List of variants in gene RIMS1 reported by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_014989.7(RIMS1):c.1776G>A (p.Glu592=)	rs77121218	0.01826
NM_014989.7(RIMS1):c.438C>T (p.Arg146=)	rs142196418	0.00298
NM_014989.7(RIMS1):c.3465G>A (p.Ala1155=)	rs190562383	0.00108
NM_014989.7(RIMS1):c.4159C>T (p.Arg1387Trp)	rs201017334	0.00039
NM_014989.7(RIMS1):c.3703G>A (p.Gly1235Arg)	rs200637817	0.00033
NM_014989.7(RIMS1):c.3430C>T (p.Arg1144Ter)	rs202076893	0.00024
NM_014989.7(RIMS1):c.2894C>T (p.Pro965Leu)	rs752875047	0.00010
NM_014989.7(RIMS1):c.1723C>T (p.Arg575Trp)	rs767118962	0.00002
NM_014989.7(RIMS1):c.2708G>A (p.Arg903Gln)	rs776822598	0.00001
NM_014989.7(RIMS1):c.3281T>G (p.Leu1094Trp)	rs761114297	0.00001
NM_014989.7(RIMS1):c.1888C>T (p.Arg630Ter)
NM_014989.7(RIMS1):c.2333G>A (p.Arg778Gln)
NM_014989.7(RIMS1):c.2626C>A (p.Pro876Thr)
NM_014989.7(RIMS1):c.3959C>A (p.Ser1320Tyr)	rs140943787
NM_014989.7(RIMS1):c.4459C>T (p.Arg1487Ter)
NM_014989.7(RIMS1):c.812+10C>T

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