"PreventionGenetics, part of Exact Sciences"[submitter] AND "IRAK1"[ge - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2239348	NM_001569.4(IRAK1):c.1924G>A (p.Val642Met)	IRAK1 (V642M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2661779	NM_001569.4(IRAK1):c.1855G>A (p.Gly619Ser)	IRAK1 (G540S +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3037138	NM_001569.4(IRAK1):c.1641C>T (p.Tyr547=)	IRAK1	Single nucleotide variant (synonymous variant)	IRAK1-related disorder	GLikely benign
Select item 3031203	NM_001569.4(IRAK1):c.1195G>C (p.Gly399Arg)	IRAK1 (G399R +1 more)	Single nucleotide variant (missense variant)	IRAK1-related disorder	GUncertain significance
Select item 2661780	NM_001569.4(IRAK1):c.1128C>T (p.Ser376=)	IRAK1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 770829	NM_001569.4(IRAK1):c.1104C>T (p.Ala368=)	IRAK1	Single nucleotide variant (synonymous variant)	IRAK1-related disorder +1 more	GBenign/Likely benign
Select item 3040466	NM_001569.4(IRAK1):c.1098C>T (p.Arg366=)	IRAK1	Single nucleotide variant (synonymous variant)	IRAK1-related disorder	GLikely benign
Select item 3035914	NM_001569.4(IRAK1):c.1096C>T (p.Arg366Cys)	IRAK1 (R366C +1 more)	Single nucleotide variant (missense variant)	IRAK1-related disorder	GLikely benign
Select item 3054486	NM_001569.4(IRAK1):c.909+9A>G	IRAK1	Single nucleotide variant (intron variant)	IRAK1-related disorder	GLikely benign
Select item 3047572	NM_001569.4(IRAK1):c.729+10G>A	IRAK1	Single nucleotide variant (intron variant)	IRAK1-related disorder	GLikely benign
Select item 3032046	NM_001569.4(IRAK1):c.726G>A (p.Lys242=)	IRAK1	Single nucleotide variant (synonymous variant)	IRAK1-related disorder	GLikely benign
Select item 3029208	NM_001569.4(IRAK1):c.639G>A (p.Ser213=)	IRAK1	Single nucleotide variant (synonymous variant)	IRAK1-related disorder	GLikely benign
Select item 3053955	NM_001569.4(IRAK1):c.390G>C (p.Trp130Cys)	IRAK1 (W130C +1 more)	Single nucleotide variant (missense variant)	IRAK1-related disorder	GUncertain significance
Select item 786442	NM_001569.4(IRAK1):c.361A>C (p.Ile121Leu)	IRAK1, LOC130068849 (I121L)	Single nucleotide variant (missense variant)	IRAK1-related disorder +1 more	GBenign/Likely benign
Select item 3051065	NM_001569.4(IRAK1):c.338C>T (p.Thr113Ile)	IRAK1, LOC130068849 (T113I +1 more)	Single nucleotide variant (missense variant)	IRAK1-related disorder	GBenign
Select item 3038674	NM_001569.4(IRAK1):c.137-8C>A	IRAK1	Single nucleotide variant (synonymous variant +1 more)	IRAK1-related disorder	GLikely benign