List of variants in gene FRAS1 reported by Genetic Services Laboratory, University of Chicago

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.1710C>T (p.Pro570=)	rs17003124	0.00783
NM_025074.7(FRAS1):c.10598G>A (p.Arg3533Gln)	rs115878217	0.00648
NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln)	rs61729366	0.00592
NM_025074.7(FRAS1):c.10312G>A (p.Val3438Met)	rs34063631	0.00478
NM_025074.7(FRAS1):c.10149C>T (p.Thr3383=)	rs35321934	0.00379
NM_025074.7(FRAS1):c.6301C>T (p.His2101Tyr)	rs183398121	0.00302
NM_025074.7(FRAS1):c.4579C>T (p.Arg1527Trp)	rs1872267	0.00253
NM_025074.7(FRAS1):c.2861C>T (p.Thr954Met)	rs17003166	0.00252
NM_025074.7(FRAS1):c.10539A>G (p.Thr3513=)	rs199921300	0.00098
NM_025074.7(FRAS1):c.4095C>T (p.Ile1365=)	rs79869130	0.00088
NM_025074.7(FRAS1):c.9446C>T (p.Thr3149Met)	rs150680111	0.00080
NM_025074.7(FRAS1):c.9296G>A (p.Arg3099Gln)	rs149692526	0.00071
NM_025074.7(FRAS1):c.6939C>T (p.Pro2313=)	rs150936204	0.00052
NM_025074.7(FRAS1):c.1607A>G (p.His536Arg)	rs193245098	0.00048
NM_025074.7(FRAS1):c.11871G>A (p.Arg3957=)	rs367585112	0.00019
NM_025074.7(FRAS1):c.9356A>G (p.Asn3119Ser)	rs191105001	0.00016
NM_025074.7(FRAS1):c.1535-4G>A	rs749569960	0.00011
NM_025074.7(FRAS1):c.3059G>A (p.Arg1020His)	rs773906563	0.00005
NM_025074.7(FRAS1):c.4807C>T (p.Arg1603Trp)	rs961911715	0.00005
NM_025074.7(FRAS1):c.11695C>T (p.Leu3899=)	rs367723684	0.00002
NM_025074.7(FRAS1):c.1687C>G (p.Gln563Glu)	rs1254192090	0.00001
NM_025074.7(FRAS1):c.2046G>A (p.Val682=)	rs764188507	0.00001
NM_025074.7(FRAS1):c.2719C>T (p.Gln907Ter)	rs755750961	0.00001
NM_025074.7(FRAS1):c.4098C>T (p.Ile1366=)	rs1027609786	0.00001
NM_025074.7(FRAS1):c.1882C>A (p.Pro628Thr)	rs199542867
NM_025074.7(FRAS1):c.7029+9A>C	rs188606284
NM_025074.7(FRAS1):c.7522+1G>T	rs730882180

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