List of variants in gene CD3G 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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000073.3(CD3G):c.*308G>A	rs73018291	0.02465
NM_000073.3(CD3G):c.79+10A>G	rs115851096	0.00266
NM_000073.3(CD3G):c.-17G>T	rs145293635	0.00124
NM_000073.3(CD3G):c.56G>A (p.Gly19Asp)	rs146393315	0.00075
NM_000073.3(CD3G):c.33C>G (p.Ile11Met)	rs143990986	0.00063
NM_000073.3(CD3G):c.*551C>T	rs45614033	0.00040
NM_000073.3(CD3G):c.*216C>A	rs200727417	0.00025
NM_000073.3(CD3G):c.511T>C (p.Tyr171His)	rs148191859	0.00024
NM_000073.3(CD3G):c.496C>A (p.Arg166=)	rs201529449	0.00022
NM_000073.3(CD3G):c.*141G>A	rs199668856	0.00013
NM_000073.3(CD3G):c.*500G>A	rs886047743	0.00008
NM_000073.3(CD3G):c.32T>C (p.Ile11Thr)	rs201006956	0.00007
NM_000073.3(CD3G):c.*112C>T	rs201272612	0.00006
NM_000073.3(CD3G):c.*253G>A	rs200106650	0.00006
NM_000073.3(CD3G):c.40A>G (p.Ile14Val)	rs377262966	0.00004
NM_000073.3(CD3G):c.497G>A (p.Arg166Gln)	rs764084817	0.00003
NM_000073.3(CD3G):c.*617G>T	rs1048944200	0.00002
NM_000073.3(CD3G):c.467A>G (p.Asn156Ser)	rs772803529	0.00002
NM_000073.3(CD3G):c.484C>A (p.Pro162Thr)	rs200624053	0.00002
NM_000073.3(CD3G):c.521T>C (p.Leu174Pro)	rs200685479	0.00002
NM_000073.3(CD3G):c.79+4G>A	rs1226309530	0.00002
NM_000073.3(CD3G):c.*363C>T	rs1044606855	0.00001
NM_000073.3(CD3G):c.458T>C (p.Leu153Pro)	rs1948410884	0.00001
NM_000073.3(CD3G):c.*426T>G	rs199632748
NM_000073.3(CD3G):c.*450T>G	rs200498090
NM_000073.3(CD3G):c.*650C>T	rs201175995
NM_000073.3(CD3G):c.11G>T (p.Gly4Val)	rs1483357286
NM_000073.3(CD3G):c.16G>C (p.Gly6Arg)	rs1481255896
NM_000073.3(CD3G):c.37G>A (p.Ala13Thr)	rs1948336348
NM_000073.3(CD3G):c.38C>T (p.Ala13Val)	rs1430979560
NM_000073.3(CD3G):c.41T>A (p.Ile14Asn)	rs1948336501
NM_000073.3(CD3G):c.466A>C (p.Asn156His)	rs1948410922
NM_000073.3(CD3G):c.529A>G (p.Asn177Asp)	rs2134072775
NM_000073.3(CD3G):c.55+11_55+23delinsGGCTATCATTCTTCTTCAAGGTAAGGGCCTTC
NM_000073.3(CD3G):c.79+3A>G	rs1948381958

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