Related gene-specific medical variations for Gene (Select 5646) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3238621	NM_002771.4(PRSS3):c.74T>C (p.Val25Ala)	PRSS3, UBE2R2-AS1 (V18A +2 more)	Single nucleotide variant (missense variant +1 more)	Thyroiditis	GUncertain significance
Select item 2786908	NM_002771.4(PRSS3):c.391A>G (p.Thr131Ala)	PRSS3, UBE2R2-AS1 (T131A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1294450	NM_007343.4(PRSS3):c.-285+290C>A	UBE2R2-AS1, PRSS3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291262	NM_002771.4(PRSS3):c.200+112A>G	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280871	NM_007343.4(PRSS3):c.-285+23G>T	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271011	NM_001197097.3(PRSS3):c.51G>A (p.Ala17=)	PRSS3, UBE2R2-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1263618	NM_002771.4(PRSS3):c.200+256A>T	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259461	NM_007343.4(PRSS3):c.-285+120G>C	PRSS3, UBE2R2-AS1 (G5A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1245449	NM_002771.4(PRSS3):c.201-66G>T	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239378	NM_002771.4(PRSS3):c.592-188T>C	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237663	NM_002771.4(PRSS3):c.201-66G>A	PRSS3, UBE2R2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225003	NM_002771.4(PRSS3):c.91GAG[1] (p.Glu32del)	PRSS3, UBE2R2-AS1 (E25del +2 more)	Microsatellite (inframe_deletion +1 more)	not provided	GBenign