List of variants in gene CD3G reported as likely benign 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000073.3(CD3G):c.56G>A (p.Gly19Asp)	rs146393315	0.00075
NM_000073.3(CD3G):c.511T>C (p.Tyr171His)	rs148191859	0.00024
NM_000073.3(CD3G):c.36G>A (p.Leu12=)	rs181713283	0.00015
NM_000073.3(CD3G):c.56-17C>A	rs201370125	0.00004
NM_000073.3(CD3G):c.55+14A>G	rs1221658161	0.00001
NM_000073.3(CD3G):c.55+16G>A	rs768957947	0.00001
NM_000073.3(CD3G):c.55+8C>T	rs1342882807	0.00001
NM_000073.3(CD3G):c.72A>C (p.Ser24=)	rs768284919	0.00001
NM_000073.3(CD3G):c.12G>A (p.Gly4=)
NM_000073.3(CD3G):c.440-19_440-18del	rs1322603987
NM_000073.3(CD3G):c.484-13C>T
NM_000073.3(CD3G):c.484-17T>A
NM_000073.3(CD3G):c.484-4C>A	rs1565523004
NM_000073.3(CD3G):c.484-4C>G	rs1565523004
NM_000073.3(CD3G):c.55+11A>G
NM_000073.3(CD3G):c.55+12C>G
NM_000073.3(CD3G):c.55+15G>A
NM_000073.3(CD3G):c.55+19T>C
NM_000073.3(CD3G):c.56-17C>T	rs201370125
NM_000073.3(CD3G):c.56-5T>C	rs1248241886
NM_000073.3(CD3G):c.69G>A (p.Gln23=)	rs2134068299
NM_000073.3(CD3G):c.72A>T (p.Ser24=)	rs768284919

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