C1336839[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 93567	NM_000245.4(MET):c.144G>A (p.Ala48=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 93573	NM_000245.4(MET):c.390C>T (p.Leu130=)	MET	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GBenign
Select item 41627	NM_000245.4(MET):c.504G>T (p.Glu168Asp)	MET (E168D)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 93578	NM_000245.4(MET):c.534C>T (p.Ser178=)	MET	Single nucleotide variant (synonymous variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +5 more	GBenign
Select item 454255	NM_000245.4(MET):c.690G>A (p.Thr230=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +2 more	GBenign/Likely benign
Select item 215795	NM_000245.4(MET):c.939G>A (p.Val313=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +3 more	GLikely benign
Select item 93565	NM_000245.4(MET):c.1085T>C (p.Met362Thr)	MET (M362T)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +4 more	GBenign
Select item 41611	NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	MET (N375S)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign
Select item 93566	NM_000245.4(MET):c.1131C>T (p.Ile377=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 135957	NM_000245.4(MET):c.1191C>T (p.Cys397=)	MET	Single nucleotide variant (synonymous variant +1 more)	Papillary renal cell carcinoma type 1 +3 more	GBenign/Likely benign
Select item 246622	NM_000245.4(MET):c.1278C>T (p.Arg426=)	MET	Single nucleotide variant (synonymous variant +1 more)	not specified +4 more	GLikely benign
Select item 454202	NM_000245.4(MET):c.1881T>C (p.Gly627=)	MET	Single nucleotide variant (synonymous variant)	not provided +3 more	GLikely benign
Select item 93569	NM_000245.4(MET):c.1944A>G (p.Gln648=)	MET	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 358689	NM_000245.4(MET):c.1965+14T>C	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma +1 more	GBenign/Likely benign
Select item 134645	NM_000245.4(MET):c.3522T>C (p.His1174=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma +3 more	GBenign/Likely benign
Select item 358693	NM_000245.4(MET):c.3523-12C>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma +4 more	GBenign/Likely benign
Select item 93574	NM_000245.4(MET):c.3858C>T (p.Asp1286=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma +5 more	GBenign
Select item 93575	NM_000245.4(MET):c.4017G>A (p.Ala1339=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma +5 more	GBenign
Select item 93576	NM_000245.4(MET):c.4092G>A (p.Pro1364=)	MET	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign
Select item 12364	NM_000546.6(TP53):c.844C>T (p.Arg282Trp)	TP53 (R282W +3 more)	Single nucleotide variant (missense variant)	not provided +10 more	GPathogenic/Likely pathogenic OOncogenic
Select item 376667	NM_000546.6(TP53):c.374C>G (p.Thr125Arg)	TP53 (T125R +1 more)	Single nucleotide variant (missense variant)	Li-Fraumeni syndrome 1 +4 more	GPathogenic/Likely pathogenic OLikely oncogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 21