Related gene-specific medical variations for Gene (Select 641455) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309001	NM_001145442.1(POTEM):c.959T>C (p.Ile320Thr)	LOC100508046, POTEM (I320T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2387495	NM_001145442.1(POTEM):c.1021G>A (p.Ala341Thr)	LOC100508046, POTEM (A341T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2383962	NM_001145442.1(POTEM):c.1054G>A (p.Val352Ile)	LOC100508046, POTEM (V352I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2367059	NM_001145442.1(POTEM):c.920C>G (p.Thr307Ser)	LOC100508046, POTEM (T307S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2349482	NM_001145442.1(POTEM):c.984C>G (p.Asn328Lys)	LOC100508046, POTEM (N328K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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