"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRAK1"[ge - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 734589	NM_001042646.3(TRAK1):c.33C>G (p.Val11=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2052551	NM_001042646.3(TRAK1):c.175G>A (p.Asp59Asn)	TRAK1 (D59N)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 753302	NM_001042646.3(TRAK1):c.186C>T (p.Tyr62=)	TRAK1	Single nucleotide variant (synonymous variant +2 more)	TRAK1-related disorder +1 more	GLikely benign
Select item 2653702	NM_001042646.3(TRAK1):c.286+23939A>G	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3043408	NM_001042646.3(TRAK1):c.287-16460C>A	TRAK1	Single nucleotide variant (5 prime UTR variant +1 more)	TRAK1-related disorder	GLikely benign
Select item 1013468	NM_001042646.3(TRAK1):c.327T>C (p.Tyr109=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1666680	NM_001042646.3(TRAK1):c.481-10G>T	TRAK1	Single nucleotide variant (intron variant)	TRAK1-related disorder +1 more	GBenign
Select item 2081938	NM_001042646.3(TRAK1):c.545C>T (p.Ala182Val)	TRAK1 (A108V +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2742017	NM_001042646.3(TRAK1):c.582-7C>T	TRAK1	Single nucleotide variant (intron variant)	TRAK1-related disorder +1 more	GLikely benign
Select item 2061248	NM_001042646.3(TRAK1):c.702G>A (p.Leu234=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2851432	NM_001042646.3(TRAK1):c.903C>T (p.Cys301=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 2696678	NM_001042646.3(TRAK1):c.976-8G>T	TRAK1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1615167	NM_001042646.3(TRAK1):c.1162T>C (p.Leu388=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	TRAK1-related disorder +1 more	GLikely benign
Select item 3033966	NM_001042646.3(TRAK1):c.1190+4C>T	TRAK1	Single nucleotide variant (intron variant)	TRAK1-related disorder	GLikely benign
Select item 3033354	NM_001042646.3(TRAK1):c.1331C>G (p.Thr444Ser)	TRAK1 (T340S +3 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder	GUncertain significance
Select item 734533	NM_001042646.3(TRAK1):c.1451C>T (p.Pro484Leu)	TRAK1 (P410L +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GLikely benign
Select item 1701455	NM_001042646.3(TRAK1):c.1549G>A (p.Glu517Lys)	TRAK1 (E413K +3 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder +1 more	GBenign
Select item 2722168	NM_001042646.3(TRAK1):c.1669A>T (p.Thr557Ser)	TRAK1 (T499S +3 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder +1 more	GBenign
Select item 1896294	NM_001042646.3(TRAK1):c.1744+11G>T	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3024989	NM_001042646.3(TRAK1):c.1744+44C>T	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2636519	NM_001042646.3(TRAK1):c.1744+75G>A	TRAK1 (A533T)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder	GUncertain significance
Select item 1649699	NM_001042646.3(TRAK1):c.1860C>T (p.Asp620=)	TRAK1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2634169	NM_001042646.3(TRAK1):c.1963+258C>T	TRAK1 (R667C +2 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder	GUncertain significance
Select item 1370337	NM_001042646.3(TRAK1):c.2054G>A (p.Arg685Gln)	TRAK1 (R560Q +4 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1594964	NM_001042646.3(TRAK1):c.2056G>T (p.Val686Phe)	TRAK1 (V561F +4 more)	Single nucleotide variant (missense variant +1 more)	TRAK1-related disorder +1 more	GLikely benign
Select item 2197868	NM_001042646.3(TRAK1):c.2262C>T (p.Tyr754=)	TRAK1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 775198	NM_001042646.3(TRAK1):c.2348C>G (p.Pro783Arg)	TRAK1 (P658R +4 more)	Single nucleotide variant (missense variant +2 more)	TRAK1-related disorder +1 more	GBenign/Likely benign
Select item 2969515	NM_001042646.3(TRAK1):c.2529C>T (p.Leu843=)	TRAK1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 1281419	NM_001042646.3(TRAK1):c.2799T>C (p.Pro933=)	TRAK1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign
Select item 1335510	NM_001042646.3(TRAK1):c.2856A>G (p.Leu952=)	TRAK1	Single nucleotide variant (synonymous variant +2 more)	TRAK1-related disorder +1 more	GLikely benign

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Items: 30