Related gene-specific medical variations for Gene (Select 8527) - ClinVar - NCBI

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Links from Gene

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081892	NM_152879.3(DGKD):c.28C>G (p.Pro10Ala)	DGKD, LOC129935890 (P10A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601256	NM_152879.3(DGKD):c.44C>G (p.Pro15Arg)	DGKD, LOC129935890 (P15R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480360	NM_152879.3(DGKD):c.49C>G (p.Pro17Ala)	DGKD, LOC129935890 (P17A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464000	NM_152879.3(DGKD):c.49C>A (p.Pro17Thr)	DGKD, LOC129935890 (P17T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462114	NM_152879.3(DGKD):c.98C>T (p.Pro33Leu)	DGKD, LOC129935890 (P33L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333294	NM_152879.3(DGKD):c.25C>G (p.Pro9Ala)	DGKD, LOC129935890 (P9A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206726	NM_152879.3(DGKD):c.23C>T (p.Pro8Leu)	DGKD, LOC129935890 (P8L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 753345	NM_152879.3(DGKD):c.24T>A (p.Pro8=)	LOC129935890, DGKD	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 743421	NM_152879.3(DGKD):c.51G>A (p.Pro17=)	DGKD, LOC129935890	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 734116	NM_152879.3(DGKD):c.34C>A (p.Pro12Thr)	LOC129935890, DGKD (P12T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 92031	NM_152879.3(DGKD):c.472G>A (p.Asp158Asn)	DGKD (D158N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance