"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SLC17A4"[g - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2352092	NM_005495.3(SLC17A4):c.37G>T (p.Asp13Tyr)	SLC17A1, SLC17A4 (D13Y)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2352093	NM_005495.3(SLC17A4):c.39C>A (p.Asp13Glu)	SLC17A1, SLC17A4 (D13E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity