List of variants in gene HOXB13 reported by Sema4, Sema4

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006361.6(HOXB13):c.735G>A (p.Lys245=)	rs138675188	0.00147
NM_006361.6(HOXB13):c.411C>T (p.Tyr137=)	rs377339084	0.00022
NM_006361.6(HOXB13):c.602-9G>A	rs148901331	0.00022
NM_006361.6(HOXB13):c.6G>A (p.Glu2=)	rs371544984	0.00015
NM_006361.6(HOXB13):c.634G>A (p.Ala212Thr)	rs145059285	0.00014
NM_006361.6(HOXB13):c.474G>A (p.Pro158=)	rs35033273	0.00013
NM_006361.6(HOXB13):c.610G>A (p.Gly204Arg)	rs1014715541	0.00003
NM_006361.6(HOXB13):c.686G>A (p.Arg229Gln)	rs936554882	0.00003
NM_006361.6(HOXB13):c.253G>A (p.Gly85Ser)	rs529392210	0.00001
NM_006361.6(HOXB13):c.258G>C (p.Gly86=)	rs754872559	0.00001
NM_006361.6(HOXB13):c.356A>T (p.Glu119Val)	rs1383196644	0.00001
NM_006361.6(HOXB13):c.195A>G (p.Pro65=)	rs1597934828
NM_006361.6(HOXB13):c.288G>A (p.Ser96=)	rs767708021
NM_006361.6(HOXB13):c.601+7C>G	rs752322954

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