List of variants in gene ZAP70 reported as uncertain significance for immune system disorder

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_001079.4(ZAP70):c.1082+8C>T	rs55933862	0.00271
NM_001079.4(ZAP70):c.1737-3C>T	rs56249179	0.00100
NM_001079.4(ZAP70):c.1467C>T (p.Asp489=)	rs55997284	0.00094
NM_001079.4(ZAP70):c.1289+10G>A	rs200538234	0.00088
NM_001079.4(ZAP70):c.1624-12C>T	rs201487332	0.00086
NM_001079.4(ZAP70):c.-133C>T	rs201616095	0.00081
NM_001079.4(ZAP70):c.1025T>C (p.Ile342Thr)	rs142702703	0.00058
NM_001079.4(ZAP70):c.*328C>T	rs201790312	0.00049
NM_001079.4(ZAP70):c.1656C>T (p.Ile552=)	rs150096962	0.00037
NM_001079.4(ZAP70):c.1645A>G (p.Met549Val)	rs150950017	0.00036
NM_001079.4(ZAP70):c.*11C>A	rs200035333	0.00031
NM_001079.4(ZAP70):c.981C>G (p.Asp327Glu)	rs201605654	0.00014
NM_001079.3(ZAP70):c.-217G>A	rs201824270	0.00013
NM_001079.4(ZAP70):c.*274G>A	rs55721260	0.00012
NM_001079.4(ZAP70):c.828G>A (p.Thr276=)	rs200797733	0.00010
NM_001079.4(ZAP70):c.1617C>T (p.Pro539=)	rs189807102	0.00007
NM_001079.4(ZAP70):c.606C>T (p.Leu202=)	rs199943332	0.00006
NM_001079.4(ZAP70):c.988C>T (p.Leu330Phe)	rs371574765	0.00005
NM_001079.4(ZAP70):c.837+6T>C	rs199639189	0.00004
NM_001079.4(ZAP70):c.920C>T (p.Pro307Leu)	rs201386206	0.00004
NM_001079.4(ZAP70):c.*161G>A	rs886056486	0.00003
NM_001079.4(ZAP70):c.1832C>T (p.Thr611Ile)	rs371359430	0.00003
NM_001079.4(ZAP70):c.729G>A (p.Ala243=)	rs754793583	0.00003
NM_001079.4(ZAP70):c.692C>T (p.Thr231Met)	rs141613906	0.00002
NM_001079.4(ZAP70):c.790+6G>A	rs200018109	0.00002
NM_001079.4(ZAP70):c.*228G>A	rs199863225	0.00001
NM_001079.4(ZAP70):c.*48C>T	rs1411918610	0.00001
NM_001079.4(ZAP70):c.1078C>T (p.Arg360Cys)	rs781463009	0.00001
NM_001079.4(ZAP70):c.1083-3C>A	rs199890589	0.00001
NM_001079.4(ZAP70):c.1392C>A (p.Ala464=)	rs1289751768	0.00001
NM_001079.4(ZAP70):c.403-3T>C	rs202193449	0.00001
NM_001079.4(ZAP70):c.440C>T (p.Pro147Leu)	rs368446882	0.00001
NM_001079.4(ZAP70):c.655G>A (p.Gly219Ser)	rs200295650	0.00001
NM_001079.4(ZAP70):c.-81T>G	rs200416837
NM_001079.4(ZAP70):c.156C>T (p.His52=)	rs138447206
NM_001079.4(ZAP70):c.1737-7C>T	rs1573292727
NM_001079.4(ZAP70):c.199G>T (p.Gly67Cys)	rs745420613
NM_001079.4(ZAP70):c.467C>G (p.Thr156Arg)	rs1266171275
NM_001079.4(ZAP70):c.516G>A (p.Glu172=)	rs886056485
NM_001079.4(ZAP70):c.80C>A (p.Ala27Glu)	rs373708142
NM_001079.4(ZAP70):c.939C>T (p.Ser313=)

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