"Genome-Nilou Lab"[submitter] AND "TRPA1"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1342276	NM_007332.3(TRPA1):c.3053A>G (p.His1018Arg)	MSC-AS1, TRPA1 (H1018R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1342277	NM_007332.3(TRPA1):c.2938-24C>G	MSC-AS1, TRPA1	Single nucleotide variant (intron variant)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1342278	NM_007332.3(TRPA1):c.2938-49T>G	MSC-AS1, TRPA1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1342279	NM_007332.3(TRPA1):c.2869-6C>A	MSC-AS1, TRPA1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1342280	NM_007332.3(TRPA1):c.1905+28C>T	MSC-AS1, TRPA1	Single nucleotide variant (intron variant)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1342281	NM_007332.3(TRPA1):c.1644+15C>T	MSC-AS1, TRPA1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1342282	NM_007332.3(TRPA1):c.1630C>T (p.Leu544=)	MSC-AS1, TRPA1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1342283	NM_007332.3(TRPA1):c.1530-22T>C	MSC-AS1, TRPA1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1342284	NM_007332.3(TRPA1):c.558A>C (p.Lys186Asn)	TRPA1 (K186N)	Single nucleotide variant (missense variant)	Familial episodic pain syndrome with predominantly upper body involvement +1 more	GBenign
Select item 1239453	NM_007332.3(TRPA1):c.375T>C (p.Asn125=)	TRPA1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign