List of variants in gene INTS1 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001080453.3(INTS1):c.6248T>G (p.Phe2083Cys)	rs201675191	0.00141
NM_001080453.3(INTS1):c.1568G>A (p.Arg523His)	rs374284848	0.00009
NM_001080453.3(INTS1):c.3335C>T (p.Ala1112Val)	rs778381554	0.00006
NM_001080453.3(INTS1):c.5561C>T (p.Ala1854Val)	rs373812497	0.00005
NM_001080453.3(INTS1):c.3091C>T (p.Arg1031Trp)	rs765667210	0.00002
NM_001080453.3(INTS1):c.1195G>A (p.Gly399Ser)	rs1439392344	0.00001
NM_001080453.3(INTS1):c.1137+4C>T
NM_001080453.3(INTS1):c.1145G>A (p.Arg382Gln)	rs1782994531
NM_001080453.3(INTS1):c.1823A>G (p.Tyr608Cys)
NM_001080453.3(INTS1):c.3772A>G (p.Met1258Val)
NM_001080453.3(INTS1):c.4570G>A (p.Val1524Ile)
NM_001080453.3(INTS1):c.4957G>T (p.Val1653Leu)	rs751579078
NM_001080453.3(INTS1):c.712C>T (p.Arg238Trp)

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