List of variants in gene TUBB4A 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006087.4(TUBB4A):c.1329G>A (p.Val443=)	rs751733505	0.00001
NM_006087.4(TUBB4A):c.278-6C>T	rs761298089	0.00001
NM_006087.4(TUBB4A):c.327C>T (p.Gly109=)	rs774127285	0.00001
NM_006087.4(TUBB4A):c.777C>G (p.Pro259=)	rs773226267	0.00001
NM_001289129.2(TUBB4A):c.-53G>T
NM_001289129.2(TUBB4A):c.-75G>C
NM_006087.4(TUBB4A):c.1276C>G (p.Gln426Glu)
NM_006087.4(TUBB4A):c.256C>T (p.Arg86Trp)	rs2145259455
NM_006087.4(TUBB4A):c.260C>T (p.Pro87Leu)
NM_006087.4(TUBB4A):c.292G>C (p.Gly98Arg)	rs1255699601
NM_006087.4(TUBB4A):c.447G>A (p.Thr149=)
NM_006087.4(TUBB4A):c.538G>A (p.Val180Met)	rs1064797231
NM_006087.4(TUBB4A):c.722G>A (p.Arg241His)
NM_006087.4(TUBB4A):c.79G>C (p.Glu27Gln)

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