List of variants in gene RANBP2 reported by Fulgent Genetics, Fulgent Genetics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006267.5(RANBP2):c.6609G>A (p.Ala2203=)	rs60199637	0.04502
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=)	rs140275032	0.00951
NM_006267.5(RANBP2):c.1632-16T>C	rs147266881	0.00948
NM_006267.5(RANBP2):c.1087C>T (p.Arg363Cys)	rs149207118	0.00617
NM_006267.5(RANBP2):c.-41G>T	rs372373398	0.00331
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile)	rs140280672	0.00061
NM_006267.5(RANBP2):c.7340C>T (p.Ser2447Phe)	rs200750445	0.00022
NM_006267.5(RANBP2):c.1957A>G (p.Thr653Ala)	rs149578420	0.00018
NM_006267.5(RANBP2):c.1535C>T (p.Pro512Leu)	rs377029115	0.00014
NM_006267.5(RANBP2):c.8369T>A (p.Phe2790Tyr)	rs142150663	0.00003
NM_006267.5(RANBP2):c.4331C>T (p.Ala1444Val)	rs150309568	0.00002
NM_006267.5(RANBP2):c.1754C>T (p.Thr585Met)	rs121434502	0.00001
NM_006267.5(RANBP2):c.5570A>G (p.Gln1857Arg)	rs2149279328
NM_006267.5(RANBP2):c.7474A>G (p.Thr2492Ala)	rs2693103

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