List of variants in gene CDK13 reported by Fulgent Genetics, Fulgent 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003718.5(CDK13):c.1207C>T (p.Leu403Phe)	rs3735137	0.00138
NM_003718.5(CDK13):c.2180C>T (p.Thr727Ile)	rs140848307	0.00107
NM_003718.5(CDK13):c.3955G>A (p.Gly1319Ser)	rs147108931	0.00018
NM_003718.5(CDK13):c.1347G>T (p.Leu449=)	rs150303277	0.00014
NM_003718.5(CDK13):c.2149G>A (p.Gly717Arg)	rs1057519632
NM_003718.5(CDK13):c.2525A>G (p.Asn842Ser)	rs878853160

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