Related gene-specific medical variations for Gene (Select 64090) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280487	NM_022134.3(GAL3ST2):c.1008C>A (p.Asp336Glu)	GAL3ST2, LOC110599582 (D336E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280486	NM_022134.3(GAL3ST2):c.1019G>A (p.Arg340His)	GAL3ST2, LOC110599582 (R340H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280484	NM_022134.3(GAL3ST2):c.1022C>T (p.Pro341Leu)	GAL3ST2, LOC110599582 (P341L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097997	NM_022134.3(GAL3ST2):c.992A>C (p.His331Pro)	GAL3ST2, LOC110599582 (H331P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097990	NM_022134.3(GAL3ST2):c.1181C>G (p.Pro394Arg)	GAL3ST2, LOC110599582 (P394R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097989	NM_022134.3(GAL3ST2):c.1163A>C (p.Lys388Thr)	GAL3ST2, LOC110599582 (K388T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097988	NM_022134.3(GAL3ST2):c.1124A>G (p.Gln375Arg)	GAL3ST2, LOC110599582 (Q375R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097987	NM_022134.3(GAL3ST2):c.1059C>A (p.Asn353Lys)	GAL3ST2, LOC110599582 (N353K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097986	NM_022134.3(GAL3ST2):c.1040C>T (p.Ala347Val)	GAL3ST2, LOC110599582 (A347V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454766	NM_022134.3(GAL3ST2):c.1157C>G (p.Pro386Arg)	GAL3ST2, LOC110599582 (P386R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269016	NM_022134.3(GAL3ST2):c.998A>T (p.Gln333Leu)	GAL3ST2, LOC110599582 (Q333L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245786	NM_022134.3(GAL3ST2):c.1129A>C (p.Met377Leu)	GAL3ST2, LOC110599582 (M377L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance