List of variants in gene KRTAP24-1 reported as uncertain significance

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_001085455.3(KRTAP24-1):c.143C>T (p.Pro48Leu)	rs201007859	0.00023
NM_001085455.3(KRTAP24-1):c.272C>T (p.Ser91Phe)	rs368383552	0.00005
NM_001085455.3(KRTAP24-1):c.622T>C (p.Tyr208His)	rs529683700	0.00004
NM_001085455.3(KRTAP24-1):c.437G>A (p.Arg146His)	rs771391061	0.00001
NM_001085455.3(KRTAP24-1):c.739G>A (p.Gly247Ser)	rs1239261938	0.00001
NM_001085455.3(KRTAP24-1):c.17T>C (p.Met6Thr)
NM_001085455.3(KRTAP24-1):c.221C>T (p.Pro74Leu)
NM_001085455.3(KRTAP24-1):c.232C>A (p.Pro78Thr)
NM_001085455.3(KRTAP24-1):c.29G>T (p.Gly10Val)
NM_001085455.3(KRTAP24-1):c.535C>G (p.Gln179Glu)	rs1017568295
NM_001085455.3(KRTAP24-1):c.590G>A (p.Ser197Asn)
NM_001085455.3(KRTAP24-1):c.623A>T (p.Tyr208Phe)	rs1383405623
NM_001085455.3(KRTAP24-1):c.629A>G (p.Tyr210Cys)
NM_001085455.3(KRTAP24-1):c.643C>T (p.Pro215Ser)

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