List of variants in gene SPTAN1 reported as uncertain significance for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001130438.3(SPTAN1):c.6234C>T (p.Ala2078=)	rs147132904	0.00175
NM_001130438.3(SPTAN1):c.3042T>G (p.Gly1014=)	rs150870424	0.00028
NM_001130438.3(SPTAN1):c.6235G>A (p.Ala2079Thr)	rs377253398	0.00008
NM_001130438.3(SPTAN1):c.237+4C>T	rs371350283	0.00007
NM_001130438.3(SPTAN1):c.2224C>T (p.Arg742Cys)	rs780658554	0.00004
NM_001130438.3(SPTAN1):c.3673C>T (p.Arg1225Trp)	rs569997507	0.00004
NM_001130438.3(SPTAN1):c.3779A>G (p.Asn1260Ser)	rs552623597	0.00004
NM_001130438.3(SPTAN1):c.3156-10C>T	rs745910160	0.00003
NM_001130438.3(SPTAN1):c.4280G>A (p.Arg1427His)	rs762216368	0.00002
NM_001130438.3(SPTAN1):c.511A>G (p.Ile171Val)	rs771906889	0.00002
NM_001130438.3(SPTAN1):c.1502G>A (p.Ser501Asn)	rs1347944186	0.00001
NM_001130438.3(SPTAN1):c.2599G>A (p.Glu867Lys)	rs1339046005	0.00001
NM_001130438.3(SPTAN1):c.2645G>A (p.Arg882His)	rs1486021166	0.00001
NM_001130438.3(SPTAN1):c.3161G>A (p.Arg1054His)	rs561564501	0.00001
NM_001130438.3(SPTAN1):c.3358G>A (p.Gly1120Arg)	rs748698544	0.00001
NM_001130438.3(SPTAN1):c.3519+5G>T	rs915019884	0.00001
NM_001130438.3(SPTAN1):c.3579+3_3579+4dup	rs797046004	0.00001
NM_001130438.3(SPTAN1):c.649C>G (p.Gln217Glu)	rs756290749	0.00001
NM_001130438.3(SPTAN1):c.6764G>A (p.Arg2255His)	rs201693154	0.00001
NM_001130438.3(SPTAN1):c.1085+4C>T
NM_001130438.3(SPTAN1):c.3262G>A (p.Glu1088Lys)	rs780374369
NM_001130438.3(SPTAN1):c.363+1G>A	rs1554737064
NM_001130438.3(SPTAN1):c.6254T>C (p.Leu2085Pro)	rs1564315528
NM_001130438.3(SPTAN1):c.6273_6274delinsTT (p.Arg2092Cys)	rs796053333
NM_001130438.3(SPTAN1):c.6841C>A (p.Leu2281Ile)	rs1341044436
NM_001130438.3(SPTAN1):c.7014-16_7014-13delinsAGGT	rs796053336
NM_001130438.3(SPTAN1):c.862G>C (p.Ala288Pro)	rs796053298

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