List of variants in gene SNTA1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.1147G>A (p.Val383Met)	rs767361112	0.00006
NM_003098.3(SNTA1):c.1015C>T (p.Arg339Cys)	rs138164106	0.00005
NM_003098.3(SNTA1):c.782C>T (p.Ala261Val)	rs139467962	0.00005
NM_003098.3(SNTA1):c.1180C>T (p.Arg394Cys)	rs567451585	0.00004
NM_003098.3(SNTA1):c.1340G>A (p.Arg447Gln)	rs752729935	0.00004
NM_003098.3(SNTA1):c.556G>A (p.Gly186Ser)	rs200755101	0.00004
NM_003098.3(SNTA1):c.992G>A (p.Arg331His)	rs575431717	0.00004
NM_003098.3(SNTA1):c.1309G>A (p.Glu437Lys)	rs371648806	0.00003
NM_003098.3(SNTA1):c.160G>C (p.Gly54Arg)	rs786205848	0.00003
NM_003098.3(SNTA1):c.817C>T (p.Pro273Ser)	rs750459988	0.00003
NM_003098.3(SNTA1):c.1106G>A (p.Arg369His)	rs1012069434	0.00002
NM_003098.3(SNTA1):c.1118G>A (p.Arg373His)	rs754648214	0.00002
NM_003098.3(SNTA1):c.1204C>T (p.Arg402Trp)	rs373387978	0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln)	rs771369802	0.00002
NM_003098.3(SNTA1):c.1388T>G (p.Leu463Arg)	rs188835994	0.00002
NM_003098.3(SNTA1):c.620G>A (p.Arg207Gln)	rs771180054	0.00002
NM_003098.3(SNTA1):c.668C>T (p.Ser223Leu)	rs779370807	0.00002
NM_003098.3(SNTA1):c.1021G>A (p.Ala341Thr)	rs754242619	0.00001
NM_003098.3(SNTA1):c.1425+1G>A	rs113809208	0.00001
NM_003098.3(SNTA1):c.1484C>T (p.Ser495Leu)	rs144006909	0.00001
NM_003098.3(SNTA1):c.1486G>C (p.Ala496Pro)	rs1463586615	0.00001
NM_003098.3(SNTA1):c.316C>T (p.Arg106Trp)	rs552509775	0.00001
NM_003098.3(SNTA1):c.403A>C (p.Ile135Leu)	rs756587722	0.00001
NM_003098.3(SNTA1):c.419G>C (p.Gly140Ala)	rs768194552	0.00001
NM_003098.3(SNTA1):c.497-5A>G	rs202178576	0.00001
NM_003098.3(SNTA1):c.526T>C (p.Phe176Leu)	rs781703999	0.00001
NM_003098.3(SNTA1):c.719C>T (p.Ser240Leu)	rs35168199	0.00001
NM_003098.3(SNTA1):c.759T>A (p.Asp253Glu)	rs759487225	0.00001
NM_003098.3(SNTA1):c.*412G>C	rs566401281
NM_003098.3(SNTA1):c.1003_1021dup (p.Ala341fs)	rs775891730
NM_003098.3(SNTA1):c.1244C>T (p.Thr415Met)	rs533902889
NM_003098.3(SNTA1):c.1283A>G (p.Asp428Gly)	rs1390997295
NM_003098.3(SNTA1):c.1498C>T (p.Arg500Cys)	rs786205426
NM_003098.3(SNTA1):c.370G>A (p.Asp124Asn)	rs1430826527

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