List of variants in gene TCEANC2 reported by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_153035.3(TCEANC2):c.358A>G (p.Ile120Val)	rs745440627	0.00002
NM_153035.3(TCEANC2):c.359T>C (p.Ile120Thr)	rs200057608	0.00002
NM_153035.3(TCEANC2):c.251C>T (p.Thr84Ile)	rs762802716	0.00001
NM_153035.3(TCEANC2):c.329T>C (p.Phe110Ser)	rs1041676863	0.00001
NM_153035.3(TCEANC2):c.121G>A (p.Asp41Asn)	rs764125137
NM_153035.3(TCEANC2):c.23C>A (p.Thr8Lys)
NM_153035.3(TCEANC2):c.251C>G (p.Thr84Ser)
NM_153035.3(TCEANC2):c.349A>G (p.Arg117Gly)
NM_153035.3(TCEANC2):c.401A>G (p.Asn134Ser)
NM_153035.3(TCEANC2):c.407A>C (p.Gln136Pro)
NM_153035.3(TCEANC2):c.7A>G (p.Lys3Glu)	rs1255850946

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