List of variants in gene SRC reported as not provided by Psychiatry Genetics Yale University

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_198291.3(SRC):c.1263G>A (p.Ala421=)	rs367543245	0.00006
NM_198291.3(SRC):c.12C>T (p.Asn4=)	rs367543237	0.00006
NM_198291.3(SRC):c.1323C>A (p.Arg441=)	rs367543246	0.00006
NM_198291.3(SRC):c.727C>T (p.Arg243Cys)	rs367543241	0.00006
NM_198291.3(SRC):c.846C>T (p.Gly282=)	rs367543242	0.00006
NM_198291.3(SRC):c.1387C>T (p.Arg463Trp)	rs367543247	0.00001
NM_198291.3(SRC):c.61G>A (p.Ala21Thr)	rs367543238	0.00001
NM_198291.3(SRC):c.642C>T (p.Gly214=)	rs367543240	0.00001
NM_198291.3(SRC):c.1200C>T (p.Asn400=)	rs367543243
NM_198291.3(SRC):c.1239C>T (p.Leu413=)	rs367543244
NM_198291.3(SRC):c.1474G>A (p.Glu492Lys)	rs367543248
NM_198291.3(SRC):c.85G>T (p.Gly29Trp)	rs367543239

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