List of variants in gene THOC2 reported as likely pathogenic for developmental disorder of mental health

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001081550.2(THOC2):c.149A>C (p.Tyr50Ser)	rs1603326578
NM_001081550.2(THOC2):c.1844G>A (p.Cys615Tyr)	rs2147667154
NM_001081550.2(THOC2):c.1942G>T (p.Ala648Ser)	rs2047665750
NM_001081550.2(THOC2):c.2087C>T (p.Thr696Ile)	rs1556024875
NM_001081550.2(THOC2):c.2695T>C (p.Tyr899His)	rs2147617004
NM_001081550.2(THOC2):c.3305A>G (p.Tyr1102Cys)	rs2047177327
NM_001081550.2(THOC2):c.3503+4A>C	rs1556015437
NM_001081550.2(THOC2):c.3559C>T (p.His1187Tyr)	rs1556014935
NM_001081550.2(THOC2):c.4450-2A>G	rs1556005930

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