List of variants in gene KIF1A reported as uncertain significance by Baylor Genetics

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001244008.2(KIF1A):c.1208-40G>A	rs375833834	0.00073
NM_001244008.2(KIF1A):c.4909G>A (p.Glu1637Lys)	rs377032453	0.00006
NM_001244008.2(KIF1A):c.4975G>A (p.Glu1659Lys)	rs764970503	0.00004
NM_001244008.2(KIF1A):c.4999G>A (p.Asp1667Asn)	rs754893576	0.00004
NM_001244008.2(KIF1A):c.850G>A (p.Ala284Thr)	rs756136593	0.00004
NM_001244008.2(KIF1A):c.2680G>A (p.Asp894Asn)	rs1064796756	0.00002
NM_001244008.2(KIF1A):c.3979G>A (p.Gly1327Arg)	rs879253904	0.00002
NM_001244008.2(KIF1A):c.482A>T (p.Lys161Met)	rs1011045689	0.00002
NM_001244008.2(KIF1A):c.1267G>A (p.Ala423Thr)	rs1345536541	0.00001
NM_001244008.2(KIF1A):c.4046T>C (p.Met1349Thr)	rs1045777400	0.00001
NM_001244008.2(KIF1A):c.4217G>A (p.Arg1406His)	rs755301795	0.00001
NM_001244008.2(KIF1A):c.1132C>T (p.Arg378Trp)	rs1438039466
NM_001244008.2(KIF1A):c.194T>C (p.Ile65Thr)	rs2055194876
NM_001244008.2(KIF1A):c.2022+3G>A	rs566702367
NM_001244008.2(KIF1A):c.2213A>G (p.Asn738Ser)	rs1559506707
NM_001244008.2(KIF1A):c.2445-3del
NM_001244008.2(KIF1A):c.2978-14T>G	rs964376899
NM_001244008.2(KIF1A):c.3221T>C (p.Leu1074Pro)	rs750268852
NM_001244008.2(KIF1A):c.364-3C>A	rs2055065906
NM_001244008.2(KIF1A):c.4255A>G (p.Ser1419Gly)	rs1388325896
NM_001244008.2(KIF1A):c.4753A>T (p.Met1585Leu)	rs1203273192
NM_001244008.2(KIF1A):c.4805C>G (p.Thr1602Ser)	rs1232607807
NM_001244008.2(KIF1A):c.5051A>G (p.His1684Arg)	rs2044948828
NM_001244008.2(KIF1A):c.5350AGG[1] (p.Arg1785del)	rs760590728
NM_001244008.2(KIF1A):c.647G>C (p.Arg216Pro)	rs672601368
NM_001244008.2(KIF1A):c.650C>T (p.Ser217Phe)	rs876661202
NM_001244008.2(KIF1A):c.947G>A (p.Arg316Gln)	rs749718096

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