F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2891037	NM_016222.4(DDX41):c.1266G>A (p.Val422=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2895705	NM_016222.4(DDX41):c.1254G>A (p.Glu418=)	DDX41	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2958500	NM_016222.4(DDX41):c.1242T>C (p.Tyr414=)	DDX41	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 1916143	NM_016222.4(DDX41):c.1234G>A (p.Val412Ile)	DDX41 (V286I +1 more)	Single nucleotide variant (missense variant)	DDX41-related hematologic malignancy predisposition syndrome +1 more	GUncertain significance
Select item 434914	NM_016222.4(DDX41):c.1233G>A (p.Glu411=)	DDX41	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1723764	NM_016222.4(DDX41):c.1231-5G>A	DDX41	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance

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