List of variants in gene CTNNA1 reported as benign by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.2220G>A (p.Ser740=)	rs1059110	0.32259
NM_001903.5(CTNNA1):c.1143+8G>C	rs288028	0.26126
NM_001903.5(CTNNA1):c.540A>C (p.Leu180=)	rs11552054	0.02707
NM_001903.5(CTNNA1):c.2226C>G (p.Val742=)	rs11552052	0.02031
NM_001903.5(CTNNA1):c.546T>G (p.Pro182=)	rs28363395	0.01185
NM_001903.5(CTNNA1):c.1390-11A>G	rs28363461	0.01143
NM_001903.5(CTNNA1):c.1405C>T (p.Leu469=)	rs28363462	0.01143
NM_001903.5(CTNNA1):c.2343A>G (p.Gln781=)	rs75050399	0.00996
NM_001903.5(CTNNA1):c.618G>C (p.Gln206His)	rs150893072	0.00414
NM_001903.5(CTNNA1):c.655C>T (p.Pro219Ser)	rs28363406	0.00259
NM_001903.5(CTNNA1):c.1748-16G>C	rs187293176	0.00254
NM_001903.5(CTNNA1):c.2013G>A (p.Ala671=)	rs28363488	0.00226
NM_001903.5(CTNNA1):c.1167C>T (p.His389=)	rs61736921	0.00225
NM_001903.5(CTNNA1):c.589-5T>C	rs186236339	0.00200
NM_001903.5(CTNNA1):c.1845C>T (p.Ser615=)	rs150965493	0.00178
NM_001903.5(CTNNA1):c.536C>T (p.Ala179Val)	rs28363394	0.00153
NM_001903.5(CTNNA1):c.301+20T>G	rs201543087	0.00098
NM_001903.5(CTNNA1):c.963C>T (p.Asp321=)	rs61736922	0.00073
NM_001903.5(CTNNA1):c.1899+18A>G	rs562041100	0.00058
NM_001903.5(CTNNA1):c.2514C>T (p.Val838=)	rs371058611	0.00058
NM_001903.5(CTNNA1):c.1782C>T (p.Ala594=)	rs142503438	0.00044
NM_001903.5(CTNNA1):c.2532A>G (p.Gln844=)	rs148289936	0.00042
NM_001903.5(CTNNA1):c.1310C>T (p.Ala437Val)	rs138782455	0.00031
NM_001903.5(CTNNA1):c.2298T>C (p.His766=)	rs764185931	0.00013
NM_001903.5(CTNNA1):c.2307C>T (p.Asp769=)	rs200857725	0.00004
NM_001903.5(CTNNA1):c.1329T>C (p.Asn443=)	rs775346533	0.00003
NM_001903.5(CTNNA1):c.2304C>T (p.Pro768=)	rs147022694	0.00003
NM_001903.5(CTNNA1):c.1747+20C>G	rs762799349	0.00002
NM_001903.5(CTNNA1):c.858+16G>A	rs778958561	0.00001
NM_001903.5(CTNNA1):c.1297-11dup
NM_001903.5(CTNNA1):c.1546+18del	rs1311087730
NM_001903.5(CTNNA1):c.1546+18dup
NM_001903.5(CTNNA1):c.2010+21del	rs1427926823
NM_001903.5(CTNNA1):c.2010+21dup	rs1427926823
NM_001903.5(CTNNA1):c.588+4_588+5del	rs147724289
NM_001903.5(CTNNA1):c.770A>G (p.Asn257Ser)	rs78627784

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