"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "IGF2"[gene - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 729023	NM_000612.6(IGF2):c.381C>T (p.Arg127=)	IGF2, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1597228	NM_000612.6(IGF2):c.270C>T (p.Ser90=)	IGF2, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2071277	NM_000612.6(IGF2):c.138G>T (p.Gly46=)	IGF2, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2641354	NM_001042376.3(INS-IGF2):c.378T>G (p.Ala126=)	IGF2, INS-IGF2	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign

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