Related gene-specific medical variations for Gene (Select 51379) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3077530	NM_015986.4(CRLF3):c.24G>T (p.Glu8Asp)	CRLF3, LOC121587585 (E8D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547292	NM_015986.4(CRLF3):c.34C>G (p.Leu12Val)	CRLF3, LOC121587585 (L12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 815922	GRCh37/hg19 17q11.2(chr17:28952286-29150025)x3	CRLF3	Copy number gain	not provided	GUncertain significance
Select item 564424	GRCh37/hg19 17q11.2(chr17:28952286-29121921)x3	CRLF3	Copy number gain	not provided	GUncertain significance

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