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Gene: SSBP1 & Disease: CORD2, 5 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
977502	SSBP1	c.113G>A	p.Arg38Gln (p.R38Q)	NM_003143.3 M	SNV	P	2 +	3
	SSBP1	c.113G>A	p.Arg38Gln (p.R38Q)	NM_001256510.1	SNV	P	2 +	3
	SSBP1	c.113G>A	p.Arg38Gln (p.R38Q)	NM_001256511.1	SNV	P	2 +	3
	SSBP1	c.113G>A	p.Arg38Gln (p.R38Q)	NM_001256512.1	SNV	P	2 +	3
	SSBP1	c.113G>A	p.Arg38Gln (p.R38Q)	NM_001256513.1	SNV	P	2 +	3

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