C1266144[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 242133	NM_177438.3(DICER1):c.5241G>A (p.Ser1747=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +4 more	GBenign/Likely benign
Select item 135513	NM_177438.3(DICER1):c.5095+13C>T	DICER1	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign
Select item 242125	NM_177438.3(DICER1):c.4899A>G (p.Val1633=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +2 more	GLikely benign
Select item 417121	NM_177438.3(DICER1):c.4807C>T (p.Leu1603=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 417101	NM_177438.3(DICER1):c.4796G>A (p.Arg1599Gln)	DICER1 (R1599Q)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GLikely benign
Select item 261925	NM_177438.3(DICER1):c.4680G>A (p.Ala1560=)	DICER1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 261924	NM_177438.3(DICER1):c.4407T>C (p.Leu1469=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +3 more	GBenign/Likely benign
Select item 315105	NM_177438.3(DICER1):c.4206+9G>T	DICER1	Single nucleotide variant (intron variant)	Euthyroid goiter +3 more	GBenign/Likely benign
Select item 220744	NM_177438.3(DICER1):c.3972G>A (p.Lys1324=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 315107	NM_177438.3(DICER1):c.3269+14G>A	DICER1	Single nucleotide variant (intron variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 242078	NM_177438.3(DICER1):c.3198T>C (p.Thr1066=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +4 more	GBenign
Select item 261921	NM_177438.3(DICER1):c.3033G>A (p.Ala1011=)	DICER1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 261920	NM_177438.3(DICER1):c.2997T>G (p.Leu999=)	DICER1	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 477116	NM_177438.3(DICER1):c.2718C>T (p.Arg906=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +2 more	GLikely benign
Select item 133967	NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr)	DICER1 (A872T)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GBenign FDA Recognized database
Select item 417102	NM_177438.3(DICER1):c.2613C>T (p.Asp871=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related condition +4 more	GLikely benign
Select item 417125	NM_177438.3(DICER1):c.2553G>A (p.Gln851=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +4 more	GConflicting classifications of pathogenicity
Select item 221128	NM_177438.3(DICER1):c.2370G>A (p.Arg790=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +7 more	GBenign
Select item 221180	NM_177438.3(DICER1):c.1935G>A (p.Pro645=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 242051	NM_177438.3(DICER1):c.1887G>A (p.Thr629=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +4 more	GBenign
Select item 220838	NM_177438.3(DICER1):c.1377-4T>G	DICER1	Single nucleotide variant (intron variant)	not provided +7 more	GBenign/Likely benign
Select item 417078	NM_177438.3(DICER1):c.1329C>T (p.Cys443=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related condition +3 more	GBenign/Likely benign
Select item 220595	NM_177438.3(DICER1):c.924C>T (p.Ala308=)	DICER1	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 133962	NM_177438.3(DICER1):c.20A>G (p.Gln7Arg)	DICER1 (Q7R)	Single nucleotide variant (missense variant)	Breast neoplasm +5 more	GConflicting classifications of pathogenicity

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Items: 24