List of variants in gene RAB11FIP5 studied for not provided

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001371272.1(RAB11FIP5):c.235C>G (p.Pro79Ala)	rs116086108	0.00441
NM_001371272.1(RAB11FIP5):c.1568+8G>A	rs201414059	0.00313
NM_001371272.1(RAB11FIP5):c.1290G>A (p.Glu430=)	rs140983118	0.00201
NM_001371272.1(RAB11FIP5):c.3963C>T (p.Gly1321=)	rs149355459	0.00175
NM_001371272.1(RAB11FIP5):c.3592G>A (p.Val1198Met)	rs147740837	0.00082
NM_001371272.1(RAB11FIP5):c.1435C>T (p.Arg479Cys)	rs143156025	0.00076
NM_001371272.1(RAB11FIP5):c.3909G>A (p.Arg1303=)	rs200288307	0.00063
NM_001371272.1(RAB11FIP5):c.1478C>T (p.Ala493Val)	rs200150559	0.00034
NM_001371272.1(RAB11FIP5):c.309C>T (p.Ala103=)	rs374744842	0.00024
NM_001371272.1(RAB11FIP5):c.3819C>T (p.His1273=)	rs201443945	0.00011
NM_001371272.1(RAB11FIP5):c.192C>T (p.His64=)	rs561110981	0.00004
NM_001371272.1(RAB11FIP5):c.3869G>A (p.Arg1290Gln)	rs868507082	0.00001
NM_001371272.1(RAB11FIP5):c.408C>T (p.Gly136=)	rs1574308919	0.00001
NM_001371272.1(RAB11FIP5):c.306C>T (p.Ser102=)	rs755850240
NM_001371272.1(RAB11FIP5):c.3873C>T (p.Asp1291=)	rs17008666

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