Related gene-specific medical variations for Gene (Select 149628) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3150239	NM_152501.5(PYHIN1):c.370C>G (p.Arg124Gly)	LOC126805885, PYHIN1 (R115G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150238	NM_152501.5(PYHIN1):c.349C>T (p.Pro117Ser)	LOC126805885, PYHIN1 (P108S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407051	NM_152501.5(PYHIN1):c.524G>T (p.Arg175Leu)	LOC126805885, PYHIN1 (R175L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364090	NM_152501.5(PYHIN1):c.521G>A (p.Gly174Asp)	LOC126805885, PYHIN1 (G174D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347396	NM_152501.5(PYHIN1):c.506C>T (p.Thr169Met)	LOC126805885, PYHIN1 (T169M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2345223	NM_152501.5(PYHIN1):c.547T>C (p.Ser183Pro)	LOC126805885, PYHIN1 (S183P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216902	NM_152501.5(PYHIN1):c.423A>C (p.Lys141Asn)	LOC126805885, PYHIN1 (K141N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161854	NM_152501.5(PYHIN1):c.602G>A (p.Arg201His)	PYHIN1 (R192H +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar