List of variants in gene SLC1A3 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.*174del	rs538321546	0.00368
NM_004172.5(SLC1A3):c.*1206G>A	rs530235885	0.00146
NM_004172.5(SLC1A3):c.*761G>A	rs182371422	0.00034
NM_004172.5(SLC1A3):c.*1605T>A	rs182194574	0.00028
NM_004172.5(SLC1A3):c.*1554T>G	rs986025125	0.00023
NM_004172.5(SLC1A3):c.*733G>A	rs542557347	0.00021
NM_004172.5(SLC1A3):c.*1445A>T	rs764991205	0.00017
NM_004172.5(SLC1A3):c.*843C>T	rs111315626	0.00011
NM_004172.5(SLC1A3):c.*516T>C	rs971147962	0.00006
NM_004172.5(SLC1A3):c.1284A>C (p.Thr428=)	rs200947079	0.00006
NM_004172.5(SLC1A3):c.*439T>A	rs1742662576	0.00004
NM_004172.5(SLC1A3):c.-205G>A	rs202216601	0.00003
NM_004172.5(SLC1A3):c.1269C>T (p.Phe423=)	rs758802146	0.00003
NM_004172.5(SLC1A3):c.955G>A (p.Val319Met)	rs753136358	0.00003
NM_004172.5(SLC1A3):c.*1160T>C	rs886060548	0.00001
NM_004172.5(SLC1A3):c.-20C>A	rs759949496	0.00001
NM_004172.5(SLC1A3):c.1167C>T (p.Phe389=)	rs372548093	0.00001
NM_004172.5(SLC1A3):c.212A>G (p.Tyr71Cys)	rs573483474	0.00001
NM_004172.5(SLC1A3):c.28A>G (p.Lys10Glu)	rs754763002	0.00001
NM_004172.5(SLC1A3):c.297T>G (p.Leu99=)	rs754571819	0.00001
NM_004172.5(SLC1A3):c.374T>C (p.Val125Ala)	rs764799721	0.00001
NM_004172.5(SLC1A3):c.641T>C (p.Ile214Thr)	rs761385978	0.00001
NM_004172.5(SLC1A3):c.825C>T (p.Asn275=)	rs201765665	0.00001
NM_004172.4(SLC1A3):c.-280C>T	rs886060542
NM_004172.5(SLC1A3):c.*1229A>G	rs886060549
NM_004172.5(SLC1A3):c.*1533G>A	rs1742717006
NM_004172.5(SLC1A3):c.*313dup	rs886060544
NM_004172.5(SLC1A3):c.*440A>G	rs1742662690
NM_004172.5(SLC1A3):c.*617dup	rs886060546
NM_004172.5(SLC1A3):c.*955C>A	rs1742686704
NM_004172.5(SLC1A3):c.1188C>T (p.Thr396=)	rs1309265652
NM_004172.5(SLC1A3):c.601G>A (p.Val201Met)	rs748235513
NM_004172.5(SLC1A3):c.625C>G (p.Leu209Val)	rs146815724
NM_004172.5(SLC1A3):c.860+9T>C	rs886060543
NM_004172.5(SLC1A3):c.897G>C (p.Gly299=)	rs768627283

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