List of variants in gene combination DEAF1, LOC126861109 studied for not specified

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_021008.4(DEAF1):c.1401G>A (p.Ala467=)	rs35303725	0.01277
NM_021008.4(DEAF1):c.1320G>A (p.Ala440=)	rs187523180	0.00007
NM_021008.4(DEAF1):c.1348C>T (p.Pro450Ser)	rs374222357	0.00003
NM_021008.4(DEAF1):c.1294A>C (p.Thr432Pro)	rs1352647775	0.00001
NM_021008.4(DEAF1):c.1350G>T (p.Pro450=)	rs764182783
NM_021008.4(DEAF1):c.1388T>C (p.Leu463Ser)	rs1554941501

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