List of variants in gene KIAA1549 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001164665.2(KIAA1549):c.1982A>T (p.Gln661Leu)	rs375009657	0.00006
NM_001164665.2(KIAA1549):c.2315C>A (p.Pro772His)
NM_001164665.2(KIAA1549):c.4099G>A (p.Asp1367Asn)
NM_001164665.2(KIAA1549):c.4139C>T (p.Pro1380Leu)
NM_001164665.2(KIAA1549):c.4989T>G (p.Tyr1663Ter)	rs1584710731
NM_001164665.2(KIAA1549):c.5079C>A (p.Asp1693Glu)
NM_001164665.2(KIAA1549):c.676G>C (p.Ala226Pro)

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