ClinVar for MedGen (Select 394510) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14315	NM_002386.4(MC1R):c.475C>A (p.Pro159Thr)	MC1R (P159T)	Single nucleotide variant (missense variant)	UV-induced skin damage, susceptibility to	Grisk factor
Select item 14314	NM_002386.4(MC1R):c.470C>T (p.Thr157Ile)	MC1R (T157I)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 5	GUncertain significance
Select item 14313	NM_002386.4(MC1R):c.437TCT[1] (p.Phe147del)	MC1R (F147del)	Microsatellite (inframe_deletion)	UV-induced skin damage, susceptibility to	Grisk factor

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