ClinVar Miner

List of variants in gene FASLG reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_000639.3(FASLG):c.426G>C (p.Glu142Asp) rs138441486 0.00088
NM_000639.3(FASLG):c.108G>A (p.Val36=) rs140595317 0.00054
NM_000639.3(FASLG):c.395-15C>G rs370579312 0.00038
NM_000639.3(FASLG):c.174G>A (p.Pro58=) rs372411796 0.00034
NM_000639.3(FASLG):c.280T>G (p.Leu94Val) rs56302117 0.00033
NM_000639.3(FASLG):c.796C>T (p.Leu266=) rs35178418 0.00029
NM_000639.3(FASLG):c.828C>T (p.Phe276=) rs144105303 0.00026
NC_000001.11:g.172658929A>G rs895958192 0.00021
NM_000639.3(FASLG):c.394+14C>T rs371078346 0.00009
NM_000639.3(FASLG):c.153G>A (p.Pro51=) rs147380045 0.00008
NM_000639.3(FASLG):c.204G>A (p.Leu68=) rs951438902 0.00008
NM_000639.3(FASLG):c.278C>T (p.Ala93Val) rs758796005 0.00005
NM_000639.3(FASLG):c.*32T>C rs775421228 0.00004
NM_000639.3(FASLG):c.-16T>C rs781373207 0.00004
NM_000639.3(FASLG):c.176C>T (p.Pro59Leu) rs375737004 0.00004
NM_000639.3(FASLG):c.270T>C (p.Val90=) rs765440709 0.00003
NM_000639.3(FASLG):c.624C>T (p.Ser208=) rs761180254 0.00003
NM_000639.3(FASLG):c.144A>G (p.Pro48=) rs55664927 0.00002
NM_000639.3(FASLG):c.180G>A (p.Pro60=) rs753980291 0.00001
NM_000639.3(FASLG):c.243G>T (p.Leu81=) rs760651511 0.00001
NM_000639.3(FASLG):c.348+12G>A rs776445206 0.00001
NM_000639.3(FASLG):c.349-45G>T rs778330321 0.00001
NM_000639.3(FASLG):c.395-9A>G rs373975939 0.00001
NM_000639.3(FASLG):c.451+8T>A rs372021169 0.00001
NM_000639.3(FASLG):c.452-12G>A rs759351686 0.00001
NM_000639.3(FASLG):c.561G>A (p.Gly187=) rs1267175575 0.00001
NM_000639.3(FASLG):c.579C>T (p.Ser193=) rs374974805 0.00001
NM_000639.3(FASLG):c.678G>A (p.Glu226=) rs752708760 0.00001
NM_000639.3(FASLG):c.135A>G (p.Pro45=)
NM_000639.3(FASLG):c.174G>C (p.Pro58=)
NM_000639.3(FASLG):c.207A>G (p.Pro69=) rs769398033
NM_000639.3(FASLG):c.209C>G (p.Pro70Arg) rs1317103645
NM_000639.3(FASLG):c.210C>T (p.Pro70=)
NM_000639.3(FASLG):c.213G>A (p.Leu71=)
NM_000639.3(FASLG):c.225G>A (p.Gly75=) rs761614632
NM_000639.3(FASLG):c.241C>T (p.Leu81=)
NM_000639.3(FASLG):c.279C>T (p.Ala93=)
NM_000639.3(FASLG):c.295C>T (p.Leu99=)
NM_000639.3(FASLG):c.312C>T (p.Leu104=)
NM_000639.3(FASLG):c.321A>G (p.Leu107=)
NM_000639.3(FASLG):c.348+11C>T
NM_000639.3(FASLG):c.348+14C>T
NM_000639.3(FASLG):c.348+9G>A
NM_000639.3(FASLG):c.349-13T>C
NM_000639.3(FASLG):c.349-16C>T
NM_000639.3(FASLG):c.351T>G (p.Ser117=)
NM_000639.3(FASLG):c.394+16C>A
NM_000639.3(FASLG):c.394+17A>C
NM_000639.3(FASLG):c.395-13C>G
NM_000639.3(FASLG):c.405T>C (p.Ser135=)
NM_000639.3(FASLG):c.411C>A (p.Pro137=)
NM_000639.3(FASLG):c.451+11G>A
NM_000639.3(FASLG):c.451+12G>A
NM_000639.3(FASLG):c.452-11A>T
NM_000639.3(FASLG):c.453C>A (p.Gly151=)
NM_000639.3(FASLG):c.498T>C (p.Tyr166=)
NM_000639.3(FASLG):c.522G>A (p.Val174=)
NM_000639.3(FASLG):c.537T>C (p.Gly179=) rs2101810574
NM_000639.3(FASLG):c.540C>T (p.Gly180=)
NM_000639.3(FASLG):c.552T>C (p.Asn184=)
NM_000639.3(FASLG):c.615G>T (p.Leu205=) rs2101810642
NM_000639.3(FASLG):c.666G>A (p.Leu222=) rs2101810683
NM_000639.3(FASLG):c.702T>C (p.Thr234=)
NM_000639.3(FASLG):c.708G>A (p.Gly236=)
NM_000639.3(FASLG):c.720C>T (p.Ala240=)
NM_000639.3(FASLG):c.72C>A (p.Ala24=) rs182516315
NM_000639.3(FASLG):c.780C>T (p.Asn260=)
NM_000639.3(FASLG):c.822G>A (p.Thr274=)
NM_000639.3(FASLG):c.822G>T (p.Thr274=) rs199500307
NM_001302746.1(FASLG):c.-187_-186GA[4] rs55853758

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