List of variants in gene DOK7 reported as likely benign 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_173660.5(DOK7):c.134C>T (p.Ser45Leu)	rs62272670	0.00470
NM_001301071.2(DOK7):c.1599G>A (p.Ser533=)	rs115742102	0.00363
NM_173660.5(DOK7):c.1278C>T (p.Pro426=)	rs139468087	0.00181
NM_173660.5(DOK7):c.1507C>A (p.Pro503Thr)	rs184556570	0.00117
NM_173660.5(DOK7):c.831C>T (p.Ala277=)	rs150549589	0.00113
NM_173660.5(DOK7):c.282C>T (p.His94=)	rs377025553	0.00022
NM_173660.5(DOK7):c.846C>T (p.Thr282=)	rs141147662	0.00022
NM_173660.5(DOK7):c.1320C>T (p.Ala440=)	rs368868378	0.00019
NM_173660.5(DOK7):c.480C>T (p.Tyr160=)	rs550024569	0.00009
NM_173660.5(DOK7):c.1191G>C (p.Val397=)	rs781489489	0.00001
NM_173660.5(DOK7):c.1443C>T (p.His481=)	rs749462644	0.00001
NM_001301071.2(DOK7):c.1541-5dup
NM_001301071.2(DOK7):c.1554C>G (p.Pro518=)
NM_001301071.2(DOK7):c.1587G>T (p.Pro529=)
NM_001301071.2(DOK7):c.1596G>A (p.Glu532=)
NM_001301071.2(DOK7):c.1710C>T (p.Leu570=)
NM_173660.5(DOK7):c.954C>A (p.Pro318=)

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